| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55201065_55201193del | CA2580611830 | EGFR | c.2788-123_2793del c.900-4282_900-4154del n.691-123_696del n.493_621del c.2947-123_2952del c.*28+28137_*28+28265del (n.*28+28137_*28+28265del) c.2812-123_2817del c.2146-123_2151del | |
| 7 | g.55201167G>A | CA2714961098 | EGFR | c.2788-21G>A (n.2788-21G>A) c.900-4180G>A n.691-21G>A n.595G>A c.2947-21G>A (n.2947-21G>A) c.*28+28239G>A (n.*28+28239G>A) c.2812-21G>A (n.2812-21G>A) c.2146-21G>A (n.2146-21G>A) | dbSNP |
| 7 | g.55201167G>C | CA2714961099 | EGFR | c.2788-21G>C (n.2788-21G>C) c.900-4180G>C n.691-21G>C n.595G>C c.2947-21G>C (n.2947-21G>C) c.*28+28239G>C (n.*28+28239G>C) c.2812-21G>C (n.2812-21G>C) c.2146-21G>C (n.2146-21G>C) | dbSNP |
| 7 | g.55201167G>T | CA2714961097 | EGFR | c.2788-21G>T (n.2788-21G>T) c.900-4180G>T n.691-21G>T n.595G>T c.2947-21G>T (n.2947-21G>T) c.*28+28239G>T (n.*28+28239G>T) c.2812-21G>T (n.2812-21G>T) c.2146-21G>T (n.2146-21G>T) | dbSNP |
| 7 | g.55201168C>A | CA2714961102 | EGFR | c.2788-20C>A (n.2788-20C>A) c.900-4179C>A n.691-20C>A n.596C>A c.2947-20C>A (n.2947-20C>A) c.*28+28240C>A (n.*28+28240C>A) c.2812-20C>A (n.2812-20C>A) c.2146-20C>A (n.2146-20C>A) | dbSNP |
| 7 | g.55201168C>G | CA2714961101 | EGFR | c.2788-20C>G (n.2788-20C>G) c.900-4179C>G n.691-20C>G n.596C>G c.2947-20C>G (n.2947-20C>G) c.*28+28240C>G (n.*28+28240C>G) c.2812-20C>G (n.2812-20C>G) c.2146-20C>G (n.2146-20C>G) | dbSNP |
| 7 | g.55201168C>T | CA2714961100 | EGFR | c.2788-20C>T (n.2788-20C>T) c.900-4179C>T n.691-20C>T n.596C>T c.2947-20C>T (n.2947-20C>T) c.*28+28240C>T (n.*28+28240C>T) c.2812-20C>T (n.2812-20C>T) c.2146-20C>T (n.2146-20C>T) | dbSNP |
| 7 | g.55201169C>A | CA839817020 | EGFR | c.2788-19C>A (n.2788-19C>A) c.900-4178C>A n.691-19C>A n.597C>A c.2947-19C>A (n.2947-19C>A) c.*28+28241C>A (n.*28+28241C>A) c.2812-19C>A (n.2812-19C>A) c.2146-19C>A (n.2146-19C>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201169C= | CA1708928402 | EGFR | c.2788-19C= (n.2788-19C=) c.900-4178C= n.691-19C= n.597C= c.2947-19C= (n.2947-19C=) c.*28+28241C= (n.*28+28241C=) c.2812-19C= (n.2812-19C=) c.2146-19C= (n.2146-19C=) | |
| 7 | g.55201169C>T | CA4266222 | EGFR | c.2788-19C>T (n.2788-19C>T) c.900-4178C>T n.691-19C>T n.597C>T c.2947-19C>T (n.2947-19C>T) c.*28+28241C>T (n.*28+28241C>T) c.2812-19C>T (n.2812-19C>T) c.2146-19C>T (n.2146-19C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201170T>A | CA2714961105 | EGFR | c.2788-18T>A (n.2788-18T>A) c.900-4177T>A n.691-18T>A n.598T>A c.2947-18T>A (n.2947-18T>A) c.*28+28242T>A (n.*28+28242T>A) c.2812-18T>A (n.2812-18T>A) c.2146-18T>A (n.2146-18T>A) | dbSNP |
| 7 | g.55201170T>C | CA2714961104 | EGFR | c.2788-18T>C (n.2788-18T>C) c.900-4177T>C n.691-18T>C n.598T>C c.2947-18T>C (n.2947-18T>C) c.*28+28242T>C (n.*28+28242T>C) c.2812-18T>C (n.2812-18T>C) c.2146-18T>C (n.2146-18T>C) | dbSNP |
| 7 | g.55201171C>A | CA2714507208 | EGFR | c.2788-17C>A (n.2788-17C>A) c.900-4176C>A n.691-17C>A n.599C>A c.2947-17C>A (n.2947-17C>A) c.*28+28243C>A (n.*28+28243C>A) c.2812-17C>A (n.2812-17C>A) c.2146-17C>A (n.2146-17C>A) | dbSNP |
| 7 | g.55201171C= | CA1708928403 | EGFR | c.2788-17C= (n.2788-17C=) c.900-4176C= n.691-17C= n.599C= c.2947-17C= (n.2947-17C=) c.*28+28243C= (n.*28+28243C=) c.2812-17C= (n.2812-17C=) c.2146-17C= (n.2146-17C=) | |
| 7 | g.55201171C>G | CA4266224 | EGFR | c.2788-17C>G (n.2788-17C>G) c.900-4176C>G n.691-17C>G n.599C>G c.2947-17C>G (n.2947-17C>G) c.*28+28243C>G (n.*28+28243C>G) c.2812-17C>G (n.2812-17C>G) c.2146-17C>G (n.2146-17C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201171C>T | CA4266223 | EGFR | c.2788-17C>T (n.2788-17C>T) c.900-4176C>T n.691-17C>T n.599C>T c.2947-17C>T (n.2947-17C>T) c.*28+28243C>T (n.*28+28243C>T) c.2812-17C>T (n.2812-17C>T) c.2146-17C>T (n.2146-17C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201172A>C | CA2714961110 | EGFR | c.2788-16A>C (n.2788-16A>C) c.900-4175A>C n.691-16A>C n.600A>C c.2947-16A>C (n.2947-16A>C) c.*28+28244A>C (n.*28+28244A>C) c.2812-16A>C (n.2812-16A>C) c.2146-16A>C (n.2146-16A>C) | dbSNP |
| 7 | g.55201172A>T | CA2714961111 | EGFR | c.2788-16A>T (n.2788-16A>T) c.900-4175A>T n.691-16A>T n.600A>T c.2947-16A>T (n.2947-16A>T) c.*28+28244A>T (n.*28+28244A>T) c.2812-16A>T (n.2812-16A>T) c.2146-16A>T (n.2146-16A>T) | dbSNP |
| 7 | g.55201175dup | CA2578893675 | EGFR | c.2788-13dup (n.2788-13dup) c.900-4172dup n.691-13dup n.603dup c.2947-13dup (n.2947-13dup) c.*28+28247dup (n.*28+28247dup) c.2812-13dup (n.2812-13dup) c.2146-13dup (n.2146-13dup) | |
| 7 | g.55201173A>C | CA2714961115 | EGFR | c.2788-15A>C (n.2788-15A>C) c.900-4174A>C n.691-15A>C n.601A>C c.2947-15A>C (n.2947-15A>C) c.*28+28245A>C (n.*28+28245A>C) c.2812-15A>C (n.2812-15A>C) c.2146-15A>C (n.2146-15A>C) | dbSNP |
| 7 | g.55201173A>T | CA2714961114 | EGFR | c.2788-15A>T (n.2788-15A>T) c.900-4174A>T n.691-15A>T n.601A>T c.2947-15A>T (n.2947-15A>T) c.*28+28245A>T (n.*28+28245A>T) c.2812-15A>T (n.2812-15A>T) c.2146-15A>T (n.2146-15A>T) | dbSNP |
| 7 | g.55201174A>T | CA2714961117 | EGFR | c.2788-14A>T (n.2788-14A>T) c.900-4173A>T n.691-14A>T n.602A>T c.2947-14A>T (n.2947-14A>T) c.*28+28246A>T (n.*28+28246A>T) c.2812-14A>T (n.2812-14A>T) c.2146-14A>T (n.2146-14A>T) | dbSNP |
| 7 | g.55201175A>C | CA2714961123 | EGFR | c.2788-13A>C (n.2788-13A>C) c.900-4172A>C n.691-13A>C n.603A>C c.2947-13A>C (n.2947-13A>C) c.*28+28247A>C (n.*28+28247A>C) c.2812-13A>C (n.2812-13A>C) c.2146-13A>C (n.2146-13A>C) | dbSNP |
| 7 | g.55201175A>G | CA2714961121 | EGFR | c.2788-13A>G (n.2788-13A>G) c.900-4172A>G n.691-13A>G n.603A>G c.2947-13A>G (n.2947-13A>G) c.*28+28247A>G (n.*28+28247A>G) c.2812-13A>G (n.2812-13A>G) c.2146-13A>G (n.2146-13A>G) | dbSNP |
| 7 | g.55201175A>T | CA2714961119 | EGFR | c.2788-13A>T (n.2788-13A>T) c.900-4172A>T n.691-13A>T n.603A>T c.2947-13A>T (n.2947-13A>T) c.*28+28247A>T (n.*28+28247A>T) c.2812-13A>T (n.2812-13A>T) c.2146-13A>T (n.2146-13A>T) | dbSNP |
| 7 | g.55201176T>A | CA2714961126 | EGFR | c.2788-12T>A (n.2788-12T>A) c.900-4171T>A n.691-12T>A n.604T>A c.2947-12T>A (n.2947-12T>A) c.*28+28248T>A (n.*28+28248T>A) c.2812-12T>A (n.2812-12T>A) c.2146-12T>A (n.2146-12T>A) | dbSNP |
| 7 | g.55201179_55201180del | CA2580615891 | EGFR | c.2788-9_2788-8del (n.2788-9_2788-8del) c.900-4168_900-4167del n.691-9_691-8del n.607_608del c.2947-9_2947-8del (n.2947-9_2947-8del) c.*28+28251_*28+28252del (n.*28+28251_*28+28252del) c.2812-9_2812-8del (n.2812-9_2812-8del) c.2146-9_2146-8del (n.2146-9_2146-8del) | ClinVar dbSNP |
| 7 | g.55201177C>A | CA2714961128 | EGFR | c.2788-11C>A (n.2788-11C>A) c.900-4170C>A n.691-11C>A n.605C>A c.2947-11C>A (n.2947-11C>A) c.*28+28249C>A (n.*28+28249C>A) c.2812-11C>A (n.2812-11C>A) c.2146-11C>A (n.2146-11C>A) | dbSNP |
| 7 | g.55201177C>G | CA2714961129 | EGFR | c.2788-11C>G (n.2788-11C>G) c.900-4170C>G n.691-11C>G n.605C>G c.2947-11C>G (n.2947-11C>G) c.*28+28249C>G (n.*28+28249C>G) c.2812-11C>G (n.2812-11C>G) c.2146-11C>G (n.2146-11C>G) | dbSNP |
| 7 | g.55201177C>T | CA2714961132 | EGFR | c.2788-11C>T (n.2788-11C>T) c.900-4170C>T n.691-11C>T n.605C>T c.2947-11C>T (n.2947-11C>T) c.*28+28249C>T (n.*28+28249C>T) c.2812-11C>T (n.2812-11C>T) c.2146-11C>T (n.2146-11C>T) | dbSNP |
| 7 | g.55201178T>C | CA2714961136 | EGFR | c.2788-10T>C (n.2788-10T>C) c.900-4169T>C n.691-10T>C n.606T>C c.2947-10T>C (n.2947-10T>C) c.*28+28250T>C (n.*28+28250T>C) c.2812-10T>C (n.2812-10T>C) c.2146-10T>C (n.2146-10T>C) | dbSNP |
| 7 | g.55201179C>A | CA2714508307 | EGFR | c.2788-9C>A (n.2788-9C>A) c.900-4168C>A n.691-9C>A n.607C>A c.2947-9C>A (n.2947-9C>A) c.*28+28251C>A (n.*28+28251C>A) c.2812-9C>A (n.2812-9C>A) c.2146-9C>A (n.2146-9C>A) | dbSNP |
| 7 | g.55201179C= | CA1708928404 | EGFR | c.2788-9C= (n.2788-9C=) c.900-4168C= n.691-9C= n.607C= c.2947-9C= (n.2947-9C=) c.*28+28251C= (n.*28+28251C=) c.2812-9C= (n.2812-9C=) c.2146-9C= (n.2146-9C=) | |
| 7 | g.55201179C>G | CA2714508306 | EGFR | c.2788-9C>G (n.2788-9C>G) c.900-4168C>G n.691-9C>G n.607C>G c.2947-9C>G (n.2947-9C>G) c.*28+28251C>G (n.*28+28251C>G) c.2812-9C>G (n.2812-9C>G) c.2146-9C>G (n.2146-9C>G) | dbSNP |
| 7 | g.55201179C>T | CA4266225 | EGFR | c.2788-9C>T (n.2788-9C>T) c.900-4168C>T n.691-9C>T n.607C>T c.2947-9C>T (n.2947-9C>T) c.*28+28251C>T (n.*28+28251C>T) c.2812-9C>T (n.2812-9C>T) c.2146-9C>T (n.2146-9C>T) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 7 | g.55201180T>A | CA2714605807 | EGFR | c.2788-8T>A (n.2788-8T>A) c.900-4167T>A n.691-8T>A n.608T>A c.2947-8T>A (n.2947-8T>A) c.*28+28252T>A (n.*28+28252T>A) c.2812-8T>A (n.2812-8T>A) c.2146-8T>A (n.2146-8T>A) | dbSNP |
| 7 | g.55201180T>C | CA1101539163 | EGFR | c.2788-8T>C (n.2788-8T>C) c.900-4167T>C n.691-8T>C n.608T>C c.2947-8T>C (n.2947-8T>C) c.*28+28252T>C (n.*28+28252T>C) c.2812-8T>C (n.2812-8T>C) c.2146-8T>C (n.2146-8T>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201180T>G | CA2714605808 | EGFR | c.2788-8T>G (n.2788-8T>G) c.900-4167T>G n.691-8T>G n.608T>G c.2947-8T>G (n.2947-8T>G) c.*28+28252T>G (n.*28+28252T>G) c.2812-8T>G (n.2812-8T>G) c.2146-8T>G (n.2146-8T>G) | dbSNP |
| 7 | g.55201180T= | CA1708928405 | EGFR | c.2788-8T= (n.2788-8T=) c.900-4167T= n.691-8T= n.608T= c.2947-8T= (n.2947-8T=) c.*28+28252T= (n.*28+28252T=) c.2812-8T= (n.2812-8T=) c.2146-8T= (n.2146-8T=) | |
| 7 | g.55201181G>A | CA2714961142 | EGFR | c.2788-7G>A (n.2788-7G>A) c.900-4166G>A n.691-7G>A n.609G>A c.2947-7G>A (n.2947-7G>A) c.*28+28253G>A (n.*28+28253G>A) c.2812-7G>A (n.2812-7G>A) c.2146-7G>A (n.2146-7G>A) | dbSNP |
| 7 | g.55201181G>C | CA2714961148 | EGFR | c.2788-7G>C (n.2788-7G>C) c.900-4166G>C n.691-7G>C n.609G>C c.2947-7G>C (n.2947-7G>C) c.*28+28253G>C (n.*28+28253G>C) c.2812-7G>C (n.2812-7G>C) c.2146-7G>C (n.2146-7G>C) | dbSNP |
| 7 | g.55201181G>T | CA2714961139 | EGFR | c.2788-7G>T (n.2788-7G>T) c.900-4166G>T n.691-7G>T n.609G>T c.2947-7G>T (n.2947-7G>T) c.*28+28253G>T (n.*28+28253G>T) c.2812-7G>T (n.2812-7G>T) c.2146-7G>T (n.2146-7G>T) | dbSNP |
| 7 | g.55201182C>A | CA2714961150 | EGFR | c.2788-6C>A (n.2788-6C>A) c.900-4165C>A n.691-6C>A n.610C>A c.2947-6C>A (n.2947-6C>A) c.*28+28254C>A (n.*28+28254C>A) c.2812-6C>A (n.2812-6C>A) c.2146-6C>A (n.2146-6C>A) | dbSNP |
| 7 | g.55201182C>G | CA2714961154 | EGFR | c.2788-6C>G (n.2788-6C>G) c.900-4165C>G n.691-6C>G n.610C>G c.2947-6C>G (n.2947-6C>G) c.*28+28254C>G (n.*28+28254C>G) c.2812-6C>G (n.2812-6C>G) c.2146-6C>G (n.2146-6C>G) | dbSNP |
| 7 | g.55201182C>T | CA2714961152 | EGFR | c.2788-6C>T (n.2788-6C>T) c.900-4165C>T n.691-6C>T n.610C>T c.2947-6C>T (n.2947-6C>T) c.*28+28254C>T (n.*28+28254C>T) c.2812-6C>T (n.2812-6C>T) c.2146-6C>T (n.2146-6C>T) | dbSNP |
| 7 | g.55201183A= | CA1708928406 | EGFR | c.2788-5A= (n.2788-5A=) c.900-4164A= n.691-5A= n.611A= c.2947-5A= (n.2947-5A=) c.*28+28255A= (n.*28+28255A=) c.2812-5A= (n.2812-5A=) c.2146-5A= (n.2146-5A=) | |
| 7 | g.55201183A>G | CA4266226 | EGFR | c.2788-5A>G (n.2788-5A>G) c.900-4164A>G n.691-5A>G n.611A>G c.2947-5A>G (n.2947-5A>G) c.*28+28255A>G (n.*28+28255A>G) c.2812-5A>G (n.2812-5A>G) c.2146-5A>G (n.2146-5A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201184C>A | CA2573142279 | EGFR | c.2788-4C>A (n.2788-4C>A) c.900-4163C>A n.691-4C>A n.612C>A c.2947-4C>A (n.2947-4C>A) c.*28+28256C>A (n.*28+28256C>A) c.2812-4C>A (n.2812-4C>A) c.2146-4C>A (n.2146-4C>A) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201184C>G | CA2682856322 | EGFR | c.2788-4C>G (n.2788-4C>G) c.900-4163C>G n.691-4C>G n.612C>G c.2947-4C>G (n.2947-4C>G) c.*28+28256C>G (n.*28+28256C>G) c.2812-4C>G (n.2812-4C>G) c.2146-4C>G (n.2146-4C>G) | gnomAD v4 |
| 7 | g.55201184C>T | CA2573142280 | EGFR | c.2788-4C>T (n.2788-4C>T) c.900-4163C>T n.691-4C>T n.612C>T c.2947-4C>T (n.2947-4C>T) c.*28+28256C>T (n.*28+28256C>T) c.2812-4C>T (n.2812-4C>T) c.2146-4C>T (n.2146-4C>T) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201185C>A | CA2714961182 | EGFR | c.2788-3C>A (n.2788-3C>A) c.900-4162C>A n.691-3C>A n.613C>A c.2947-3C>A (n.2947-3C>A) c.*28+28257C>A (n.*28+28257C>A) c.2812-3C>A (n.2812-3C>A) c.2146-3C>A (n.2146-3C>A) | dbSNP |
| 7 | g.55201185C>G | CA2714961180 | EGFR | c.2788-3C>G (n.2788-3C>G) c.900-4162C>G n.691-3C>G n.613C>G c.2947-3C>G (n.2947-3C>G) c.*28+28257C>G (n.*28+28257C>G) c.2812-3C>G (n.2812-3C>G) c.2146-3C>G (n.2146-3C>G) | dbSNP |
| 7 | g.55201185C>T | CA2714961178 | EGFR | c.2788-3C>T (n.2788-3C>T) c.900-4162C>T n.691-3C>T n.613C>T c.2947-3C>T (n.2947-3C>T) c.*28+28257C>T (n.*28+28257C>T) c.2812-3C>T (n.2812-3C>T) c.2146-3C>T (n.2146-3C>T) | dbSNP |
| 7 | g.55201186A>C | CA367582325 | EGFR | c.2788-2A>C (n.2788-2A>C) c.900-4161A>C n.691-2A>C n.614A>C c.2947-2A>C (n.2947-2A>C) c.*28+28258A>C (n.*28+28258A>C) c.2812-2A>C (n.2812-2A>C) c.2146-2A>C (n.2146-2A>C) | |
| 7 | g.55201186A>G | CA367582327 | EGFR | c.2788-2A>G (n.2788-2A>G) c.900-4161A>G n.691-2A>G n.614A>G c.2947-2A>G (n.2947-2A>G) c.*28+28258A>G (n.*28+28258A>G) c.2812-2A>G (n.2812-2A>G) c.2146-2A>G (n.2146-2A>G) | ClinVar |
| 7 | g.55201186A>T | CA367582326 | EGFR | c.2788-2A>T (n.2788-2A>T) c.900-4161A>T n.691-2A>T n.614A>T c.2947-2A>T (n.2947-2A>T) c.*28+28258A>T (n.*28+28258A>T) c.2812-2A>T (n.2812-2A>T) c.2146-2A>T (n.2146-2A>T) | |
| 7 | g.55201186_55201187delinsAG | CA1708928407 | EGFR | c.2788-2_2788-1delinsAG (n.2788-2_2788-1delinsAG) c.900-4161_900-4160delinsAG n.691-2_691-1delinsAG n.614_615delinsAG c.2947-2_2947-1delinsAG (n.2947-2_2947-1delinsAG) c.*28+28258_*28+28259delinsAG (n.*28+28258_*28+28259delinsAG) c.2812-2_2812-1delinsAG (n.2812-2_2812-1delinsAG) c.2146-2_2146-1delinsAG (n.2146-2_2146-1delinsAG) | |
| 7 | g.55201187G>A | CA367582328 | EGFR | c.2788-1G>A (n.2788-1G>A) c.900-4160G>A n.691-1G>A n.615G>A c.2947-1G>A (n.2947-1G>A) c.*28+28259G>A (n.*28+28259G>A) c.2812-1G>A (n.2812-1G>A) c.2146-1G>A (n.2146-1G>A) | ClinVar dbSNP |
| 7 | g.55201187G>C | CA367582329 | EGFR | c.2788-1G>C (n.2788-1G>C) c.900-4160G>C n.691-1G>C n.615G>C c.2947-1G>C (n.2947-1G>C) c.*28+28259G>C (n.*28+28259G>C) c.2812-1G>C (n.2812-1G>C) c.2146-1G>C (n.2146-1G>C) | |
| 7 | g.55201187G= | CA1708928408 | EGFR | c.2788-1G= (n.2788-1G=) c.900-4160G= n.691-1G= n.615G= c.2947-1G= (n.2947-1G=) c.*28+28259G= (n.*28+28259G=) c.2812-1G= (n.2812-1G=) c.2146-1G= (n.2146-1G=) | |
| 7 | g.55201187G>T | CA367582330 | EGFR | c.2788-1G>T (n.2788-1G>T) c.900-4160G>T n.691-1G>T n.615G>T c.2947-1G>T (n.2947-1G>T) c.*28+28259G>T (n.*28+28259G>T) c.2812-1G>T (n.2812-1G>T) c.2146-1G>T (n.2146-1G>T) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201191dup | CA2714571749 | EGFR | c.2791dup c.900-4156dup n.694dup n.619dup c.2950dup c.*28+28263dup (n.*28+28263dup) c.2815dup c.2149dup | dbSNP |
| 7 | g.55201191del | CA645560282 | EGFR | c.2791del c.900-4156del n.694del n.619del c.2950del c.*28+28263del (n.*28+28263del) c.2815del c.2149del | dbSNP COSMIC |
| 7 | g.55201188G>A | CA367582331 | EGFR | c.2788G>A (p.Gly930Arg) c.900-4159G>A n.691G>A n.616G>A c.2947G>A (p.Gly983Arg) c.*28+28260G>A (n.*28+28260G>A) c.2812G>A (p.Gly938Arg) c.2146G>A (p.Gly716Arg) | dbSNP COSMIC |
| 7 | g.55201188G>C | CA367582332 | EGFR | c.2788G>C (p.Gly930Arg) c.900-4159G>C n.691G>C n.616G>C c.2947G>C (p.Gly983Arg) c.*28+28260G>C (n.*28+28260G>C) c.2812G>C (p.Gly938Arg) c.2146G>C (p.Gly716Arg) | dbSNP |
| 7 | g.55201188G>T | CA367582333 | EGFR | c.2788G>T (p.Gly930Trp) c.900-4159G>T n.691G>T n.616G>T c.2947G>T (p.Gly983Trp) c.*28+28260G>T (n.*28+28260G>T) c.2812G>T (p.Gly938Trp) c.2146G>T (p.Gly716Trp) | dbSNP |
| 7 | g.55201189G>A | CA367582334 | EGFR | c.2789G>A (p.Gly930Glu) c.900-4158G>A n.692G>A n.617G>A c.2948G>A (p.Gly983Glu) c.*28+28261G>A (n.*28+28261G>A) c.2813G>A (p.Gly938Glu) c.2147G>A (p.Gly716Glu) | dbSNP gnomAD v4 |
| 7 | g.55201189G>C | CA367582335 | EGFR | c.2789G>C (p.Gly930Ala) c.900-4158G>C n.692G>C n.617G>C c.2948G>C (p.Gly983Ala) c.*28+28261G>C (n.*28+28261G>C) c.2813G>C (p.Gly938Ala) c.2147G>C (p.Gly716Ala) | dbSNP |
| 7 | g.55201189G>T | CA367582336 | EGFR | c.2789G>T (p.Gly930Val) c.900-4158G>T n.692G>T n.617G>T c.2948G>T (p.Gly983Val) c.*28+28261G>T (n.*28+28261G>T) c.2813G>T (p.Gly938Val) c.2147G>T (p.Gly716Val) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201190G>A | CA454968500 | EGFR | c.2790G>A (p.Gly930=) c.900-4157G>A n.693G>A n.618G>A c.2949G>A (p.Gly983=) c.*28+28262G>A (n.*28+28262G>A) c.2814G>A (p.Gly938=) c.2148G>A (p.Gly716=) | dbSNP |
| 7 | g.55201190G>C | CA454968501 | EGFR | c.2790G>C (p.Gly930=) c.900-4157G>C n.693G>C n.618G>C c.2949G>C (p.Gly983=) c.*28+28262G>C (n.*28+28262G>C) c.2814G>C (p.Gly938=) c.2148G>C (p.Gly716=) | dbSNP |
| 7 | g.55201190G>T | CA454968502 | EGFR | c.2790G>T (p.Gly930=) c.900-4157G>T n.693G>T n.618G>T c.2949G>T (p.Gly983=) c.*28+28262G>T (n.*28+28262G>T) c.2814G>T (p.Gly938=) c.2148G>T (p.Gly716=) | |
| 7 | g.55201191G>A | CA158937824 | EGFR | c.2791G>A (p.Asp931Asn) c.900-4156G>A n.694G>A n.619G>A c.2950G>A (p.Asp984Asn) c.*28+28263G>A (n.*28+28263G>A) c.2815G>A (p.Asp939Asn) c.2149G>A (p.Asp717Asn) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55201191G>C | CA367582337 | EGFR | c.2791G>C (p.Asp931His) c.900-4156G>C n.694G>C n.619G>C c.2950G>C (p.Asp984His) c.*28+28263G>C (n.*28+28263G>C) c.2815G>C (p.Asp939His) c.2149G>C (p.Asp717His) | dbSNP |
| 7 | g.55201191G= | CA1708928409 | EGFR | c.2791G= (p.Asp931=) c.900-4156G= n.694G= n.619G= c.2950G= (p.Asp984=) c.*28+28263G= (n.*28+28263G=) c.2815G= (p.Asp939=) c.2149G= (p.Asp717=) | |
| 7 | g.55201191G>T | CA367582338 | EGFR | c.2791G>T (p.Asp931Tyr) c.900-4156G>T n.694G>T n.619G>T c.2950G>T (p.Asp984Tyr) c.*28+28263G>T (n.*28+28263G>T) c.2815G>T (p.Asp939Tyr) c.2149G>T (p.Asp717Tyr) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201192A>C | CA367582339 | EGFR | c.2792A>C (p.Asp931Ala) c.900-4155A>C n.695A>C n.620A>C c.2951A>C (p.Asp984Ala) c.*28+28264A>C (n.*28+28264A>C) c.2816A>C (p.Asp939Ala) c.2150A>C (p.Asp717Ala) | |
| 7 | g.55201192A>G | CA367582341 | EGFR | c.2792A>G (p.Asp931Gly) c.900-4155A>G n.695A>G n.620A>G c.2951A>G (p.Asp984Gly) c.*28+28264A>G (n.*28+28264A>G) c.2816A>G (p.Asp939Gly) c.2150A>G (p.Asp717Gly) | dbSNP gnomAD v4 |
| 7 | g.55201192A>T | CA367582340 | EGFR | c.2792A>T (p.Asp931Val) c.900-4155A>T n.695A>T n.620A>T c.2951A>T (p.Asp984Val) c.*28+28264A>T (n.*28+28264A>T) c.2816A>T (p.Asp939Val) c.2150A>T (p.Asp717Val) | dbSNP |
| 7 | g.55201193T>A | CA367582342 | EGFR | c.2793T>A (p.Asp931Glu) c.900-4154T>A n.696T>A n.621T>A c.2952T>A (p.Asp984Glu) c.*28+28265T>A (n.*28+28265T>A) c.2817T>A (p.Asp939Glu) c.2151T>A (p.Asp717Glu) | dbSNP |
| 7 | g.55201193T>C | CA454968503 | EGFR | c.2793T>C (p.Asp931=) c.900-4154T>C n.696T>C n.621T>C c.2952T>C (p.Asp984=) c.*28+28265T>C (n.*28+28265T>C) c.2817T>C (p.Asp939=) c.2151T>C (p.Asp717=) | |
| 7 | g.55201193T>G | CA367582343 | EGFR | c.2793T>G (p.Asp931Glu) c.900-4154T>G n.696T>G n.621T>G c.2952T>G (p.Asp984Glu) c.*28+28265T>G (n.*28+28265T>G) c.2817T>G (p.Asp939Glu) c.2151T>G (p.Asp717Glu) | dbSNP |
| 7 | g.55201194G>A | CA367582344 | EGFR | c.2794G>A (p.Glu932Lys) c.900-4153G>A n.697G>A n.622G>A c.2953G>A (p.Glu985Lys) c.*28+28266G>A (n.*28+28266G>A) c.2818G>A (p.Glu940Lys) c.2152G>A (p.Glu718Lys) | |
| 7 | g.55201194G>C | CA367582345 | EGFR | c.2794G>C (p.Glu932Gln) c.900-4153G>C n.697G>C n.622G>C c.2953G>C (p.Glu985Gln) c.*28+28266G>C (n.*28+28266G>C) c.2818G>C (p.Glu940Gln) c.2152G>C (p.Glu718Gln) | dbSNP |
| 7 | g.55201194G>T | CA367582346 | EGFR | c.2794G>T (p.Glu932Ter) c.900-4153G>T n.697G>T n.622G>T c.2953G>T (p.Glu985Ter) c.*28+28266G>T (n.*28+28266G>T) c.2818G>T (p.Glu940Ter) c.2152G>T (p.Glu718Ter) | |
| 7 | g.55201197_55201200del | CA2697557285 | EGFR | c.2797_2800del (p.Arg933CysfsTer15) c.900-4150_900-4147del n.700_703del n.625_628del c.2956_2959del (p.Arg986CysfsTer15) c.*28+28269_*28+28272del (n.*28+28269_*28+28272del) c.2821_2824del (p.Arg941CysfsTer15) c.2155_2158del (p.Arg719CysfsTer15) | ClinVar |
| 7 | g.55201195A>C | CA367582347 | EGFR | c.2795A>C (p.Glu932Ala) c.900-4152A>C n.698A>C n.623A>C c.2954A>C (p.Glu985Ala) c.*28+28267A>C (n.*28+28267A>C) c.2819A>C (p.Glu940Ala) c.2153A>C (p.Glu718Ala) | |
| 7 | g.55201195A>G | CA367582348 | EGFR | c.2795A>G (p.Glu932Gly) c.900-4152A>G n.698A>G n.623A>G c.2954A>G (p.Glu985Gly) c.*28+28267A>G (n.*28+28267A>G) c.2819A>G (p.Glu940Gly) c.2153A>G (p.Glu718Gly) | ClinVar dbSNP |
| 7 | g.55201195A>T | CA367582349 | EGFR | c.2795A>T (p.Glu932Val) c.900-4152A>T n.698A>T n.623A>T c.2954A>T (p.Glu985Val) c.*28+28267A>T (n.*28+28267A>T) c.2819A>T (p.Glu940Val) c.2153A>T (p.Glu718Val) | dbSNP |
| 7 | g.55201196A>C | CA367582350 | EGFR | c.2796A>C (p.Glu932Asp) c.900-4151A>C n.699A>C n.624A>C c.2955A>C (p.Glu985Asp) c.*28+28268A>C (n.*28+28268A>C) c.2820A>C (p.Glu940Asp) c.2154A>C (p.Glu718Asp) | |
| 7 | g.55201196A>G | CA454968505 | EGFR | c.2796A>G (p.Glu932=) c.900-4151A>G n.699A>G n.624A>G c.2955A>G (p.Glu985=) c.*28+28268A>G (n.*28+28268A>G) c.2820A>G (p.Glu940=) c.2154A>G (p.Glu718=) | |
| 7 | g.55201196A>T | CA367582351 | EGFR | c.2796A>T (p.Glu932Asp) c.900-4151A>T n.699A>T n.624A>T c.2955A>T (p.Glu985Asp) c.*28+28268A>T (n.*28+28268A>T) c.2820A>T (p.Glu940Asp) c.2154A>T (p.Glu718Asp) | |
| 7 | g.55201197A>C | CA454968506 | EGFR | c.2797A>C (p.Arg933=) c.900-4150A>C n.700A>C n.625A>C c.2956A>C (p.Arg986=) c.*28+28269A>C (n.*28+28269A>C) c.2821A>C (p.Arg941=) c.2155A>C (p.Arg719=) | |
| 7 | g.55201197A>G | CA367582353 | EGFR | c.2797A>G (p.Arg933Gly) c.900-4150A>G n.700A>G n.625A>G c.2956A>G (p.Arg986Gly) c.*28+28269A>G (n.*28+28269A>G) c.2821A>G (p.Arg941Gly) c.2155A>G (p.Arg719Gly) | |
| 7 | g.55201197A>T | CA367582352 | EGFR | c.2797A>T (p.Arg933Ter) c.900-4150A>T n.700A>T n.625A>T c.2956A>T (p.Arg986Ter) c.*28+28269A>T (n.*28+28269A>T) c.2821A>T (p.Arg941Ter) c.2155A>T (p.Arg719Ter) | dbSNP |
| 7 | g.55201198G>A | CA4266227 | EGFR | c.2798G>A (p.Arg933Lys) c.900-4149G>A n.701G>A n.626G>A c.2957G>A (p.Arg986Lys) c.*28+28270G>A (n.*28+28270G>A) c.2822G>A (p.Arg941Lys) c.2156G>A (p.Arg719Lys) | dbSNP ExAC |
| 7 | g.55201198G>C | CA367582354 | EGFR | c.2798G>C (p.Arg933Thr) c.900-4149G>C n.701G>C n.626G>C c.2957G>C (p.Arg986Thr) c.*28+28270G>C (n.*28+28270G>C) c.2822G>C (p.Arg941Thr) c.2156G>C (p.Arg719Thr) | dbSNP |
| 7 | g.55201198G= | CA1708928410 | EGFR | c.2798G= (p.Arg933=) c.900-4149G= n.701G= n.626G= c.2957G= (p.Arg986=) c.*28+28270G= (n.*28+28270G=) c.2822G= (p.Arg941=) c.2156G= (p.Arg719=) | |
| 7 | g.55201198G>T | CA367582355 | EGFR | c.2798G>T (p.Arg933Ile) c.900-4149G>T n.701G>T n.626G>T c.2957G>T (p.Arg986Ile) c.*28+28270G>T (n.*28+28270G>T) c.2822G>T (p.Arg941Ile) c.2156G>T (p.Arg719Ile) | gnomAD v4 |
| 7 | g.55201199A>C | CA367582356 | EGFR | c.2799A>C (p.Arg933Ser) c.900-4148A>C n.702A>C n.627A>C c.2958A>C (p.Arg986Ser) c.*28+28271A>C (n.*28+28271A>C) c.2823A>C (p.Arg941Ser) c.2157A>C (p.Arg719Ser) | |
| 7 | g.55201199A>G | CA454968508 | EGFR | c.2799A>G (p.Arg933=) c.900-4148A>G n.702A>G n.627A>G c.2958A>G (p.Arg986=) c.*28+28271A>G (n.*28+28271A>G) c.2823A>G (p.Arg941=) c.2157A>G (p.Arg719=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201199A>T | CA367582357 | EGFR | c.2799A>T (p.Arg933Ser) c.900-4148A>T n.702A>T n.627A>T c.2958A>T (p.Arg986Ser) c.*28+28271A>T (n.*28+28271A>T) c.2823A>T (p.Arg941Ser) c.2157A>T (p.Arg719Ser) | dbSNP |
| 7 | g.55201200A>C | CA367582360 | EGFR | c.2800A>C (p.Met934Leu) c.900-4147A>C n.703A>C n.628A>C c.2959A>C (p.Met987Leu) c.*28+28272A>C (n.*28+28272A>C) c.2824A>C (p.Met942Leu) c.2158A>C (p.Met720Leu) | |
| 7 | g.55201200A>G | CA367582359 | EGFR | c.2800A>G (p.Met934Val) c.900-4147A>G n.703A>G n.628A>G c.2959A>G (p.Met987Val) c.*28+28272A>G (n.*28+28272A>G) c.2824A>G (p.Met942Val) c.2158A>G (p.Met720Val) | ClinVar |
| 7 | g.55201200A>T | CA367582358 | EGFR | c.2800A>T (p.Met934Leu) c.900-4147A>T n.703A>T n.628A>T c.2959A>T (p.Met987Leu) c.*28+28272A>T (n.*28+28272A>T) c.2824A>T (p.Met942Leu) c.2158A>T (p.Met720Leu) | dbSNP |
| 7 | g.55201201T>A | CA367582361 | EGFR | c.2801T>A (p.Met934Lys) c.900-4146T>A n.704T>A n.629T>A c.2960T>A (p.Met987Lys) c.*28+28273T>A (n.*28+28273T>A) c.2825T>A (p.Met942Lys) c.2159T>A (p.Met720Lys) | dbSNP |
| 7 | g.55201201T>C | CA367582362 | EGFR | c.2801T>C (p.Met934Thr) c.900-4146T>C n.704T>C n.629T>C c.2960T>C (p.Met987Thr) c.*28+28273T>C (n.*28+28273T>C) c.2825T>C (p.Met942Thr) c.2159T>C (p.Met720Thr) | dbSNP |
| 7 | g.55201201T>G | CA367582363 | EGFR | c.2801T>G (p.Met934Arg) c.900-4146T>G n.704T>G n.629T>G c.2960T>G (p.Met987Arg) c.*28+28273T>G (n.*28+28273T>G) c.2825T>G (p.Met942Arg) c.2159T>G (p.Met720Arg) | dbSNP COSMIC |
| 7 | g.55201202G>A | CA367582364 | EGFR | c.2802G>A (p.Met934Ile) c.900-4145G>A n.705G>A n.630G>A c.2961G>A (p.Met987Ile) c.*28+28274G>A (n.*28+28274G>A) c.2826G>A (p.Met942Ile) c.2160G>A (p.Met720Ile) | dbSNP gnomAD v4 |
| 7 | g.55201202G>C | CA367582365 | EGFR | c.2802G>C (p.Met934Ile) c.900-4145G>C n.705G>C n.630G>C c.2961G>C (p.Met987Ile) c.*28+28274G>C (n.*28+28274G>C) c.2826G>C (p.Met942Ile) c.2160G>C (p.Met720Ile) | dbSNP |
| 7 | g.55201202G>T | CA367582366 | EGFR | c.2802G>T (p.Met934Ile) c.900-4145G>T n.705G>T n.630G>T c.2961G>T (p.Met987Ile) c.*28+28274G>T (n.*28+28274G>T) c.2826G>T (p.Met942Ile) c.2160G>T (p.Met720Ile) | dbSNP |
| 7 | g.55201203C>A | CA367582367 | EGFR | c.2803C>A (p.His935Asn) c.900-4144C>A n.706C>A n.631C>A c.2962C>A (p.His988Asn) c.*28+28275C>A (n.*28+28275C>A) c.2827C>A (p.His943Asn) c.2161C>A (p.His721Asn) | ClinVar dbSNP |
| 7 | g.55201203C= | CA1708928411 | EGFR | c.2803C= (p.His935=) c.900-4144C= n.706C= n.631C= c.2962C= (p.His988=) c.*28+28275C= (n.*28+28275C=) c.2827C= (p.His943=) c.2161C= (p.His721=) | |
| 7 | g.55201203C>G | CA367582369 | EGFR | c.2803C>G (p.His935Asp) c.900-4144C>G n.706C>G n.631C>G c.2962C>G (p.His988Asp) c.*28+28275C>G (n.*28+28275C>G) c.2827C>G (p.His943Asp) c.2161C>G (p.His721Asp) | dbSNP |
| 7 | g.55201203C>T | CA367582368 | EGFR | c.2803C>T (p.His935Tyr) c.900-4144C>T n.706C>T n.631C>T c.2962C>T (p.His988Tyr) c.*28+28275C>T (n.*28+28275C>T) c.2827C>T (p.His943Tyr) c.2161C>T (p.His721Tyr) | dbSNP gnomAD v4 |
| 7 | g.55201204A= | CA1708928412 | EGFR | c.2804A= (p.His935=) c.900-4143A= n.707A= n.632A= c.2963A= (p.His988=) c.*28+28276A= (n.*28+28276A=) c.2828A= (p.His943=) c.2162A= (p.His721=) | |
| 7 | g.55201204A>C | CA158465 | EGFR | c.2804A>C (p.His935Pro) c.900-4143A>C n.707A>C n.632A>C c.2963A>C (p.His988Pro) c.*28+28276A>C (n.*28+28276A>C) c.2828A>C (p.His943Pro) c.2162A>C (p.His721Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201204A>G | CA4266228 | EGFR | c.2804A>G (p.His935Arg) c.900-4143A>G n.707A>G n.632A>G c.2963A>G (p.His988Arg) c.*28+28276A>G (n.*28+28276A>G) c.2828A>G (p.His943Arg) c.2162A>G (p.His721Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201204A>T | CA367582370 | EGFR | c.2804A>T (p.His935Leu) c.900-4143A>T n.707A>T n.632A>T c.2963A>T (p.His988Leu) c.*28+28276A>T (n.*28+28276A>T) c.2828A>T (p.His943Leu) c.2162A>T (p.His721Leu) | |
| 7 | g.55201205T>A | CA367582371 | EGFR | c.2805T>A (p.His935Gln) c.900-4142T>A n.708T>A n.633T>A c.2964T>A (p.His988Gln) c.*28+28277T>A (n.*28+28277T>A) c.2829T>A (p.His943Gln) c.2163T>A (p.His721Gln) | dbSNP |
| 7 | g.55201205T>C | CA454968509 | EGFR | c.2805T>C (p.His935=) c.900-4142T>C n.708T>C n.633T>C c.2964T>C (p.His988=) c.*28+28277T>C (n.*28+28277T>C) c.2829T>C (p.His943=) c.2163T>C (p.His721=) | dbSNP |
| 7 | g.55201205T>G | CA367582372 | EGFR | c.2805T>G (p.His935Gln) c.900-4142T>G n.708T>G n.633T>G c.2964T>G (p.His988Gln) c.*28+28277T>G (n.*28+28277T>G) c.2829T>G (p.His943Gln) c.2163T>G (p.His721Gln) | |
| 7 | g.55201206T>A | CA367582373 | EGFR | c.2806T>A (p.Leu936Met) c.900-4141T>A n.709T>A n.634T>A c.2965T>A (p.Leu989Met) c.*28+28278T>A (n.*28+28278T>A) c.2830T>A (p.Leu944Met) c.2164T>A (p.Leu722Met) | dbSNP |
| 7 | g.55201206T>C | CA454968510 | EGFR | c.2806T>C (p.Leu936=) c.900-4141T>C n.709T>C n.634T>C c.2965T>C (p.Leu989=) c.*28+28278T>C (n.*28+28278T>C) c.2830T>C (p.Leu944=) c.2164T>C (p.Leu722=) | dbSNP |
| 7 | g.55201206T>G | CA367582374 | EGFR | c.2806T>G (p.Leu936Val) c.900-4141T>G n.709T>G n.634T>G c.2965T>G (p.Leu989Val) c.*28+28278T>G (n.*28+28278T>G) c.2830T>G (p.Leu944Val) c.2164T>G (p.Leu722Val) | |
| 7 | g.55201207T>A | CA367582375 | EGFR | c.2807T>A (p.Leu936Ter) c.900-4140T>A n.710T>A n.635T>A c.2966T>A (p.Leu989Ter) c.*28+28279T>A (n.*28+28279T>A) c.2831T>A (p.Leu944Ter) c.2165T>A (p.Leu722Ter) | dbSNP |
| 7 | g.55201207T>C | CA367582376 | EGFR | c.2807T>C (p.Leu936Ser) c.900-4140T>C n.710T>C n.635T>C c.2966T>C (p.Leu989Ser) c.*28+28279T>C (n.*28+28279T>C) c.2831T>C (p.Leu944Ser) c.2165T>C (p.Leu722Ser) | |
| 7 | g.55201207T>G | CA367582377 | EGFR | c.2807T>G (p.Leu936Trp) c.900-4140T>G n.710T>G n.635T>G c.2966T>G (p.Leu989Trp) c.*28+28279T>G (n.*28+28279T>G) c.2831T>G (p.Leu944Trp) c.2165T>G (p.Leu722Trp) | |
| 7 | g.55201208G>A | CA454968511 | EGFR | c.2808G>A (p.Leu936=) c.900-4139G>A n.711G>A n.636G>A c.2967G>A (p.Leu989=) c.*28+28280G>A (n.*28+28280G>A) c.2832G>A (p.Leu944=) c.2166G>A (p.Leu722=) | dbSNP |
| 7 | g.55201208G>C | CA367582378 | EGFR | c.2808G>C (p.Leu936Phe) c.900-4139G>C n.711G>C n.636G>C c.2967G>C (p.Leu989Phe) c.*28+28280G>C (n.*28+28280G>C) c.2832G>C (p.Leu944Phe) c.2166G>C (p.Leu722Phe) | dbSNP |
| 7 | g.55201208G>T | CA367582379 | EGFR | c.2808G>T (p.Leu936Phe) c.900-4139G>T n.711G>T n.636G>T c.2967G>T (p.Leu989Phe) c.*28+28280G>T (n.*28+28280G>T) c.2832G>T (p.Leu944Phe) c.2166G>T (p.Leu722Phe) | dbSNP |
| 7 | g.55201209C>A | CA367582380 | EGFR | c.2809C>A (p.Pro937Thr) c.900-4138C>A n.712C>A n.637C>A c.2968C>A (p.Pro990Thr) c.*28+28281C>A (n.*28+28281C>A) c.2833C>A (p.Pro945Thr) c.2167C>A (p.Pro723Thr) | dbSNP |
| 7 | g.55201209C= | CA1708928413 | EGFR | c.2809C= (p.Pro937=) c.900-4138C= n.712C= n.637C= c.2968C= (p.Pro990=) c.*28+28281C= (n.*28+28281C=) c.2833C= (p.Pro945=) c.2167C= (p.Pro723=) | |
| 7 | g.55201209C>G | CA367582381 | EGFR | c.2809C>G (p.Pro937Ala) c.900-4138C>G n.712C>G n.637C>G c.2968C>G (p.Pro990Ala) c.*28+28281C>G (n.*28+28281C>G) c.2833C>G (p.Pro945Ala) c.2167C>G (p.Pro723Ala) | dbSNP |
| 7 | g.55201209C>T | CA4266229 | EGFR | c.2809C>T (p.Pro937Ser) c.900-4138C>T n.712C>T n.637C>T c.2968C>T (p.Pro990Ser) c.*28+28281C>T (n.*28+28281C>T) c.2833C>T (p.Pro945Ser) c.2167C>T (p.Pro723Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201210C>A | CA367582383 | EGFR | c.2810C>A (p.Pro937Gln) c.900-4137C>A n.713C>A n.638C>A c.2969C>A (p.Pro990Gln) c.*28+28282C>A (n.*28+28282C>A) c.2834C>A (p.Pro945Gln) c.2168C>A (p.Pro723Gln) | dbSNP |
| 7 | g.55201210C>G | CA367582382 | EGFR | c.2810C>G (p.Pro937Arg) c.900-4137C>G n.713C>G n.638C>G c.2969C>G (p.Pro990Arg) c.*28+28282C>G (n.*28+28282C>G) c.2834C>G (p.Pro945Arg) c.2168C>G (p.Pro723Arg) | dbSNP gnomAD v4 |
| 7 | g.55201210C>T | CA367582384 | EGFR | c.2810C>T (p.Pro937Leu) c.900-4137C>T n.713C>T n.638C>T c.2969C>T (p.Pro990Leu) c.*28+28282C>T (n.*28+28282C>T) c.2834C>T (p.Pro945Leu) c.2168C>T (p.Pro723Leu) | dbSNP |
| 7 | g.55201211A>C | CA454968515 | EGFR | c.2811A>C (p.Pro937=) c.900-4136A>C n.714A>C n.639A>C c.2970A>C (p.Pro990=) c.*28+28283A>C (n.*28+28283A>C) c.2835A>C (p.Pro945=) c.2169A>C (p.Pro723=) | |
| 7 | g.55201211A>G | CA454968516 | EGFR | c.2811A>G (p.Pro937=) c.900-4136A>G n.714A>G n.639A>G c.2970A>G (p.Pro990=) c.*28+28283A>G (n.*28+28283A>G) c.2835A>G (p.Pro945=) c.2169A>G (p.Pro723=) | dbSNP |
| 7 | g.55201211A>T | CA454968517 | EGFR | c.2811A>T (p.Pro937=) c.900-4136A>T n.714A>T n.639A>T c.2970A>T (p.Pro990=) c.*28+28283A>T (n.*28+28283A>T) c.2835A>T (p.Pro945=) c.2169A>T (p.Pro723=) | dbSNP |
| 7 | g.55201212A= | CA1708928414 | EGFR | c.2812A= (p.Ser938=) c.900-4135A= n.715A= n.640A= c.2971A= (p.Ser991=) c.*28+28284A= (n.*28+28284A=) c.2836A= (p.Ser946=) c.2170A= (p.Ser724=) | |
| 7 | g.55201212A>C | CA4266231 | EGFR | c.2812A>C (p.Ser938Arg) c.900-4135A>C n.715A>C n.640A>C c.2971A>C (p.Ser991Arg) c.*28+28284A>C (n.*28+28284A>C) c.2836A>C (p.Ser946Arg) c.2170A>C (p.Ser724Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201212A>G | CA4266230 | EGFR | c.2812A>G (p.Ser938Gly) c.900-4135A>G n.715A>G n.640A>G c.2971A>G (p.Ser991Gly) c.*28+28284A>G (n.*28+28284A>G) c.2836A>G (p.Ser946Gly) c.2170A>G (p.Ser724Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201212A>T | CA367582385 | EGFR | c.2812A>T (p.Ser938Cys) c.900-4135A>T n.715A>T n.640A>T c.2971A>T (p.Ser991Cys) c.*28+28284A>T (n.*28+28284A>T) c.2836A>T (p.Ser946Cys) c.2170A>T (p.Ser724Cys) | |
| 7 | g.55201213G>A | CA367582386 | EGFR | c.2813G>A (p.Ser938Asn) c.900-4134G>A n.716G>A n.641G>A c.2972G>A (p.Ser991Asn) c.*28+28285G>A (n.*28+28285G>A) c.2837G>A (p.Ser946Asn) c.2171G>A (p.Ser724Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201213G>C | CA367582387 | EGFR | c.2813G>C (p.Ser938Thr) c.900-4134G>C n.716G>C n.641G>C c.2972G>C (p.Ser991Thr) c.*28+28285G>C (n.*28+28285G>C) c.2837G>C (p.Ser946Thr) c.2171G>C (p.Ser724Thr) | ClinVar dbSNP |
| 7 | g.55201213G= | CA1708928415 | EGFR | c.2813G= (p.Ser938=) c.900-4134G= n.716G= n.641G= c.2972G= (p.Ser991=) c.*28+28285G= (n.*28+28285G=) c.2837G= (p.Ser946=) c.2171G= (p.Ser724=) | |
| 7 | g.55201213G>T | CA367582388 | EGFR | c.2813G>T (p.Ser938Ile) c.900-4134G>T n.716G>T n.641G>T c.2972G>T (p.Ser991Ile) c.*28+28285G>T (n.*28+28285G>T) c.2837G>T (p.Ser946Ile) c.2171G>T (p.Ser724Ile) | |
| 7 | g.55201214T>A | CA367582390 | EGFR | c.2814T>A (p.Ser938Arg) c.900-4133T>A n.717T>A n.642T>A c.2973T>A (p.Ser991Arg) c.*28+28286T>A (n.*28+28286T>A) c.2838T>A (p.Ser946Arg) c.2172T>A (p.Ser724Arg) | dbSNP |
| 7 | g.55201214T>C | CA454968520 | EGFR | c.2814T>C (p.Ser938=) c.900-4133T>C n.717T>C n.642T>C c.2973T>C (p.Ser991=) c.*28+28286T>C (n.*28+28286T>C) c.2838T>C (p.Ser946=) c.2172T>C (p.Ser724=) | dbSNP |
| 7 | g.55201214T>G | CA367582389 | EGFR | c.2814T>G (p.Ser938Arg) c.900-4133T>G n.717T>G n.642T>G c.2973T>G (p.Ser991Arg) c.*28+28286T>G (n.*28+28286T>G) c.2838T>G (p.Ser946Arg) c.2172T>G (p.Ser724Arg) | dbSNP |
| 7 | g.55201215C>A | CA367582391 | EGFR | c.2815C>A (p.Pro939Thr) c.900-4132C>A n.718C>A n.643C>A c.2974C>A (p.Pro992Thr) c.*28+28287C>A (n.*28+28287C>A) c.2839C>A (p.Pro947Thr) c.2173C>A (p.Pro725Thr) | dbSNP |
| 7 | g.55201215C>G | CA367582392 | EGFR | c.2815C>G (p.Pro939Ala) c.900-4132C>G n.718C>G n.643C>G c.2974C>G (p.Pro992Ala) c.*28+28287C>G (n.*28+28287C>G) c.2839C>G (p.Pro947Ala) c.2173C>G (p.Pro725Ala) | dbSNP |
| 7 | g.55201215C>T | CA367582393 | EGFR | c.2815C>T (p.Pro939Ser) c.900-4132C>T n.718C>T n.643C>T c.2974C>T (p.Pro992Ser) c.*28+28287C>T (n.*28+28287C>T) c.2839C>T (p.Pro947Ser) c.2173C>T (p.Pro725Ser) | dbSNP |
| 7 | g.55201216C>A | CA367582394 | EGFR | c.2816C>A (p.Pro939His) c.900-4131C>A n.719C>A n.644C>A c.2975C>A (p.Pro992His) c.*28+28288C>A (n.*28+28288C>A) c.2840C>A (p.Pro947His) c.2174C>A (p.Pro725His) | dbSNP |
| 7 | g.55201216C>G | CA367582395 | EGFR | c.2816C>G (p.Pro939Arg) c.900-4131C>G n.719C>G n.644C>G c.2975C>G (p.Pro992Arg) c.*28+28288C>G (n.*28+28288C>G) c.2840C>G (p.Pro947Arg) c.2174C>G (p.Pro725Arg) | dbSNP |
| 7 | g.55201216C>T | CA367582396 | EGFR | c.2816C>T (p.Pro939Leu) c.900-4131C>T n.719C>T n.644C>T c.2975C>T (p.Pro992Leu) c.*28+28288C>T (n.*28+28288C>T) c.2840C>T (p.Pro947Leu) c.2174C>T (p.Pro725Leu) | dbSNP |
| 7 | g.55201217T>A | CA454968523 | EGFR | c.2817T>A (p.Pro939=) c.900-4130T>A n.720T>A n.645T>A c.2976T>A (p.Pro992=) c.*28+28289T>A (n.*28+28289T>A) c.2841T>A (p.Pro947=) c.2175T>A (p.Pro725=) | |
| 7 | g.55201217T>C | CA454968524 | EGFR | c.2817T>C (p.Pro939=) c.900-4130T>C n.720T>C n.645T>C c.2976T>C (p.Pro992=) c.*28+28289T>C (n.*28+28289T>C) c.2841T>C (p.Pro947=) c.2175T>C (p.Pro725=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201217T>G | CA454968522 | EGFR | c.2817T>G (p.Pro939=) c.900-4130T>G n.720T>G n.645T>G c.2976T>G (p.Pro992=) c.*28+28289T>G (n.*28+28289T>G) c.2841T>G (p.Pro947=) c.2175T>G (p.Pro725=) | ClinVar |
| 7 | g.55201217T= | CA1708928416 | EGFR | c.2817T= (p.Pro939=) c.900-4130T= n.720T= n.645T= c.2976T= (p.Pro992=) c.*28+28289T= (n.*28+28289T=) c.2841T= (p.Pro947=) c.2175T= (p.Pro725=) | |
| 7 | g.55201218A>C | CA367582397 | EGFR | c.2818A>C (p.Thr940Pro) c.900-4129A>C n.721A>C n.646A>C c.2977A>C (p.Thr993Pro) c.*28+28290A>C (n.*28+28290A>C) c.2842A>C (p.Thr948Pro) c.2176A>C (p.Thr726Pro) | ClinVar dbSNP |
| 7 | g.55201218A>G | CA367582399 | EGFR | c.2818A>G (p.Thr940Ala) c.900-4129A>G n.721A>G n.646A>G c.2977A>G (p.Thr993Ala) c.*28+28290A>G (n.*28+28290A>G) c.2842A>G (p.Thr948Ala) c.2176A>G (p.Thr726Ala) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201218A>T | CA367582398 | EGFR | c.2818A>T (p.Thr940Ser) c.900-4129A>T n.721A>T n.646A>T c.2977A>T (p.Thr993Ser) c.*28+28290A>T (n.*28+28290A>T) c.2842A>T (p.Thr948Ser) c.2176A>T (p.Thr726Ser) | dbSNP |
| 7 | g.55201219C>A | CA367582400 | EGFR | c.2819C>A (p.Thr940Lys) c.900-4128C>A n.722C>A n.647C>A c.2978C>A (p.Thr993Lys) c.*28+28291C>A (n.*28+28291C>A) c.2843C>A (p.Thr948Lys) c.2177C>A (p.Thr726Lys) | dbSNP |
| 7 | g.55201219C>G | CA367582401 | EGFR | c.2819C>G (p.Thr940Arg) c.900-4128C>G n.722C>G n.647C>G c.2978C>G (p.Thr993Arg) c.*28+28291C>G (n.*28+28291C>G) c.2843C>G (p.Thr948Arg) c.2177C>G (p.Thr726Arg) | dbSNP |
| 7 | g.55201219C>T | CA367582402 | EGFR | c.2819C>T (p.Thr940Ile) c.900-4128C>T n.722C>T n.647C>T c.2978C>T (p.Thr993Ile) c.*28+28291C>T (n.*28+28291C>T) c.2843C>T (p.Thr948Ile) c.2177C>T (p.Thr726Ile) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201220A>C | CA454968527 | EGFR | c.2820A>C (p.Thr940=) c.900-4127A>C n.723A>C n.648A>C c.2979A>C (p.Thr993=) c.*28+28292A>C (n.*28+28292A>C) c.2844A>C (p.Thr948=) c.2178A>C (p.Thr726=) | |
| 7 | g.55201220A>G | CA454968528 | EGFR | c.2820A>G (p.Thr940=) c.900-4127A>G n.723A>G n.648A>G c.2979A>G (p.Thr993=) c.*28+28292A>G (n.*28+28292A>G) c.2844A>G (p.Thr948=) c.2178A>G (p.Thr726=) | |
| 7 | g.55201220A>T | CA454968529 | EGFR | c.2820A>T (p.Thr940=) c.900-4127A>T n.723A>T n.648A>T c.2979A>T (p.Thr993=) c.*28+28292A>T (n.*28+28292A>T) c.2844A>T (p.Thr948=) c.2178A>T (p.Thr726=) | dbSNP |
| 7 | g.55201221G>A | CA367582403 | EGFR | c.2821G>A (p.Asp941Asn) c.900-4126G>A n.724G>A n.649G>A c.2980G>A (p.Asp994Asn) c.*28+28293G>A (n.*28+28293G>A) c.2845G>A (p.Asp949Asn) c.2179G>A (p.Asp727Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201221G>C | CA367582404 | EGFR | c.2821G>C (p.Asp941His) c.900-4126G>C n.724G>C n.649G>C c.2980G>C (p.Asp994His) c.*28+28293G>C (n.*28+28293G>C) c.2845G>C (p.Asp949His) c.2179G>C (p.Asp727His) | |
| 7 | g.55201221G= | CA1708928417 | EGFR | c.2821G= (p.Asp941=) c.900-4126G= n.724G= n.649G= c.2980G= (p.Asp994=) c.*28+28293G= (n.*28+28293G=) c.2845G= (p.Asp949=) c.2179G= (p.Asp727=) | |
| 7 | g.55201221G>T | CA367582405 | EGFR | c.2821G>T (p.Asp941Tyr) c.900-4126G>T n.724G>T n.649G>T c.2980G>T (p.Asp994Tyr) c.*28+28293G>T (n.*28+28293G>T) c.2845G>T (p.Asp949Tyr) c.2179G>T (p.Asp727Tyr) | |
| 7 | g.55201222A>C | CA367582406 | EGFR | c.2822A>C (p.Asp941Ala) c.900-4125A>C n.725A>C n.650A>C c.2981A>C (p.Asp994Ala) c.*28+28294A>C (n.*28+28294A>C) c.2846A>C (p.Asp949Ala) c.2180A>C (p.Asp727Ala) | ClinVar dbSNP |
| 7 | g.55201222A>G | CA367582407 | EGFR | c.2822A>G (p.Asp941Gly) c.900-4125A>G n.725A>G n.650A>G c.2981A>G (p.Asp994Gly) c.*28+28294A>G (n.*28+28294A>G) c.2846A>G (p.Asp949Gly) c.2180A>G (p.Asp727Gly) | dbSNP |
| 7 | g.55201222A>T | CA367582408 | EGFR | c.2822A>T (p.Asp941Val) c.900-4125A>T n.725A>T n.650A>T c.2981A>T (p.Asp994Val) c.*28+28294A>T (n.*28+28294A>T) c.2846A>T (p.Asp949Val) c.2180A>T (p.Asp727Val) | dbSNP |
| 7 | g.55201222_55201224delinsACT | CA1708928418 | EGFR | c.2822_2824delinsACT (p.Asp941=) c.900-4125_900-4123delinsACT n.725_727delinsACT n.650_652delinsACT c.2981_2983delinsACT (p.Asp994=) c.*28+28294_*28+28296delinsACT (n.*28+28294_*28+28296delinsACT) c.2846_2848delinsACT (p.Asp949=) c.2180_2182delinsACT (p.Asp727=) | |
| 7 | g.55201222_55201224delinsGTG | CA158462 | EGFR | c.2822_2824delinsGTG (p.Asp941_Ser942delinsGlyAla) c.900-4125_900-4123delinsGTG n.725_727delinsGTG n.650_652delinsGTG c.2981_2983delinsGTG (p.Asp994_Ser995delinsGlyAla) c.*28+28294_*28+28296delinsGTG (n.*28+28294_*28+28296delinsGTG) c.2846_2848delinsGTG (p.Asp949_Ser950delinsGlyAla) c.2180_2182delinsGTG (p.Asp727_Ser728delinsGlyAla) | ClinVar dbSNP |
| 7 | g.55201223C>A | CA367582410 | EGFR | c.2823C>A (p.Asp941Glu) c.900-4124C>A n.726C>A n.651C>A c.2982C>A (p.Asp994Glu) c.*28+28295C>A (n.*28+28295C>A) c.2847C>A (p.Asp949Glu) c.2181C>A (p.Asp727Glu) | |
| 7 | g.55201223C= | CA1708928419 | EGFR | c.2823C= (p.Asp941=) c.900-4124C= n.726C= n.651C= c.2982C= (p.Asp994=) c.*28+28295C= (n.*28+28295C=) c.2847C= (p.Asp949=) c.2181C= (p.Asp727=) | |
| 7 | g.55201223C>G | CA367582409 | EGFR | c.2823C>G (p.Asp941Glu) c.900-4124C>G n.726C>G n.651C>G c.2982C>G (p.Asp994Glu) c.*28+28295C>G (n.*28+28295C>G) c.2847C>G (p.Asp949Glu) c.2181C>G (p.Asp727Glu) | dbSNP |
| 7 | g.55201223C>T | CA4266232 | EGFR | c.2823C>T (p.Asp941=) c.900-4124C>T n.726C>T n.651C>T c.2982C>T (p.Asp994=) c.*28+28295C>T (n.*28+28295C>T) c.2847C>T (p.Asp949=) c.2181C>T (p.Asp727=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201224T>A | CA367582411 | EGFR | c.2824T>A (p.Ser942Thr) c.900-4123T>A n.727T>A n.652T>A c.2983T>A (p.Ser995Thr) c.*28+28296T>A (n.*28+28296T>A) c.2848T>A (p.Ser950Thr) c.2182T>A (p.Ser728Thr) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201224T>C | CA367582412 | EGFR | c.2824T>C (p.Ser942Pro) c.900-4123T>C n.727T>C n.652T>C c.2983T>C (p.Ser995Pro) c.*28+28296T>C (n.*28+28296T>C) c.2848T>C (p.Ser950Pro) c.2182T>C (p.Ser728Pro) | ClinVar dbSNP |
| 7 | g.55201224T>G | CA367582413 | EGFR | c.2824T>G (p.Ser942Ala) c.900-4123T>G n.727T>G n.652T>G c.2983T>G (p.Ser995Ala) c.*28+28296T>G (n.*28+28296T>G) c.2848T>G (p.Ser950Ala) c.2182T>G (p.Ser728Ala) | |
| 7 | g.55201225C>A | CA367582414 | EGFR | c.2825C>A (p.Ser942Tyr) c.900-4122C>A n.728C>A n.653C>A c.2984C>A (p.Ser995Tyr) c.*28+28297C>A (n.*28+28297C>A) c.2849C>A (p.Ser950Tyr) c.2183C>A (p.Ser728Tyr) | |
| 7 | g.55201225C= | CA1708928420 | EGFR | c.2825C= (p.Ser942=) c.900-4122C= n.728C= n.653C= c.2984C= (p.Ser995=) c.*28+28297C= (n.*28+28297C=) c.2849C= (p.Ser950=) c.2183C= (p.Ser728=) | |
| 7 | g.55201225C>G | CA158937832 | EGFR | c.2825C>G (p.Ser942Cys) c.900-4122C>G n.728C>G n.653C>G c.2984C>G (p.Ser995Cys) c.*28+28297C>G (n.*28+28297C>G) c.2849C>G (p.Ser950Cys) c.2183C>G (p.Ser728Cys) | dbSNP |
| 7 | g.55201225C>T | CA367582415 | EGFR | c.2825C>T (p.Ser942Phe) c.900-4122C>T n.728C>T n.653C>T c.2984C>T (p.Ser995Phe) c.*28+28297C>T (n.*28+28297C>T) c.2849C>T (p.Ser950Phe) c.2183C>T (p.Ser728Phe) | gnomAD v4 |
| 7 | g.55201226C>A | CA454968530 | EGFR | c.2826C>A (p.Ser942=) c.900-4121C>A n.729C>A n.654C>A c.2985C>A (p.Ser995=) c.*28+28298C>A (n.*28+28298C>A) c.2850C>A (p.Ser950=) c.2184C>A (p.Ser728=) | dbSNP |
| 7 | g.55201226C>G | CA454968531 | EGFR | c.2826C>G (p.Ser942=) c.900-4121C>G n.729C>G n.654C>G c.2985C>G (p.Ser995=) c.*28+28298C>G (n.*28+28298C>G) c.2850C>G (p.Ser950=) c.2184C>G (p.Ser728=) | dbSNP |
| 7 | g.55201226C>T | CA454968532 | EGFR | c.2826C>T (p.Ser942=) c.900-4121C>T n.729C>T n.654C>T c.2985C>T (p.Ser995=) c.*28+28298C>T (n.*28+28298C>T) c.2850C>T (p.Ser950=) c.2184C>T (p.Ser728=) | dbSNP |
| 7 | g.55201227A>C | CA367582418 | EGFR | c.2827A>C (p.Asn943His) c.900-4120A>C n.730A>C n.655A>C c.2986A>C (p.Asn996His) c.*28+28299A>C (n.*28+28299A>C) c.2851A>C (p.Asn951His) c.2185A>C (p.Asn729His) | |
| 7 | g.55201227A>G | CA367582416 | EGFR | c.2827A>G (p.Asn943Asp) c.900-4120A>G n.730A>G n.655A>G c.2986A>G (p.Asn996Asp) c.*28+28299A>G (n.*28+28299A>G) c.2851A>G (p.Asn951Asp) c.2185A>G (p.Asn729Asp) | dbSNP |
| 7 | g.55201227A>T | CA367582417 | EGFR | c.2827A>T (p.Asn943Tyr) c.900-4120A>T n.730A>T n.655A>T c.2986A>T (p.Asn996Tyr) c.*28+28299A>T (n.*28+28299A>T) c.2851A>T (p.Asn951Tyr) c.2185A>T (p.Asn729Tyr) | dbSNP |
| 7 | g.55201228A= | CA1708928421 | EGFR | c.2828A= (p.Asn943=) c.900-4119A= n.731A= n.656A= c.2987A= (p.Asn996=) c.*28+28300A= (n.*28+28300A=) c.2852A= (p.Asn951=) c.2186A= (p.Asn729=) | |
| 7 | g.55201228A>C | CA367582419 | EGFR | c.2828A>C (p.Asn943Thr) c.900-4119A>C n.731A>C n.656A>C c.2987A>C (p.Asn996Thr) c.*28+28300A>C (n.*28+28300A>C) c.2852A>C (p.Asn951Thr) c.2186A>C (p.Asn729Thr) | dbSNP |
| 7 | g.55201228A>G | CA4266233 | EGFR | c.2828A>G (p.Asn943Ser) c.900-4119A>G n.731A>G n.656A>G c.2987A>G (p.Asn996Ser) c.*28+28300A>G (n.*28+28300A>G) c.2852A>G (p.Asn951Ser) c.2186A>G (p.Asn729Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201228A>T | CA367582420 | EGFR | c.2828A>T (p.Asn943Ile) c.900-4119A>T n.731A>T n.656A>T c.2987A>T (p.Asn996Ile) c.*28+28300A>T (n.*28+28300A>T) c.2852A>T (p.Asn951Ile) c.2186A>T (p.Asn729Ile) | dbSNP |
| 7 | g.55201229C>A | CA4266234 | EGFR | c.2829C>A (p.Asn943Lys) c.900-4118C>A n.732C>A n.657C>A c.2988C>A (p.Asn996Lys) c.*28+28301C>A (n.*28+28301C>A) c.2853C>A (p.Asn951Lys) c.2187C>A (p.Asn729Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201229C= | CA1708928422 | EGFR | c.2829C= (p.Asn943=) c.900-4118C= n.732C= n.657C= c.2988C= (p.Asn996=) c.*28+28301C= (n.*28+28301C=) c.2853C= (p.Asn951=) c.2187C= (p.Asn729=) | |
| 7 | g.55201229C>G | CA367582421 | EGFR | c.2829C>G (p.Asn943Lys) c.900-4118C>G n.732C>G n.657C>G c.2988C>G (p.Asn996Lys) c.*28+28301C>G (n.*28+28301C>G) c.2853C>G (p.Asn951Lys) c.2187C>G (p.Asn729Lys) | dbSNP |
| 7 | g.55201229C>T | CA454968535 | EGFR | c.2829C>T (p.Asn943=) c.900-4118C>T n.732C>T n.657C>T c.2988C>T (p.Asn996=) c.*28+28301C>T (n.*28+28301C>T) c.2853C>T (p.Asn951=) c.2187C>T (p.Asn729=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201230T>A | CA367582422 | EGFR | c.2830T>A (p.Phe944Ile) c.900-4117T>A n.733T>A n.658T>A c.2989T>A (p.Phe997Ile) c.*28+28302T>A (n.*28+28302T>A) c.2854T>A (p.Phe952Ile) c.2188T>A (p.Phe730Ile) | dbSNP |
| 7 | g.55201230T>C | CA367582424 | EGFR | c.2830T>C (p.Phe944Leu) c.900-4117T>C n.733T>C n.658T>C c.2989T>C (p.Phe997Leu) c.*28+28302T>C (n.*28+28302T>C) c.2854T>C (p.Phe952Leu) c.2188T>C (p.Phe730Leu) | |
| 7 | g.55201230T>G | CA367582423 | EGFR | c.2830T>G (p.Phe944Val) c.900-4117T>G n.733T>G n.658T>G c.2989T>G (p.Phe997Val) c.*28+28302T>G (n.*28+28302T>G) c.2854T>G (p.Phe952Val) c.2188T>G (p.Phe730Val) | COSMIC |
| 7 | g.55201231T>A | CA367582425 | EGFR | c.2831T>A (p.Phe944Tyr) c.900-4116T>A n.734T>A n.659T>A c.2990T>A (p.Phe997Tyr) c.*28+28303T>A (n.*28+28303T>A) c.2855T>A (p.Phe952Tyr) c.2189T>A (p.Phe730Tyr) | dbSNP |
| 7 | g.55201231T>C | CA367582426 | EGFR | c.2831T>C (p.Phe944Ser) c.900-4116T>C n.734T>C n.659T>C c.2990T>C (p.Phe997Ser) c.*28+28303T>C (n.*28+28303T>C) c.2855T>C (p.Phe952Ser) c.2189T>C (p.Phe730Ser) | |
| 7 | g.55201231T>G | CA367582427 | EGFR | c.2831T>G (p.Phe944Cys) c.900-4116T>G n.734T>G n.659T>G c.2990T>G (p.Phe997Cys) c.*28+28303T>G (n.*28+28303T>G) c.2855T>G (p.Phe952Cys) c.2189T>G (p.Phe730Cys) | |
| 7 | g.55201232C>A | CA367582428 | EGFR | c.2832C>A (p.Phe944Leu) c.900-4115C>A n.735C>A n.660C>A c.2991C>A (p.Phe997Leu) c.*28+28304C>A (n.*28+28304C>A) c.2856C>A (p.Phe952Leu) c.2190C>A (p.Phe730Leu) | dbSNP |
| 7 | g.55201232C>G | CA367582429 | EGFR | c.2832C>G (p.Phe944Leu) c.900-4115C>G n.735C>G n.660C>G c.2991C>G (p.Phe997Leu) c.*28+28304C>G (n.*28+28304C>G) c.2856C>G (p.Phe952Leu) c.2190C>G (p.Phe730Leu) | dbSNP |
| 7 | g.55201232C>T | CA454968536 | EGFR | c.2832C>T (p.Phe944=) c.900-4115C>T n.735C>T n.660C>T c.2991C>T (p.Phe997=) c.*28+28304C>T (n.*28+28304C>T) c.2856C>T (p.Phe952=) c.2190C>T (p.Phe730=) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55201233T>A | CA367582430 | EGFR | c.2833T>A (p.Tyr945Asn) c.900-4114T>A n.736T>A n.661T>A c.2992T>A (p.Tyr998Asn) c.*28+28305T>A (n.*28+28305T>A) c.2857T>A (p.Tyr953Asn) c.2191T>A (p.Tyr731Asn) | dbSNP |
| 7 | g.55201233T>C | CA367582431 | EGFR | c.2833T>C (p.Tyr945His) c.900-4114T>C n.736T>C n.661T>C c.2992T>C (p.Tyr998His) c.*28+28305T>C (n.*28+28305T>C) c.2857T>C (p.Tyr953His) c.2191T>C (p.Tyr731His) | dbSNP gnomAD v4 |
| 7 | g.55201233T>G | CA367582432 | EGFR | c.2833T>G (p.Tyr945Asp) c.900-4114T>G n.736T>G n.661T>G c.2992T>G (p.Tyr998Asp) c.*28+28305T>G (n.*28+28305T>G) c.2857T>G (p.Tyr953Asp) c.2191T>G (p.Tyr731Asp) | |
| 7 | g.55201234A= | CA1708928423 | EGFR | c.2834A= (p.Tyr945=) c.900-4113A= n.737A= n.662A= c.2993A= (p.Tyr998=) c.*28+28306A= (n.*28+28306A=) c.2858A= (p.Tyr953=) c.2192A= (p.Tyr731=) | |
| 7 | g.55201234A>C | CA367582433 | EGFR | c.2834A>C (p.Tyr945Ser) c.900-4113A>C n.737A>C n.662A>C c.2993A>C (p.Tyr998Ser) c.*28+28306A>C (n.*28+28306A>C) c.2858A>C (p.Tyr953Ser) c.2192A>C (p.Tyr731Ser) | dbSNP |
| 7 | g.55201234A>G | CA367582434 | EGFR | c.2834A>G (p.Tyr945Cys) c.900-4113A>G n.737A>G n.662A>G c.2993A>G (p.Tyr998Cys) c.*28+28306A>G (n.*28+28306A>G) c.2858A>G (p.Tyr953Cys) c.2192A>G (p.Tyr731Cys) | ClinVar dbSNP |
| 7 | g.55201234A>T | CA367582435 | EGFR | c.2834A>T (p.Tyr945Phe) c.900-4113A>T n.737A>T n.662A>T c.2993A>T (p.Tyr998Phe) c.*28+28306A>T (n.*28+28306A>T) c.2858A>T (p.Tyr953Phe) c.2192A>T (p.Tyr731Phe) | dbSNP |
| 7 | g.55201235C>A | CA367582437 | EGFR | c.2835C>A (p.Tyr945Ter) c.900-4112C>A n.738C>A n.663C>A c.2994C>A (p.Tyr998Ter) c.*28+28307C>A (n.*28+28307C>A) c.2859C>A (p.Tyr953Ter) c.2193C>A (p.Tyr731Ter) | dbSNP |
| 7 | g.55201235C= | CA1708928424 | EGFR | c.2835C= (p.Tyr945=) c.900-4112C= n.738C= n.663C= c.2994C= (p.Tyr998=) c.*28+28307C= (n.*28+28307C=) c.2859C= (p.Tyr953=) c.2193C= (p.Tyr731=) | |
| 7 | g.55201235C>G | CA367582436 | EGFR | c.2835C>G (p.Tyr945Ter) c.900-4112C>G n.738C>G n.663C>G c.2994C>G (p.Tyr998Ter) c.*28+28307C>G (n.*28+28307C>G) c.2859C>G (p.Tyr953Ter) c.2193C>G (p.Tyr731Ter) | dbSNP |
| 7 | g.55201235C>T | CA454968538 | EGFR | c.2835C>T (p.Tyr945=) c.900-4112C>T n.738C>T n.663C>T c.2994C>T (p.Tyr998=) c.*28+28307C>T (n.*28+28307C>T) c.2859C>T (p.Tyr953=) c.2193C>T (p.Tyr731=) | ClinVar dbSNP |
| 7 | g.55201236C>A | CA367582438 | EGFR | c.2836C>A (p.Arg946Ser) c.900-4111C>A n.739C>A n.664C>A c.2995C>A (p.Arg999Ser) c.*28+28308C>A (n.*28+28308C>A) c.2860C>A (p.Arg954Ser) c.2194C>A (p.Arg732Ser) | dbSNP |
| 7 | g.55201236C= | CA1708928425 | EGFR | c.2836C= (p.Arg946=) c.900-4111C= n.739C= n.664C= c.2995C= (p.Arg999=) c.*28+28308C= (n.*28+28308C=) c.2860C= (p.Arg954=) c.2194C= (p.Arg732=) | |
| 7 | g.55201236C>G | CA367582439 | EGFR | c.2836C>G (p.Arg946Gly) c.900-4111C>G n.739C>G n.664C>G c.2995C>G (p.Arg999Gly) c.*28+28308C>G (n.*28+28308C>G) c.2860C>G (p.Arg954Gly) c.2194C>G (p.Arg732Gly) | dbSNP |
| 7 | g.55201236C>T | CA158937840 | EGFR | c.2836C>T (p.Arg946Cys) c.900-4111C>T n.739C>T n.664C>T c.2995C>T (p.Arg999Cys) c.*28+28308C>T (n.*28+28308C>T) c.2860C>T (p.Arg954Cys) c.2194C>T (p.Arg732Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201237G>A | CA4266235 | EGFR | c.2837G>A (p.Arg946His) c.900-4110G>A n.740G>A n.665G>A c.2996G>A (p.Arg999His) c.*28+28309G>A (n.*28+28309G>A) c.2861G>A (p.Arg954His) c.2195G>A (p.Arg732His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201237G>C | CA367582440 | EGFR | c.2837G>C (p.Arg946Pro) c.900-4110G>C n.740G>C n.665G>C c.2996G>C (p.Arg999Pro) c.*28+28309G>C (n.*28+28309G>C) c.2861G>C (p.Arg954Pro) c.2195G>C (p.Arg732Pro) | dbSNP |
| 7 | g.55201237G= | CA1708928426 | EGFR | c.2837G= (p.Arg946=) c.900-4110G= n.740G= n.665G= c.2996G= (p.Arg999=) c.*28+28309G= (n.*28+28309G=) c.2861G= (p.Arg954=) c.2195G= (p.Arg732=) | |
| 7 | g.55201237G>T | CA10624139 | EGFR | c.2837G>T (p.Arg946Leu) c.900-4110G>T n.740G>T n.665G>T c.2996G>T (p.Arg999Leu) c.*28+28309G>T (n.*28+28309G>T) c.2861G>T (p.Arg954Leu) c.2195G>T (p.Arg732Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201238T>A | CA454968542 | EGFR | c.2838T>A (p.Arg946=) c.900-4109T>A n.741T>A n.666T>A c.2997T>A (p.Arg999=) c.*28+28310T>A (n.*28+28310T>A) c.2862T>A (p.Arg954=) c.2196T>A (p.Arg732=) | dbSNP |
| 7 | g.55201238T>C | CA4266236 | EGFR | c.2838T>C (p.Arg946=) c.900-4109T>C n.741T>C n.666T>C c.2997T>C (p.Arg999=) c.*28+28310T>C (n.*28+28310T>C) c.2862T>C (p.Arg954=) c.2196T>C (p.Arg732=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201238T>G | CA454968540 | EGFR | c.2838T>G (p.Arg946=) c.900-4109T>G n.741T>G n.666T>G c.2997T>G (p.Arg999=) c.*28+28310T>G (n.*28+28310T>G) c.2862T>G (p.Arg954=) c.2196T>G (p.Arg732=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201238T= | CA1708928427 | EGFR | c.2838T= (p.Arg946=) c.900-4109T= n.741T= n.666T= c.2997T= (p.Arg999=) c.*28+28310T= (n.*28+28310T=) c.2862T= (p.Arg954=) c.2196T= (p.Arg732=) | |
| 7 | g.55201239G>A | CA367582441 | EGFR | c.2839G>A (p.Ala947Thr) c.900-4108G>A n.742G>A n.667G>A c.2998G>A (p.Ala1000Thr) c.*28+28311G>A (n.*28+28311G>A) c.2863G>A (p.Ala955Thr) c.2197G>A (p.Ala733Thr) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201239G>C | CA367582442 | EGFR | c.2839G>C (p.Ala947Pro) c.900-4108G>C n.742G>C n.667G>C c.2998G>C (p.Ala1000Pro) c.*28+28311G>C (n.*28+28311G>C) c.2863G>C (p.Ala955Pro) c.2197G>C (p.Ala733Pro) | dbSNP |
| 7 | g.55201239G>T | CA367582443 | EGFR | c.2839G>T (p.Ala947Ser) c.900-4108G>T n.742G>T n.667G>T c.2998G>T (p.Ala1000Ser) c.*28+28311G>T (n.*28+28311G>T) c.2863G>T (p.Ala955Ser) c.2197G>T (p.Ala733Ser) | dbSNP |
| 7 | g.55201240C>A | CA367582444 | EGFR | c.2840C>A (p.Ala947Asp) c.900-4107C>A n.743C>A n.668C>A c.2999C>A (p.Ala1000Asp) c.*28+28312C>A (n.*28+28312C>A) c.2864C>A (p.Ala955Asp) c.2198C>A (p.Ala733Asp) | ClinVar dbSNP |
| 7 | g.55201240C= | CA1708928428 | EGFR | c.2840C= (p.Ala947=) c.900-4107C= n.743C= n.668C= c.2999C= (p.Ala1000=) c.*28+28312C= (n.*28+28312C=) c.2864C= (p.Ala955=) c.2198C= (p.Ala733=) | |
| 7 | g.55201240C>G | CA367582445 | EGFR | c.2840C>G (p.Ala947Gly) c.900-4107C>G n.743C>G n.668C>G c.2999C>G (p.Ala1000Gly) c.*28+28312C>G (n.*28+28312C>G) c.2864C>G (p.Ala955Gly) c.2198C>G (p.Ala733Gly) | dbSNP |
| 7 | g.55201240C>T | CA367582446 | EGFR | c.2840C>T (p.Ala947Val) c.900-4107C>T n.743C>T n.668C>T c.2999C>T (p.Ala1000Val) c.*28+28312C>T (n.*28+28312C>T) c.2864C>T (p.Ala955Val) c.2198C>T (p.Ala733Val) | dbSNP gnomAD v4 |
| 7 | g.55201241C>A | CA454968546 | EGFR | c.2841C>A (p.Ala947=) c.900-4106C>A n.744C>A n.669C>A c.3000C>A (p.Ala1000=) c.*28+28313C>A (n.*28+28313C>A) c.2865C>A (p.Ala955=) c.2199C>A (p.Ala733=) | dbSNP |
| 7 | g.55201241C= | CA1708928429 | EGFR | c.2841C= (p.Ala947=) c.900-4106C= n.744C= n.669C= c.3000C= (p.Ala1000=) c.*28+28313C= (n.*28+28313C=) c.2865C= (p.Ala955=) c.2199C= (p.Ala733=) | |
| 7 | g.55201241C>G | CA454968544 | EGFR | c.2841C>G (p.Ala947=) c.900-4106C>G n.744C>G n.669C>G c.3000C>G (p.Ala1000=) c.*28+28313C>G (n.*28+28313C>G) c.2865C>G (p.Ala955=) c.2199C>G (p.Ala733=) | dbSNP |
| 7 | g.55201241C>T | CA454968545 | EGFR | c.2841C>T (p.Ala947=) c.900-4106C>T n.744C>T n.669C>T c.3000C>T (p.Ala1000=) c.*28+28313C>T (n.*28+28313C>T) c.2865C>T (p.Ala955=) c.2199C>T (p.Ala733=) | dbSNP |
| 7 | g.55201242C>A | CA367582447 | EGFR | c.2842C>A (p.Leu948Met) c.900-4105C>A n.745C>A n.670C>A c.3001C>A (p.Leu1001Met) c.*28+28314C>A (n.*28+28314C>A) c.2866C>A (p.Leu956Met) c.2200C>A (p.Leu734Met) | dbSNP |
| 7 | g.55201242C>G | CA367582448 | EGFR | c.2842C>G (p.Leu948Val) c.900-4105C>G n.745C>G n.670C>G c.3001C>G (p.Leu1001Val) c.*28+28314C>G (n.*28+28314C>G) c.2866C>G (p.Leu956Val) c.2200C>G (p.Leu734Val) | dbSNP |
| 7 | g.55201242C>T | CA454968547 | EGFR | c.2842C>T (p.Leu948=) c.900-4105C>T n.745C>T n.670C>T c.3001C>T (p.Leu1001=) c.*28+28314C>T (n.*28+28314C>T) c.2866C>T (p.Leu956=) c.2200C>T (p.Leu734=) | dbSNP |
| 7 | g.55201243T>A | CA367582451 | EGFR | c.2843T>A (p.Leu948Gln) c.900-4104T>A n.746T>A n.671T>A c.3002T>A (p.Leu1001Gln) c.*28+28315T>A (n.*28+28315T>A) c.2867T>A (p.Leu956Gln) c.2201T>A (p.Leu734Gln) | |
| 7 | g.55201243T>C | CA367582450 | EGFR | c.2843T>C (p.Leu948Pro) c.900-4104T>C n.746T>C n.671T>C c.3002T>C (p.Leu1001Pro) c.*28+28315T>C (n.*28+28315T>C) c.2867T>C (p.Leu956Pro) c.2201T>C (p.Leu734Pro) | |
| 7 | g.55201243T>G | CA367582449 | EGFR | c.2843T>G (p.Leu948Arg) c.900-4104T>G n.746T>G n.671T>G c.3002T>G (p.Leu1001Arg) c.*28+28315T>G (n.*28+28315T>G) c.2867T>G (p.Leu956Arg) c.2201T>G (p.Leu734Arg) | |
| 7 | g.55201244G>A | CA454968548 | EGFR | c.2844G>A (p.Leu948=) c.900-4103G>A n.747G>A n.672G>A c.3003G>A (p.Leu1001=) c.*28+28316G>A (n.*28+28316G>A) c.2868G>A (p.Leu956=) c.2202G>A (p.Leu734=) | ClinVar dbSNP |
| 7 | g.55201244G>C | CA454968550 | EGFR | c.2844G>C (p.Leu948=) c.900-4103G>C n.747G>C n.672G>C c.3003G>C (p.Leu1001=) c.*28+28316G>C (n.*28+28316G>C) c.2868G>C (p.Leu956=) c.2202G>C (p.Leu734=) | dbSNP |
| 7 | g.55201244G= | CA1708928430 | EGFR | c.2844G= (p.Leu948=) c.900-4103G= n.747G= n.672G= c.3003G= (p.Leu1001=) c.*28+28316G= (n.*28+28316G=) c.2868G= (p.Leu956=) c.2202G= (p.Leu734=) | |
| 7 | g.55201244G>T | CA454968549 | EGFR | c.2844G>T (p.Leu948=) c.900-4103G>T n.747G>T n.672G>T c.3003G>T (p.Leu1001=) c.*28+28316G>T (n.*28+28316G>T) c.2868G>T (p.Leu956=) c.2202G>T (p.Leu734=) | |
| 7 | g.55201245A= | CA1708928431 | EGFR | c.2845A= (p.Met949=) c.900-4102A= n.748A= n.673A= c.3004A= (p.Met1002=) c.*28+28317A= (n.*28+28317A=) c.2869A= (p.Met957=) c.2203A= (p.Met735=) | |
| 7 | g.55201245A>C | CA367582452 | EGFR | c.2845A>C (p.Met949Leu) c.900-4102A>C n.748A>C n.673A>C c.3004A>C (p.Met1002Leu) c.*28+28317A>C (n.*28+28317A>C) c.2869A>C (p.Met957Leu) c.2203A>C (p.Met735Leu) | |
| 7 | g.55201245A>G | CA367582453 | EGFR | c.2845A>G (p.Met949Val) c.900-4102A>G n.748A>G n.673A>G c.3004A>G (p.Met1002Val) c.*28+28317A>G (n.*28+28317A>G) c.2869A>G (p.Met957Val) c.2203A>G (p.Met735Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201245A>T | CA367582454 | EGFR | c.2845A>T (p.Met949Leu) c.900-4102A>T n.748A>T n.673A>T c.3004A>T (p.Met1002Leu) c.*28+28317A>T (n.*28+28317A>T) c.2869A>T (p.Met957Leu) c.2203A>T (p.Met735Leu) | dbSNP |
| 7 | g.55201246T>A | CA367582455 | EGFR | c.2846T>A (p.Met949Lys) c.900-4101T>A n.749T>A n.674T>A c.3005T>A (p.Met1002Lys) c.*28+28318T>A (n.*28+28318T>A) c.2870T>A (p.Met957Lys) c.2204T>A (p.Met735Lys) | |
| 7 | g.55201246T>C | CA367582456 | EGFR | c.2846T>C (p.Met949Thr) c.900-4101T>C n.749T>C n.674T>C c.3005T>C (p.Met1002Thr) c.*28+28318T>C (n.*28+28318T>C) c.2870T>C (p.Met957Thr) c.2204T>C (p.Met735Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201246T>G | CA367582457 | EGFR | c.2846T>G (p.Met949Arg) c.900-4101T>G n.749T>G n.674T>G c.3005T>G (p.Met1002Arg) c.*28+28318T>G (n.*28+28318T>G) c.2870T>G (p.Met957Arg) c.2204T>G (p.Met735Arg) | |
| 7 | g.55201246T= | CA1708928432 | EGFR | c.2846T= (p.Met949=) c.900-4101T= n.749T= n.674T= c.3005T= (p.Met1002=) c.*28+28318T= (n.*28+28318T=) c.2870T= (p.Met957=) c.2204T= (p.Met735=) | |
| 7 | g.55201247G>A | CA367582458 | EGFR | c.2847G>A (p.Met949Ile) c.900-4100G>A n.750G>A n.675G>A c.3006G>A (p.Met1002Ile) c.*28+28319G>A (n.*28+28319G>A) c.2871G>A (p.Met957Ile) c.2205G>A (p.Met735Ile) | ClinVar dbSNP |
| 7 | g.55201247G>C | CA367582459 | EGFR | c.2847G>C (p.Met949Ile) c.900-4100G>C n.750G>C n.675G>C c.3006G>C (p.Met1002Ile) c.*28+28319G>C (n.*28+28319G>C) c.2871G>C (p.Met957Ile) c.2205G>C (p.Met735Ile) | dbSNP |
| 7 | g.55201247G>T | CA367582460 | EGFR | c.2847G>T (p.Met949Ile) c.900-4100G>T n.750G>T n.675G>T c.3006G>T (p.Met1002Ile) c.*28+28319G>T (n.*28+28319G>T) c.2871G>T (p.Met957Ile) c.2205G>T (p.Met735Ile) | dbSNP COSMIC |
| 7 | g.55201247_55201248insCTCCTC | CA2682856341 | EGFR | c.2847_2848insCTCCTC (p.Met949_Asp950insLeuLeu) c.900-4100_900-4099insCTCCTC n.750_751insCTCCTC n.675_676insCTCCTC c.3006_3007insCTCCTC (p.Met1002_Asp1003insLeuLeu) c.*28+28319_*28+28320insCTCCTC (n.*28+28319_*28+28320insCTCCTC) c.2871_2872insCTCCTC (p.Met957_Asp958insLeuLeu) c.2205_2206insCTCCTC (p.Met735_Asp736insLeuLeu) | gnomAD v4 |
| 7 | g.55201248G>A | CA367582461 | EGFR | c.2848G>A (p.Asp950Asn) c.900-4099G>A n.751G>A n.676G>A c.3007G>A (p.Asp1003Asn) c.*28+28320G>A (n.*28+28320G>A) c.2872G>A (p.Asp958Asn) c.2206G>A (p.Asp736Asn) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201248G>C | CA367582462 | EGFR | c.2848G>C (p.Asp950His) c.900-4099G>C n.751G>C n.676G>C c.3007G>C (p.Asp1003His) c.*28+28320G>C (n.*28+28320G>C) c.2872G>C (p.Asp958His) c.2206G>C (p.Asp736His) | dbSNP |
| 7 | g.55201248G= | CA1708928433 | EGFR | c.2848G= (p.Asp950=) c.900-4099G= n.751G= n.676G= c.3007G= (p.Asp1003=) c.*28+28320G= (n.*28+28320G=) c.2872G= (p.Asp958=) c.2206G= (p.Asp736=) | |
| 7 | g.55201248G>T | CA367582463 | EGFR | c.2848G>T (p.Asp950Tyr) c.900-4099G>T n.751G>T n.676G>T c.3007G>T (p.Asp1003Tyr) c.*28+28320G>T (n.*28+28320G>T) c.2872G>T (p.Asp958Tyr) c.2206G>T (p.Asp736Tyr) | ClinVar dbSNP |
| 7 | g.55201249A>C | CA367582466 | EGFR | c.2849A>C (p.Asp950Ala) c.900-4098A>C n.752A>C n.677A>C c.3008A>C (p.Asp1003Ala) c.*28+28321A>C (n.*28+28321A>C) c.2873A>C (p.Asp958Ala) c.2207A>C (p.Asp736Ala) | |
| 7 | g.55201249A>G | CA367582465 | EGFR | c.2849A>G (p.Asp950Gly) c.900-4098A>G n.752A>G n.677A>G c.3008A>G (p.Asp1003Gly) c.*28+28321A>G (n.*28+28321A>G) c.2873A>G (p.Asp958Gly) c.2207A>G (p.Asp736Gly) | dbSNP |
| 7 | g.55201249A>T | CA367582464 | EGFR | c.2849A>T (p.Asp950Val) c.900-4098A>T n.752A>T n.677A>T c.3008A>T (p.Asp1003Val) c.*28+28321A>T (n.*28+28321A>T) c.2873A>T (p.Asp958Val) c.2207A>T (p.Asp736Val) | dbSNP |
| 7 | g.55201250T>A | CA367582467 | EGFR | c.2850T>A (p.Asp950Glu) c.900-4097T>A n.753T>A n.678T>A c.3009T>A (p.Asp1003Glu) c.*28+28322T>A (n.*28+28322T>A) c.2874T>A (p.Asp958Glu) c.2208T>A (p.Asp736Glu) | |
| 7 | g.55201250T>C | CA454968554 | EGFR | c.2850T>C (p.Asp950=) c.900-4097T>C n.753T>C n.678T>C c.3009T>C (p.Asp1003=) c.*28+28322T>C (n.*28+28322T>C) c.2874T>C (p.Asp958=) c.2208T>C (p.Asp736=) | gnomAD v4 |
| 7 | g.55201250T>G | CA367582468 | EGFR | c.2850T>G (p.Asp950Glu) c.900-4097T>G n.753T>G n.678T>G c.3009T>G (p.Asp1003Glu) c.*28+28322T>G (n.*28+28322T>G) c.2874T>G (p.Asp958Glu) c.2208T>G (p.Asp736Glu) | |
| 7 | g.55201250_55201253delinsTGAA | CA1708928434 | EGFR | c.2850_2853delinsTGAA (p.Asp950=) c.900-4097_900-4094delinsTGAA n.753_756delinsTGAA n.678_681delinsTGAA c.3009_3012delinsTGAA (p.Asp1003=) c.*28+28322_*28+28325delinsTGAA (n.*28+28322_*28+28325delinsTGAA) c.2874_2877delinsTGAA (p.Asp958=) c.2208_2211delinsTGAA (p.Asp736=) | |
| 7 | g.55201251G>A | CA367582469 | EGFR | c.2851G>A (p.Glu951Lys) c.900-4096G>A n.754G>A n.679G>A c.3010G>A (p.Glu1004Lys) c.*28+28323G>A (n.*28+28323G>A) c.2875G>A (p.Glu959Lys) c.2209G>A (p.Glu737Lys) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201251G>C | CA367582470 | EGFR | c.2851G>C (p.Glu951Gln) c.900-4096G>C n.754G>C n.679G>C c.3010G>C (p.Glu1004Gln) c.*28+28323G>C (n.*28+28323G>C) c.2875G>C (p.Glu959Gln) c.2209G>C (p.Glu737Gln) | dbSNP |
| 7 | g.55201251G>T | CA367582471 | EGFR | c.2851G>T (p.Glu951Ter) c.900-4096G>T n.754G>T n.679G>T c.3010G>T (p.Glu1004Ter) c.*28+28323G>T (n.*28+28323G>T) c.2875G>T (p.Glu959Ter) c.2209G>T (p.Glu737Ter) | |
| 7 | g.55201256_55201258dup | CA2739266427 | EGFR | c.2856_2858dup (p.Glu952_Asp953insGlu) c.900-4091_900-4089dup n.759_761dup n.684_686dup c.3015_3017dup (p.Glu1005_Asp1006insGlu) c.*28+28328_*28+28330dup (n.*28+28328_*28+28330dup) c.2880_2882dup (p.Glu960_Asp961insGlu) c.2214_2216dup (p.Glu738_Asp739insGlu) | ClinVar |
| 7 | g.55201256_55201258del | CA4266237 | EGFR | c.2856_2858del (p.Glu952del) c.900-4091_900-4089del n.759_761del n.684_686del c.3015_3017del (p.Glu1005del) c.*28+28328_*28+28330del (n.*28+28328_*28+28330del) c.2880_2882del (p.Glu960del) c.2214_2216del (p.Glu738del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201252A>C | CA367582474 | EGFR | c.2852A>C (p.Glu951Ala) c.900-4095A>C n.755A>C n.680A>C c.3011A>C (p.Glu1004Ala) c.*28+28324A>C (n.*28+28324A>C) c.2876A>C (p.Glu959Ala) c.2210A>C (p.Glu737Ala) | |
| 7 | g.55201252A>G | CA367582472 | EGFR | c.2852A>G (p.Glu951Gly) c.900-4095A>G n.755A>G n.680A>G c.3011A>G (p.Glu1004Gly) c.*28+28324A>G (n.*28+28324A>G) c.2876A>G (p.Glu959Gly) c.2210A>G (p.Glu737Gly) | dbSNP |
| 7 | g.55201252A>T | CA367582473 | EGFR | c.2852A>T (p.Glu951Val) c.900-4095A>T n.755A>T n.680A>T c.3011A>T (p.Glu1004Val) c.*28+28324A>T (n.*28+28324A>T) c.2876A>T (p.Glu959Val) c.2210A>T (p.Glu737Val) | dbSNP |
| 7 | g.55201253A>C | CA367582475 | EGFR | c.2853A>C (p.Glu951Asp) c.900-4094A>C n.756A>C n.681A>C c.3012A>C (p.Glu1004Asp) c.*28+28325A>C (n.*28+28325A>C) c.2877A>C (p.Glu959Asp) c.2211A>C (p.Glu737Asp) | |
| 7 | g.55201253A>G | CA454968558 | EGFR | c.2853A>G (p.Glu951=) c.900-4094A>G n.756A>G n.681A>G c.3012A>G (p.Glu1004=) c.*28+28325A>G (n.*28+28325A>G) c.2877A>G (p.Glu959=) c.2211A>G (p.Glu737=) | dbSNP |
| 7 | g.55201253A>T | CA367582476 | EGFR | c.2853A>T (p.Glu951Asp) c.900-4094A>T n.756A>T n.681A>T c.3012A>T (p.Glu1004Asp) c.*28+28325A>T (n.*28+28325A>T) c.2877A>T (p.Glu959Asp) c.2211A>T (p.Glu737Asp) | dbSNP |
| 7 | g.55201254G>A | CA367582477 | EGFR | c.2854G>A (p.Glu952Lys) c.900-4093G>A n.757G>A n.682G>A c.3013G>A (p.Glu1005Lys) c.*28+28326G>A (n.*28+28326G>A) c.2878G>A (p.Glu960Lys) c.2212G>A (p.Glu738Lys) | dbSNP gnomAD v4 |
| 7 | g.55201254G>C | CA367582478 | EGFR | c.2854G>C (p.Glu952Gln) c.900-4093G>C n.757G>C n.682G>C c.3013G>C (p.Glu1005Gln) c.*28+28326G>C (n.*28+28326G>C) c.2878G>C (p.Glu960Gln) c.2212G>C (p.Glu738Gln) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201254G>T | CA367582479 | EGFR | c.2854G>T (p.Glu952Ter) c.900-4093G>T n.757G>T n.682G>T c.3013G>T (p.Glu1005Ter) c.*28+28326G>T (n.*28+28326G>T) c.2878G>T (p.Glu960Ter) c.2212G>T (p.Glu738Ter) | dbSNP |
| 7 | g.55201255A= | CA1708928435 | EGFR | c.2855A= (p.Glu952=) c.900-4092A= n.758A= n.683A= c.3014A= (p.Glu1005=) c.*28+28327A= (n.*28+28327A=) c.2879A= (p.Glu960=) c.2213A= (p.Glu738=) | |
| 7 | g.55201255A>C | CA367582480 | EGFR | c.2855A>C (p.Glu952Ala) c.900-4092A>C n.758A>C n.683A>C c.3014A>C (p.Glu1005Ala) c.*28+28327A>C (n.*28+28327A>C) c.2879A>C (p.Glu960Ala) c.2213A>C (p.Glu738Ala) | |
| 7 | g.55201255A>G | CA367582482 | EGFR | c.2855A>G (p.Glu952Gly) c.900-4092A>G n.758A>G n.683A>G c.3014A>G (p.Glu1005Gly) c.*28+28327A>G (n.*28+28327A>G) c.2879A>G (p.Glu960Gly) c.2213A>G (p.Glu738Gly) | |
| 7 | g.55201255A>T | CA367582481 | EGFR | c.2855A>T (p.Glu952Val) c.900-4092A>T n.758A>T n.683A>T c.3014A>T (p.Glu1005Val) c.*28+28327A>T (n.*28+28327A>T) c.2879A>T (p.Glu960Val) c.2213A>T (p.Glu738Val) | ClinVar dbSNP |
| 7 | g.55201256A= | CA1708928436 | EGFR | c.2856A= (p.Glu952=) c.900-4091A= n.759A= n.684A= c.3015A= (p.Glu1005=) c.*28+28328A= (n.*28+28328A=) c.2880A= (p.Glu960=) c.2214A= (p.Glu738=) | |
| 7 | g.55201256A>C | CA367582483 | EGFR | c.2856A>C (p.Glu952Asp) c.900-4091A>C n.759A>C n.684A>C c.3015A>C (p.Glu1005Asp) c.*28+28328A>C (n.*28+28328A>C) c.2880A>C (p.Glu960Asp) c.2214A>C (p.Glu738Asp) | |
| 7 | g.55201256A>G | CA4266238 | EGFR | c.2856A>G (p.Glu952=) c.900-4091A>G n.759A>G n.684A>G c.3015A>G (p.Glu1005=) c.*28+28328A>G (n.*28+28328A>G) c.2880A>G (p.Glu960=) c.2214A>G (p.Glu738=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201256A>T | CA367582484 | EGFR | c.2856A>T (p.Glu952Asp) c.900-4091A>T n.759A>T n.684A>T c.3015A>T (p.Glu1005Asp) c.*28+28328A>T (n.*28+28328A>T) c.2880A>T (p.Glu960Asp) c.2214A>T (p.Glu738Asp) | dbSNP |
| 7 | g.55201257G>A | CA367582485 | EGFR | c.2857G>A (p.Asp953Asn) c.900-4090G>A n.760G>A n.685G>A c.3016G>A (p.Asp1006Asn) c.*28+28329G>A (n.*28+28329G>A) c.2881G>A (p.Asp961Asn) c.2215G>A (p.Asp739Asn) | dbSNP |
| 7 | g.55201257G>C | CA367582486 | EGFR | c.2857G>C (p.Asp953His) c.900-4090G>C n.760G>C n.685G>C c.3016G>C (p.Asp1006His) c.*28+28329G>C (n.*28+28329G>C) c.2881G>C (p.Asp961His) c.2215G>C (p.Asp739His) | ClinVar dbSNP |
| 7 | g.55201257G= | CA1708928437 | EGFR | c.2857G= (p.Asp953=) c.900-4090G= n.760G= n.685G= c.3016G= (p.Asp1006=) c.*28+28329G= (n.*28+28329G=) c.2881G= (p.Asp961=) c.2215G= (p.Asp739=) | |
| 7 | g.55201257G>T | CA367582487 | EGFR | c.2857G>T (p.Asp953Tyr) c.900-4090G>T n.760G>T n.685G>T c.3016G>T (p.Asp1006Tyr) c.*28+28329G>T (n.*28+28329G>T) c.2881G>T (p.Asp961Tyr) c.2215G>T (p.Asp739Tyr) | |
| 7 | g.55201258A= | CA1708928438 | EGFR | c.2858A= (p.Asp953=) c.900-4089A= n.761A= n.686A= c.3017A= (p.Asp1006=) c.*28+28330A= (n.*28+28330A=) c.2882A= (p.Asp961=) c.2216A= (p.Asp739=) | |
| 7 | g.55201258A>C | CA4266239 | EGFR | c.2858A>C (p.Asp953Ala) c.900-4089A>C n.761A>C n.686A>C c.3017A>C (p.Asp1006Ala) c.*28+28330A>C (n.*28+28330A>C) c.2882A>C (p.Asp961Ala) c.2216A>C (p.Asp739Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201258A>G | CA367582488 | EGFR | c.2858A>G (p.Asp953Gly) c.900-4089A>G n.761A>G n.686A>G c.3017A>G (p.Asp1006Gly) c.*28+28330A>G (n.*28+28330A>G) c.2882A>G (p.Asp961Gly) c.2216A>G (p.Asp739Gly) | dbSNP gnomAD v4 |
| 7 | g.55201258A>T | CA367582489 | EGFR | c.2858A>T (p.Asp953Val) c.900-4089A>T n.761A>T n.686A>T c.3017A>T (p.Asp1006Val) c.*28+28330A>T (n.*28+28330A>T) c.2882A>T (p.Asp961Val) c.2216A>T (p.Asp739Val) | dbSNP gnomAD v4 |
| 7 | g.55201259C>A | CA367582490 | EGFR | c.2859C>A (p.Asp953Glu) c.900-4088C>A n.762C>A n.687C>A c.3018C>A (p.Asp1006Glu) c.*28+28331C>A (n.*28+28331C>A) c.2883C>A (p.Asp961Glu) c.2217C>A (p.Asp739Glu) | dbSNP |
| 7 | g.55201259C= | CA1708928439 | EGFR | c.2859C= (p.Asp953=) c.900-4088C= n.762C= n.687C= c.3018C= (p.Asp1006=) c.*28+28331C= (n.*28+28331C=) c.2883C= (p.Asp961=) c.2217C= (p.Asp739=) | |
| 7 | g.55201259C>G | CA367582491 | EGFR | c.2859C>G (p.Asp953Glu) c.900-4088C>G n.762C>G n.687C>G c.3018C>G (p.Asp1006Glu) c.*28+28331C>G (n.*28+28331C>G) c.2883C>G (p.Asp961Glu) c.2217C>G (p.Asp739Glu) | dbSNP |
| 7 | g.55201259C>T | CA454968561 | EGFR | c.2859C>T (p.Asp953=) c.900-4088C>T n.762C>T n.687C>T c.3018C>T (p.Asp1006=) c.*28+28331C>T (n.*28+28331C>T) c.2883C>T (p.Asp961=) c.2217C>T (p.Asp739=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201260A= | CA1708928440 | EGFR | c.2860A= (p.Met954=) c.900-4087A= n.763A= n.688A= c.3019A= (p.Met1007=) c.*28+28332A= (n.*28+28332A=) c.2884A= (p.Met962=) c.2218A= (p.Met740=) | |
| 7 | g.55201260A>C | CA367582494 | EGFR | c.2860A>C (p.Met954Leu) c.900-4087A>C n.763A>C n.688A>C c.3019A>C (p.Met1007Leu) c.*28+28332A>C (n.*28+28332A>C) c.2884A>C (p.Met962Leu) c.2218A>C (p.Met740Leu) | |
| 7 | g.55201260A>G | CA367582493 | EGFR | c.2860A>G (p.Met954Val) c.900-4087A>G n.763A>G n.688A>G c.3019A>G (p.Met1007Val) c.*28+28332A>G (n.*28+28332A>G) c.2884A>G (p.Met962Val) c.2218A>G (p.Met740Val) | ClinVar dbSNP |
| 7 | g.55201260A>T | CA367582492 | EGFR | c.2860A>T (p.Met954Leu) c.900-4087A>T n.763A>T n.688A>T c.3019A>T (p.Met1007Leu) c.*28+28332A>T (n.*28+28332A>T) c.2884A>T (p.Met962Leu) c.2218A>T (p.Met740Leu) | ClinVar dbSNP |
| 7 | g.55201261T>A | CA367582495 | EGFR | c.2861T>A (p.Met954Lys) c.900-4086T>A n.764T>A n.689T>A c.3020T>A (p.Met1007Lys) c.*28+28333T>A (n.*28+28333T>A) c.2885T>A (p.Met962Lys) c.2219T>A (p.Met740Lys) | |
| 7 | g.55201261T>C | CA367582497 | EGFR | c.2861T>C (p.Met954Thr) c.900-4086T>C n.764T>C n.689T>C c.3020T>C (p.Met1007Thr) c.*28+28333T>C (n.*28+28333T>C) c.2885T>C (p.Met962Thr) c.2219T>C (p.Met740Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201261T>G | CA367582496 | EGFR | c.2861T>G (p.Met954Arg) c.900-4086T>G n.764T>G n.689T>G c.3020T>G (p.Met1007Arg) c.*28+28333T>G (n.*28+28333T>G) c.2885T>G (p.Met962Arg) c.2219T>G (p.Met740Arg) | |
| 7 | g.55201261T= | CA1708928441 | EGFR | c.2861T= (p.Met954=) c.900-4086T= n.764T= n.689T= c.3020T= (p.Met1007=) c.*28+28333T= (n.*28+28333T=) c.2885T= (p.Met962=) c.2219T= (p.Met740=) | |
| 7 | g.55201262G>A | CA367582498 | EGFR | c.2862G>A (p.Met954Ile) c.900-4085G>A n.765G>A n.690G>A c.3021G>A (p.Met1007Ile) c.*28+28334G>A (n.*28+28334G>A) c.2886G>A (p.Met962Ile) c.2220G>A (p.Met740Ile) | |
| 7 | g.55201262G>C | CA367582500 | EGFR | c.2862G>C (p.Met954Ile) c.900-4085G>C n.765G>C n.690G>C c.3021G>C (p.Met1007Ile) c.*28+28334G>C (n.*28+28334G>C) c.2886G>C (p.Met962Ile) c.2220G>C (p.Met740Ile) | |
| 7 | g.55201262G>T | CA367582499 | EGFR | c.2862G>T (p.Met954Ile) c.900-4085G>T n.765G>T n.690G>T c.3021G>T (p.Met1007Ile) c.*28+28334G>T (n.*28+28334G>T) c.2886G>T (p.Met962Ile) c.2220G>T (p.Met740Ile) | |
| 7 | g.55201263G>A | CA367582501 | EGFR | c.2863G>A (p.Asp955Asn) c.900-4084G>A n.766G>A n.691G>A c.3022G>A (p.Asp1008Asn) c.*28+28335G>A (n.*28+28335G>A) c.2887G>A (p.Asp963Asn) c.2221G>A (p.Asp741Asn) | ClinVar dbSNP |
| 7 | g.55201263G>C | CA367582503 | EGFR | c.2863G>C (p.Asp955His) c.900-4084G>C n.766G>C n.691G>C c.3022G>C (p.Asp1008His) c.*28+28335G>C (n.*28+28335G>C) c.2887G>C (p.Asp963His) c.2221G>C (p.Asp741His) | dbSNP |
| 7 | g.55201263G= | CA1708928442 | EGFR | c.2863G= (p.Asp955=) c.900-4084G= n.766G= n.691G= c.3022G= (p.Asp1008=) c.*28+28335G= (n.*28+28335G=) c.2887G= (p.Asp963=) c.2221G= (p.Asp741=) | |
| 7 | g.55201263G>T | CA367582502 | EGFR | c.2863G>T (p.Asp955Tyr) c.900-4084G>T n.766G>T n.691G>T c.3022G>T (p.Asp1008Tyr) c.*28+28335G>T (n.*28+28335G>T) c.2887G>T (p.Asp963Tyr) c.2221G>T (p.Asp741Tyr) | dbSNP |
| 7 | g.55201264A= | CA1708928443 | EGFR | c.2864A= (p.Asp955=) c.900-4083A= n.767A= n.692A= c.3023A= (p.Asp1008=) c.*28+28336A= (n.*28+28336A=) c.2888A= (p.Asp963=) c.2222A= (p.Asp741=) | |
| 7 | g.55201264A>C | CA367582504 | EGFR | c.2864A>C (p.Asp955Ala) c.900-4083A>C n.767A>C n.692A>C c.3023A>C (p.Asp1008Ala) c.*28+28336A>C (n.*28+28336A>C) c.2888A>C (p.Asp963Ala) c.2222A>C (p.Asp741Ala) | dbSNP |
| 7 | g.55201264A>G | CA367582506 | EGFR | c.2864A>G (p.Asp955Gly) c.900-4083A>G n.767A>G n.692A>G c.3023A>G (p.Asp1008Gly) c.*28+28336A>G (n.*28+28336A>G) c.2888A>G (p.Asp963Gly) c.2222A>G (p.Asp741Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201264A>T | CA367582505 | EGFR | c.2864A>T (p.Asp955Val) c.900-4083A>T n.767A>T n.692A>T c.3023A>T (p.Asp1008Val) c.*28+28336A>T (n.*28+28336A>T) c.2888A>T (p.Asp963Val) c.2222A>T (p.Asp741Val) | dbSNP |
| 7 | g.55201265C>A | CA4266240 | EGFR | c.2865C>A (p.Asp955Glu) c.900-4082C>A n.768C>A n.693C>A c.3024C>A (p.Asp1008Glu) c.*28+28337C>A (n.*28+28337C>A) c.2889C>A (p.Asp963Glu) c.2223C>A (p.Asp741Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201265C= | CA1708928444 | EGFR | c.2865C= (p.Asp955=) c.900-4082C= n.768C= n.693C= c.3024C= (p.Asp1008=) c.*28+28337C= (n.*28+28337C=) c.2889C= (p.Asp963=) c.2223C= (p.Asp741=) | |
| 7 | g.55201265C>G | CA367582507 | EGFR | c.2865C>G (p.Asp955Glu) c.900-4082C>G n.768C>G n.693C>G c.3024C>G (p.Asp1008Glu) c.*28+28337C>G (n.*28+28337C>G) c.2889C>G (p.Asp963Glu) c.2223C>G (p.Asp741Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201265C>T | CA158937860 | EGFR | c.2865C>T (p.Asp955=) c.900-4082C>T n.768C>T n.693C>T c.3024C>T (p.Asp1008=) c.*28+28337C>T (n.*28+28337C>T) c.2889C>T (p.Asp963=) c.2223C>T (p.Asp741=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201266G>A | CA4266241 | EGFR | c.2866G>A (p.Asp956Asn) c.900-4081G>A n.769G>A n.694G>A c.3025G>A (p.Asp1009Asn) c.*28+28338G>A (n.*28+28338G>A) c.2890G>A (p.Asp964Asn) c.2224G>A (p.Asp742Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55201266G>C | CA367582508 | EGFR | c.2866G>C (p.Asp956His) c.900-4081G>C n.769G>C n.694G>C c.3025G>C (p.Asp1009His) c.*28+28338G>C (n.*28+28338G>C) c.2890G>C (p.Asp964His) c.2224G>C (p.Asp742His) | dbSNP |
| 7 | g.55201266G= | CA1708928445 | EGFR | c.2866G= (p.Asp956=) c.900-4081G= n.769G= n.694G= c.3025G= (p.Asp1009=) c.*28+28338G= (n.*28+28338G=) c.2890G= (p.Asp964=) c.2224G= (p.Asp742=) | |
| 7 | g.55201266G>T | CA367582509 | EGFR | c.2866G>T (p.Asp956Tyr) c.900-4081G>T n.769G>T n.694G>T c.3025G>T (p.Asp1009Tyr) c.*28+28338G>T (n.*28+28338G>T) c.2890G>T (p.Asp964Tyr) c.2224G>T (p.Asp742Tyr) | |
| 7 | g.55201267A>C | CA367582510 | EGFR | c.2867A>C (p.Asp956Ala) c.900-4080A>C n.770A>C n.695A>C c.3026A>C (p.Asp1009Ala) c.*28+28339A>C (n.*28+28339A>C) c.2891A>C (p.Asp964Ala) c.2225A>C (p.Asp742Ala) | dbSNP |
| 7 | g.55201267A>G | CA367582511 | EGFR | c.2867A>G (p.Asp956Gly) c.900-4080A>G n.770A>G n.695A>G c.3026A>G (p.Asp1009Gly) c.*28+28339A>G (n.*28+28339A>G) c.2891A>G (p.Asp964Gly) c.2225A>G (p.Asp742Gly) | dbSNP |
| 7 | g.55201267A>T | CA367582512 | EGFR | c.2867A>T (p.Asp956Val) c.900-4080A>T n.770A>T n.695A>T c.3026A>T (p.Asp1009Val) c.*28+28339A>T (n.*28+28339A>T) c.2891A>T (p.Asp964Val) c.2225A>T (p.Asp742Val) | dbSNP |