UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.127738347_127738349del | CA4875228 | MYC | c.85_87del (p.Glu29del) c.127_129del (p.Glu43del) c.130_132del (p.Glu44del) c.-216_-214del (n.-216_-214del) c.51_53del (p.Arg18del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738344G>A | CA372279390 | MYC | c.82G>A (p.Glu28Lys) c.124G>A (p.Glu42Lys) c.127G>A (p.Glu43Lys) c.-219G>A (n.-219G>A) c.48G>A (p.Arg16=) | dbSNP |
| 8 | g.127738344G>C | CA372279388 | MYC | c.82G>C (p.Glu28Gln) c.124G>C (p.Glu42Gln) c.127G>C (p.Glu43Gln) c.-219G>C (n.-219G>C) c.48G>C (p.Arg16Ser) | dbSNP |
| 8 | g.127738344G>T | CA372279389 | MYC | c.82G>T (p.Glu28Ter) c.124G>T (p.Glu42Ter) c.127G>T (p.Glu43Ter) c.-219G>T (n.-219G>T) c.48G>T (p.Arg16Ser) | dbSNP |
| 8 | g.127738345A>C | CA372279391 | MYC | c.83A>C (p.Glu28Ala) c.125A>C (p.Glu42Ala) c.128A>C (p.Glu43Ala) c.-218A>C (n.-218A>C) c.49A>C (p.Arg17=) | |
| 8 | g.127738345A>G | CA372279392 | MYC | c.83A>G (p.Glu28Gly) c.125A>G (p.Glu42Gly) c.128A>G (p.Glu43Gly) c.-218A>G (n.-218A>G) c.49A>G (p.Arg17Gly) | |
| 8 | g.127738345A>T | CA372279393 | MYC | c.83A>T (p.Glu28Val) c.125A>T (p.Glu42Val) c.128A>T (p.Glu43Val) c.-218A>T (n.-218A>T) c.49A>T (p.Arg17Trp) | |
| 8 | g.127738346G>A | CA372279394 | MYC | c.84G>A (p.Glu28=) c.126G>A (p.Glu42=) c.129G>A (p.Glu43=) c.-217G>A (n.-217G>A) c.50G>A (p.Arg17Lys) | dbSNP gnomAD v4 |
| 8 | g.127738346G>C | CA372279395 | MYC | c.84G>C (p.Glu28Asp) c.126G>C (p.Glu42Asp) c.129G>C (p.Glu43Asp) c.-217G>C (n.-217G>C) c.50G>C (p.Arg17Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738346G= | CA1818466252 | MYC | c.84G= (p.Glu28=) c.126G= (p.Glu42=) c.129G= (p.Glu43=) c.-217G= (n.-217G=) c.50G= (p.Arg17=) | |
| 8 | g.127738346G>T | CA372279396 | MYC | c.84G>T (p.Glu28Asp) c.126G>T (p.Glu42Asp) c.129G>T (p.Glu43Asp) c.-217G>T (n.-217G>T) c.50G>T (p.Arg17Met) | |
| 8 | g.127738347G>A | CA372279397 | MYC | c.85G>A (p.Glu29Lys) c.127G>A (p.Glu43Lys) c.130G>A (p.Glu44Lys) c.-216G>A (n.-216G>A) c.51G>A (p.Arg17=) | |
| 8 | g.127738347G>C | CA372279398 | MYC | c.85G>C (p.Glu29Gln) c.127G>C (p.Glu43Gln) c.130G>C (p.Glu44Gln) c.-216G>C (n.-216G>C) c.51G>C (p.Arg17Ser) | |
| 8 | g.127738347G>T | CA372279399 | MYC | c.85G>T (p.Glu29Ter) c.127G>T (p.Glu43Ter) c.130G>T (p.Glu44Ter) c.-216G>T (n.-216G>T) c.51G>T (p.Arg17Ser) | dbSNP |
| 8 | g.127738348A>C | CA372279400 | MYC | c.86A>C (p.Glu29Ala) c.128A>C (p.Glu43Ala) c.131A>C (p.Glu44Ala) c.-215A>C (n.-215A>C) c.52A>C (p.Arg18=) | |
| 8 | g.127738348A>G | CA372279401 | MYC | c.86A>G (p.Glu29Gly) c.128A>G (p.Glu43Gly) c.131A>G (p.Glu44Gly) c.-215A>G (n.-215A>G) c.52A>G (p.Arg18Gly) | dbSNP |
| 8 | g.127738348A>T | CA372279402 | MYC | c.86A>T (p.Glu29Val) c.128A>T (p.Glu43Val) c.131A>T (p.Glu44Val) c.-215A>T (n.-215A>T) c.52A>T (p.Arg18Ter) | dbSNP |
| 8 | g.127738349G>A | CA4875229 | MYC | c.87G>A (p.Glu29=) c.129G>A (p.Glu43=) c.132G>A (p.Glu44=) c.-214G>A (n.-214G>A) c.53G>A (p.Arg18Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738349G>C | CA4875230 | MYC | c.87G>C (p.Glu29Asp) c.129G>C (p.Glu43Asp) c.132G>C (p.Glu44Asp) c.-214G>C (n.-214G>C) c.53G>C (p.Arg18Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738349G= | CA1818466256 | MYC | c.87G= (p.Glu29=) c.129G= (p.Glu43=) c.132G= (p.Glu44=) c.-214G= (n.-214G=) c.53G= (p.Arg18=) | |
| 8 | g.127738349G>T | CA372279403 | MYC | c.87G>T (p.Glu29Asp) c.129G>T (p.Glu43Asp) c.132G>T (p.Glu44Asp) c.-214G>T (n.-214G>T) c.53G>T (p.Arg18Ile) | dbSNP |
| 8 | g.127738350A>C | CA372279404 | MYC | c.88A>C (p.Asn30His) c.130A>C (p.Asn44His) c.133A>C (p.Asn45His) c.-213A>C (n.-213A>C) c.54A>C (p.Arg18Ser) | |
| 8 | g.127738350A>G | CA372279405 | MYC | c.88A>G (p.Asn30Asp) c.130A>G (p.Asn44Asp) c.133A>G (p.Asn45Asp) c.-213A>G (n.-213A>G) c.54A>G (p.Arg18=) | |
| 8 | g.127738350A>T | CA372279406 | MYC | c.88A>T (p.Asn30Tyr) c.130A>T (p.Asn44Tyr) c.133A>T (p.Asn45Tyr) c.-213A>T (n.-213A>T) c.54A>T (p.Arg18Ser) | dbSNP |
| 8 | g.127738351A= | CA1818466264 | MYC | c.89A= (p.Asn30=) c.131A= (p.Asn44=) c.134A= (p.Asn45=) c.-212A= (n.-212A=) c.55A= (p.Thr19=) | |
| 8 | g.127738351A>C | CA372279407 | MYC | c.89A>C (p.Asn30Thr) c.131A>C (p.Asn44Thr) c.134A>C (p.Asn45Thr) c.-212A>C (n.-212A>C) c.55A>C (p.Thr19Pro) | |
| 8 | g.127738351A>G | CA372279408 | MYC | c.89A>G (p.Asn30Ser) c.131A>G (p.Asn44Ser) c.134A>G (p.Asn45Ser) c.-212A>G (n.-212A>G) c.55A>G (p.Thr19Ala) | dbSNP |
| 8 | g.127738351A>T | CA372279409 | MYC | c.89A>T (p.Asn30Ile) c.131A>T (p.Asn44Ile) c.134A>T (p.Asn45Ile) c.-212A>T (n.-212A>T) c.55A>T (p.Thr19Ser) | dbSNP |
| 8 | g.127738351_127738354delinsACTT | CA1818466263 | MYC | c.89_92delinsACTT (p.Asn30=) c.131_134delinsACTT (p.Asn44=) c.134_137delinsACTT (p.Asn45=) c.-212_-209delinsACTT (n.-212_-209delinsACTT) c.55_58delinsACTT (p.Thr19=) | |
| 8 | g.127738352C>A | CA372279411 | MYC | c.90C>A (p.Asn30Lys) c.132C>A (p.Asn44Lys) c.135C>A (p.Asn45Lys) c.-211C>A (n.-211C>A) c.56C>A (p.Thr19Asn) | dbSNP |
| 8 | g.127738352C>G | CA372279410 | MYC | c.90C>G (p.Asn30Lys) c.132C>G (p.Asn44Lys) c.135C>G (p.Asn45Lys) c.-211C>G (n.-211C>G) c.56C>G (p.Thr19Ser) | dbSNP |
| 8 | g.127738352C>T | CA372279412 | MYC | c.90C>T (p.Asn30=) c.132C>T (p.Asn44=) c.135C>T (p.Asn45=) c.-211C>T (n.-211C>T) c.56C>T (p.Thr19Ile) | dbSNP COSMIC COSMIC |
| 8 | g.127738354_127738356del | CA4875231 | MYC | c.92_94del (p.Phe31del) c.134_136del (p.Phe45del) c.137_139del (p.Phe46del) c.-209_-207del (n.-209_-207del) c.58_60del (p.Ser20del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738353T>A | CA372279413 | MYC | c.91T>A (p.Phe31Ile) c.133T>A (p.Phe45Ile) c.136T>A (p.Phe46Ile) c.-210T>A (n.-210T>A) c.57T>A (p.Thr19=) | |
| 8 | g.127738353T>C | CA372279414 | MYC | c.91T>C (p.Phe31Leu) c.133T>C (p.Phe45Leu) c.136T>C (p.Phe46Leu) c.-210T>C (n.-210T>C) c.57T>C (p.Thr19=) | COSMIC COSMIC |
| 8 | g.127738353T>G | CA372279415 | MYC | c.91T>G (p.Phe31Val) c.133T>G (p.Phe45Val) c.136T>G (p.Phe46Val) c.-210T>G (n.-210T>G) c.57T>G (p.Thr19=) | |
| 8 | g.127738354T>A | CA372279416 | MYC | c.92T>A (p.Phe31Tyr) c.134T>A (p.Phe45Tyr) c.137T>A (p.Phe46Tyr) c.-209T>A (n.-209T>A) c.58T>A (p.Ser20Thr) | |
| 8 | g.127738354T>C | CA4875232 | MYC | c.92T>C (p.Phe31Ser) c.134T>C (p.Phe45Ser) c.137T>C (p.Phe46Ser) c.-209T>C (n.-209T>C) c.58T>C (p.Ser20Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738354T>G | CA372279417 | MYC | c.92T>G (p.Phe31Cys) c.134T>G (p.Phe45Cys) c.137T>G (p.Phe46Cys) c.-209T>G (n.-209T>G) c.58T>G (p.Ser20Ala) | dbSNP |
| 8 | g.127738354T= | CA1818466271 | MYC | c.92T= (p.Phe31=) c.134T= (p.Phe45=) c.137T= (p.Phe46=) c.-209T= (n.-209T=) c.58T= (p.Ser20=) | |
| 8 | g.127738355C>A | CA372279418 | MYC | c.93C>A (p.Phe31Leu) c.135C>A (p.Phe45Leu) c.138C>A (p.Phe46Leu) c.-208C>A (n.-208C>A) c.59C>A (p.Ser20Tyr) | dbSNP |
| 8 | g.127738355C= | CA1818466274 | MYC | c.93C= (p.Phe31=) c.135C= (p.Phe45=) c.138C= (p.Phe46=) c.-208C= (n.-208C=) c.59C= (p.Ser20=) | |
| 8 | g.127738355C>G | CA372279420 | MYC | c.93C>G (p.Phe31Leu) c.135C>G (p.Phe45Leu) c.138C>G (p.Phe46Leu) c.-208C>G (n.-208C>G) c.59C>G (p.Ser20Cys) | |
| 8 | g.127738355C>T | CA372279419 | MYC | c.93C>T (p.Phe31=) c.135C>T (p.Phe45=) c.138C>T (p.Phe46=) c.-208C>T (n.-208C>T) c.59C>T (p.Ser20Phe) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.127738356_127738358del | CA2688552185 | MYC | c.94_96del (p.Tyr32del) c.136_138del (p.Tyr46del) c.139_141del (p.Tyr47del) c.-207_-205del (n.-207_-205del) c.60_62del (p.Thr21del) | gnomAD v4 |
| 8 | g.127738356T>A | CA372279421 | MYC | c.94T>A (p.Tyr32Asn) c.136T>A (p.Tyr46Asn) c.139T>A (p.Tyr47Asn) c.-207T>A (n.-207T>A) c.60T>A (p.Ser20=) | |
| 8 | g.127738356T>C | CA4875233 | MYC | c.94T>C (p.Tyr32His) c.136T>C (p.Tyr46His) c.139T>C (p.Tyr47His) c.-207T>C (n.-207T>C) c.60T>C (p.Ser20=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738356T>G | CA372279422 | MYC | c.94T>G (p.Tyr32Asp) c.136T>G (p.Tyr46Asp) c.139T>G (p.Tyr47Asp) c.-207T>G (n.-207T>G) c.60T>G (p.Ser20=) | |
| 8 | g.127738356T= | CA1818466277 | MYC | c.94T= (p.Tyr32=) c.136T= (p.Tyr46=) c.139T= (p.Tyr47=) c.-207T= (n.-207T=) c.60T= (p.Ser20=) | |
| 8 | g.127738357A= | CA1818466278 | MYC | c.95A= (p.Tyr32=) c.137A= (p.Tyr46=) c.140A= (p.Tyr47=) c.-206A= (n.-206A=) c.61A= (p.Thr21=) | |
| 8 | g.127738357A>C | CA372279423 | MYC | c.95A>C (p.Tyr32Ser) c.137A>C (p.Tyr46Ser) c.140A>C (p.Tyr47Ser) c.-206A>C (n.-206A>C) c.61A>C (p.Thr21Pro) | |
| 8 | g.127738357A>G | CA372279424 | MYC | c.95A>G (p.Tyr32Cys) c.137A>G (p.Tyr46Cys) c.140A>G (p.Tyr47Cys) c.-206A>G (n.-206A>G) c.61A>G (p.Thr21Ala) | dbSNP |
| 8 | g.127738357A>T | CA372279425 | MYC | c.95A>T (p.Tyr32Phe) c.137A>T (p.Tyr46Phe) c.140A>T (p.Tyr47Phe) c.-206A>T (n.-206A>T) c.61A>T (p.Thr21Ser) | dbSNP |
| 8 | g.127738358C>A | CA372279427 | MYC | c.96C>A (p.Tyr32Ter) c.138C>A (p.Tyr46Ter) c.141C>A (p.Tyr47Ter) c.-205C>A (n.-205C>A) c.62C>A (p.Thr21Asn) | |
| 8 | g.127738358C>G | CA372279428 | MYC | c.96C>G (p.Tyr32Ter) c.138C>G (p.Tyr46Ter) c.141C>G (p.Tyr47Ter) c.-205C>G (n.-205C>G) c.62C>G (p.Thr21Ser) | |
| 8 | g.127738358C>T | CA372279426 | MYC | c.96C>T (p.Tyr32=) c.138C>T (p.Tyr46=) c.141C>T (p.Tyr47=) c.-205C>T (n.-205C>T) c.62C>T (p.Thr21Ile) | gnomAD v4 |
| 8 | g.127738358_127738361delinsCCAG | CA1818466280 | MYC | c.96_99delinsCCAG (p.Tyr32=) c.138_141delinsCCAG (p.Tyr46=) c.141_144delinsCCAG (p.Tyr47=) c.-205_-202delinsCCAG (n.-205_-202delinsCCAG) c.62_65delinsCCAG (p.Thr21=) | |
| 8 | g.127738359C>A | CA372279429 | MYC | c.97C>A (p.Gln33Lys) c.139C>A (p.Gln47Lys) c.142C>A (p.Gln48Lys) c.-204C>A (n.-204C>A) c.63C>A (p.Thr21=) | dbSNP |
| 8 | g.127738359C>G | CA372279430 | MYC | c.97C>G (p.Gln33Glu) c.139C>G (p.Gln47Glu) c.142C>G (p.Gln48Glu) c.-204C>G (n.-204C>G) c.63C>G (p.Thr21=) | |
| 8 | g.127738359C>T | CA372279431 | MYC | c.97C>T (p.Gln33Ter) c.139C>T (p.Gln47Ter) c.142C>T (p.Gln48Ter) c.-204C>T (n.-204C>T) c.63C>T (p.Thr21=) | dbSNP |
| 8 | g.127738371_127738373dup | CA4875235 | MYC | c.109_111dup (p.Gln37_Ser38insGln) c.151_153dup (p.Gln51_Ser52insGln) c.154_156dup (p.Gln52_Ser53insGln) c.-192_-190dup (n.-192_-190dup) c.75_77dup (p.Ser25_Arg26insSer) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738371_127738373del | CA4875234 | MYC | c.109_111del (p.Gln37del) c.151_153del (p.Gln51del) c.154_156del (p.Gln52del) c.-192_-190del (n.-192_-190del) c.75_77del (p.Ser25del) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738360A>C | CA372279432 | MYC | c.98A>C (p.Gln33Pro) c.140A>C (p.Gln47Pro) c.143A>C (p.Gln48Pro) c.-203A>C (n.-203A>C) c.64A>C (p.Ser22Arg) | |
| 8 | g.127738360A>G | CA372279433 | MYC | c.98A>G (p.Gln33Arg) c.140A>G (p.Gln47Arg) c.143A>G (p.Gln48Arg) c.-203A>G (n.-203A>G) c.64A>G (p.Ser22Gly) | |
| 8 | g.127738360A>T | CA372279434 | MYC | c.98A>T (p.Gln33Leu) c.140A>T (p.Gln47Leu) c.143A>T (p.Gln48Leu) c.-203A>T (n.-203A>T) c.64A>T (p.Ser22Cys) | dbSNP |
| 8 | g.127738361G>A | CA4875237 | MYC | c.99G>A (p.Gln33=) c.141G>A (p.Gln47=) c.144G>A (p.Gln48=) c.-202G>A (n.-202G>A) c.65G>A (p.Ser22Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738361G>C | CA4875236 | MYC | c.99G>C (p.Gln33His) c.141G>C (p.Gln47His) c.144G>C (p.Gln48His) c.-202G>C (n.-202G>C) c.65G>C (p.Ser22Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738361G= | CA1818466300 | MYC | c.99G= (p.Gln33=) c.141G= (p.Gln47=) c.144G= (p.Gln48=) c.-202G= (n.-202G=) c.65G= (p.Ser22=) | |
| 8 | g.127738361G>T | CA372279435 | MYC | c.99G>T (p.Gln33His) c.141G>T (p.Gln47His) c.144G>T (p.Gln48His) c.-202G>T (n.-202G>T) c.65G>T (p.Ser22Ile) | |
| 8 | g.127738362C>A | CA372279436 | MYC | c.100C>A (p.Gln34Lys) c.142C>A (p.Gln48Lys) c.145C>A (p.Gln49Lys) c.-201C>A (n.-201C>A) c.66C>A (p.Ser22Arg) | dbSNP |
| 8 | g.127738362C>G | CA372279437 | MYC | c.100C>G (p.Gln34Glu) c.142C>G (p.Gln48Glu) c.145C>G (p.Gln49Glu) c.-201C>G (n.-201C>G) c.66C>G (p.Ser22Arg) | |
| 8 | g.127738362C>T | CA372279438 | MYC | c.100C>T (p.Gln34Ter) c.142C>T (p.Gln48Ter) c.145C>T (p.Gln49Ter) c.-201C>T (n.-201C>T) c.66C>T (p.Ser22=) | dbSNP |
| 8 | g.127738363A= | CA1818466303 | MYC | c.101A= (p.Gln34=) c.143A= (p.Gln48=) c.146A= (p.Gln49=) c.-200A= (n.-200A=) c.67A= (p.Ser23=) | |
| 8 | g.127738363A>C | CA372279440 | MYC | c.101A>C (p.Gln34Pro) c.143A>C (p.Gln48Pro) c.146A>C (p.Gln49Pro) c.-200A>C (n.-200A>C) c.67A>C (p.Ser23Arg) | |
| 8 | g.127738363A>G | CA185777060 | MYC | c.101A>G (p.Gln34Arg) c.143A>G (p.Gln48Arg) c.146A>G (p.Gln49Arg) c.-200A>G (n.-200A>G) c.67A>G (p.Ser23Gly) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738363A>T | CA372279439 | MYC | c.101A>T (p.Gln34Leu) c.143A>T (p.Gln48Leu) c.146A>T (p.Gln49Leu) c.-200A>T (n.-200A>T) c.67A>T (p.Ser23Cys) | dbSNP |
| 8 | g.127738363_127738364delinsTT | CA2573332251 | MYC | c.101_102delinsTT (p.Gln34Leu) c.143_144delinsTT (p.Gln48Leu) c.146_147delinsTT (p.Gln49Leu) c.-200_-199delinsTT (n.-200_-199delinsTT) c.67_68delinsTT (p.Ser23Phe) | |
| 8 | g.127738364G>A | CA372279441 | MYC | c.102G>A (p.Gln34=) c.144G>A (p.Gln48=) c.147G>A (p.Gln49=) c.-199G>A (n.-199G>A) c.68G>A (p.Ser23Asn) | dbSNP |
| 8 | g.127738364G>C | CA372279442 | MYC | c.102G>C (p.Gln34His) c.144G>C (p.Gln48His) c.147G>C (p.Gln49His) c.-199G>C (n.-199G>C) c.68G>C (p.Ser23Thr) | dbSNP COSMIC COSMIC |
| 8 | g.127738364G>T | CA372279443 | MYC | c.102G>T (p.Gln34His) c.144G>T (p.Gln48His) c.147G>T (p.Gln49His) c.-199G>T (n.-199G>T) c.68G>T (p.Ser23Ile) | |
| 8 | g.127738365C>A | CA372279444 | MYC | c.103C>A (p.Gln35Lys) c.145C>A (p.Gln49Lys) c.148C>A (p.Gln50Lys) c.-198C>A (n.-198C>A) c.69C>A (p.Ser23Arg) | dbSNP |
| 8 | g.127738365C>G | CA372279445 | MYC | c.103C>G (p.Gln35Glu) c.145C>G (p.Gln49Glu) c.148C>G (p.Gln50Glu) c.-198C>G (n.-198C>G) c.69C>G (p.Ser23Arg) | dbSNP |
| 8 | g.127738365C>T | CA372279446 | MYC | c.103C>T (p.Gln35Ter) c.145C>T (p.Gln49Ter) c.148C>T (p.Gln50Ter) c.-198C>T (n.-198C>T) c.69C>T (p.Ser23=) | dbSNP |
| 8 | g.127738366A>C | CA372279447 | MYC | c.104A>C (p.Gln35Pro) c.146A>C (p.Gln49Pro) c.149A>C (p.Gln50Pro) c.-197A>C (n.-197A>C) c.70A>C (p.Ser24Arg) | dbSNP |
| 8 | g.127738366A>G | CA372279448 | MYC | c.104A>G (p.Gln35Arg) c.146A>G (p.Gln49Arg) c.149A>G (p.Gln50Arg) c.-197A>G (n.-197A>G) c.70A>G (p.Ser24Gly) | dbSNP |
| 8 | g.127738366A>T | CA372279449 | MYC | c.104A>T (p.Gln35Leu) c.146A>T (p.Gln49Leu) c.149A>T (p.Gln50Leu) c.-197A>T (n.-197A>T) c.70A>T (p.Ser24Cys) | COSMIC COSMIC |
| 8 | g.127738367G>A | CA372279450 | MYC | c.105G>A (p.Gln35=) c.147G>A (p.Gln49=) c.150G>A (p.Gln50=) c.-196G>A (n.-196G>A) c.71G>A (p.Ser24Asn) | dbSNP COSMIC COSMIC |
| 8 | g.127738367G>C | CA372279451 | MYC | c.105G>C (p.Gln35His) c.147G>C (p.Gln49His) c.150G>C (p.Gln50His) c.-196G>C (n.-196G>C) c.71G>C (p.Ser24Thr) | |
| 8 | g.127738367G= | CA1818466310 | MYC | c.105G= (p.Gln35=) c.147G= (p.Gln49=) c.150G= (p.Gln50=) c.-196G= (n.-196G=) c.71G= (p.Ser24=) | |
| 8 | g.127738367G>T | CA185777061 | MYC | c.105G>T (p.Gln35His) c.147G>T (p.Gln49His) c.150G>T (p.Gln50His) c.-196G>T (n.-196G>T) c.71G>T (p.Ser24Ile) | dbSNP COSMIC COSMIC |
| 8 | g.127738368C>A | CA372279454 | MYC | c.106C>A (p.Gln36Lys) c.148C>A (p.Gln50Lys) c.151C>A (p.Gln51Lys) c.-195C>A (n.-195C>A) c.72C>A (p.Ser24Arg) | dbSNP |
| 8 | g.127738368C= | CA1818466314 | MYC | c.106C= (p.Gln36=) c.148C= (p.Gln50=) c.151C= (p.Gln51=) c.-195C= (n.-195C=) c.72C= (p.Ser24=) | |
| 8 | g.127738368C>G | CA372279453 | MYC | c.106C>G (p.Gln36Glu) c.148C>G (p.Gln50Glu) c.151C>G (p.Gln51Glu) c.-195C>G (n.-195C>G) c.72C>G (p.Ser24Arg) | dbSNP |
| 8 | g.127738368C>T | CA372279452 | MYC | c.106C>T (p.Gln36Ter) c.148C>T (p.Gln50Ter) c.151C>T (p.Gln51Ter) c.-195C>T (n.-195C>T) c.72C>T (p.Ser24=) | dbSNP |
| 8 | g.127738369A>C | CA372279457 | MYC | c.107A>C (p.Gln36Pro) c.149A>C (p.Gln50Pro) c.152A>C (p.Gln51Pro) c.-194A>C (n.-194A>C) c.73A>C (p.Ser25Arg) | |
| 8 | g.127738369A>G | CA372279455 | MYC | c.107A>G (p.Gln36Arg) c.149A>G (p.Gln50Arg) c.152A>G (p.Gln51Arg) c.-194A>G (n.-194A>G) c.73A>G (p.Ser25Gly) | dbSNP |
| 8 | g.127738369A>T | CA372279456 | MYC | c.107A>T (p.Gln36Leu) c.149A>T (p.Gln50Leu) c.152A>T (p.Gln51Leu) c.-194A>T (n.-194A>T) c.73A>T (p.Ser25Cys) | dbSNP |
| 8 | g.127738370G>A | CA372279458 | MYC | c.108G>A (p.Gln36=) c.150G>A (p.Gln50=) c.153G>A (p.Gln51=) c.-193G>A (n.-193G>A) c.74G>A (p.Ser25Asn) | dbSNP COSMIC COSMIC |
| 8 | g.127738370G>C | CA372279459 | MYC | c.108G>C (p.Gln36His) c.150G>C (p.Gln50His) c.153G>C (p.Gln51His) c.-193G>C (n.-193G>C) c.74G>C (p.Ser25Thr) | dbSNP |
| 8 | g.127738370G>T | CA372279460 | MYC | c.108G>T (p.Gln36His) c.150G>T (p.Gln50His) c.153G>T (p.Gln51His) c.-193G>T (n.-193G>T) c.74G>T (p.Ser25Ile) | |
| 8 | g.127738371C>A | CA372279463 | MYC | c.109C>A (p.Gln37Lys) c.151C>A (p.Gln51Lys) c.154C>A (p.Gln52Lys) c.-192C>A (n.-192C>A) c.75C>A (p.Ser25Arg) | dbSNP gnomAD v4 |
| 8 | g.127738371C= | CA1818466319 | MYC | c.109C= (p.Gln37=) c.151C= (p.Gln51=) c.154C= (p.Gln52=) c.-192C= (n.-192C=) c.75C= (p.Ser25=) | |
| 8 | g.127738371C>G | CA372279462 | MYC | c.109C>G (p.Gln37Glu) c.151C>G (p.Gln51Glu) c.154C>G (p.Gln52Glu) c.-192C>G (n.-192C>G) c.75C>G (p.Ser25Arg) | dbSNP |
| 8 | g.127738371C>T | CA372279461 | MYC | c.109C>T (p.Gln37Ter) c.151C>T (p.Gln51Ter) c.154C>T (p.Gln52Ter) c.-192C>T (n.-192C>T) c.75C>T (p.Ser25=) | dbSNP |
| 8 | g.127738372_127738373insTCA | CA2579248078 | MYC | c.110_111insTCA (p.Gln36_Gln37insHis) c.152_153insTCA (p.Gln50_Gln51insHis) c.155_156insTCA (p.Gln51_Gln52insHis) c.-191_-190insTCA (n.-191_-190insTCA) c.76_77insTCA (p.Ser25_Arg26insIle) | |
| 8 | g.127738372A= | CA1818466322 | MYC | c.110A= (p.Gln37=) c.152A= (p.Gln51=) c.155A= (p.Gln52=) c.-191A= (n.-191A=) c.76A= (p.Arg26=) | |
| 8 | g.127738372A>C | CA372279464 | MYC | c.110A>C (p.Gln37Pro) c.152A>C (p.Gln51Pro) c.155A>C (p.Gln52Pro) c.-191A>C (n.-191A>C) c.76A>C (p.Arg26=) | |
| 8 | g.127738372A>G | CA372279465 | MYC | c.110A>G (p.Gln37Arg) c.152A>G (p.Gln51Arg) c.155A>G (p.Gln52Arg) c.-191A>G (n.-191A>G) c.76A>G (p.Arg26Gly) | dbSNP |
| 8 | g.127738372A>T | CA372279466 | MYC | c.110A>T (p.Gln37Leu) c.152A>T (p.Gln51Leu) c.155A>T (p.Gln52Leu) c.-191A>T (n.-191A>T) c.76A>T (p.Arg26Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738373G>A | CA4875238 | MYC | c.111G>A (p.Gln37=) c.153G>A (p.Gln51=) c.156G>A (p.Gln52=) c.-190G>A (n.-190G>A) c.77G>A (p.Arg26Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738373G>C | CA372279467 | MYC | c.111G>C (p.Gln37His) c.153G>C (p.Gln51His) c.156G>C (p.Gln52His) c.-190G>C (n.-190G>C) c.77G>C (p.Arg26Thr) | COSMIC COSMIC |
| 8 | g.127738373G= | CA1818466328 | MYC | c.111G= (p.Gln37=) c.153G= (p.Gln51=) c.156G= (p.Gln52=) c.-190G= (n.-190G=) c.77G= (p.Arg26=) | |
| 8 | g.127738373G>T | CA372279468 | MYC | c.111G>T (p.Gln37His) c.153G>T (p.Gln51His) c.156G>T (p.Gln52His) c.-190G>T (n.-190G>T) c.77G>T (p.Arg26Ile) | dbSNP |
| 8 | g.127738374A>C | CA372279469 | MYC | c.112A>C (p.Ser38Arg) c.154A>C (p.Ser52Arg) c.157A>C (p.Ser53Arg) c.-189A>C (n.-189A>C) c.78A>C (p.Arg26Ser) | |
| 8 | g.127738374A>G | CA372279471 | MYC | c.112A>G (p.Ser38Gly) c.154A>G (p.Ser52Gly) c.157A>G (p.Ser53Gly) c.-189A>G (n.-189A>G) c.78A>G (p.Arg26=) | dbSNP |
| 8 | g.127738374A>T | CA372279470 | MYC | c.112A>T (p.Ser38Cys) c.154A>T (p.Ser52Cys) c.157A>T (p.Ser53Cys) c.-189A>T (n.-189A>T) c.78A>T (p.Arg26Ser) | dbSNP |
| 8 | g.127738375G>A | CA372279472 | MYC | c.113G>A (p.Ser38Asn) c.155G>A (p.Ser52Asn) c.158G>A (p.Ser53Asn) c.-188G>A (n.-188G>A) c.79G>A (p.Ala27Thr) | dbSNP |
| 8 | g.127738375G>C | CA372279473 | MYC | c.113G>C (p.Ser38Thr) c.155G>C (p.Ser52Thr) c.158G>C (p.Ser53Thr) c.-188G>C (n.-188G>C) c.79G>C (p.Ala27Pro) | |
| 8 | g.127738375G>T | CA372279474 | MYC | c.113G>T (p.Ser38Ile) c.155G>T (p.Ser52Ile) c.158G>T (p.Ser53Ile) c.-188G>T (n.-188G>T) c.79G>T (p.Ala27Ser) | |
| 8 | g.127738376C>A | CA372279475 | MYC | c.114C>A (p.Ser38Arg) c.156C>A (p.Ser52Arg) c.159C>A (p.Ser53Arg) c.-187C>A (n.-187C>A) c.80C>A (p.Ala27Glu) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.127738376C= | CA1818466330 | MYC | c.114C= (p.Ser38=) c.156C= (p.Ser52=) c.159C= (p.Ser53=) c.-187C= (n.-187C=) c.80C= (p.Ala27=) | |
| 8 | g.127738376C>G | CA372279476 | MYC | c.114C>G (p.Ser38Arg) c.156C>G (p.Ser52Arg) c.159C>G (p.Ser53Arg) c.-187C>G (n.-187C>G) c.80C>G (p.Ala27Gly) | dbSNP |
| 8 | g.127738376C>T | CA372279477 | MYC | c.114C>T (p.Ser38=) c.156C>T (p.Ser52=) c.159C>T (p.Ser53=) c.-187C>T (n.-187C>T) c.80C>T (p.Ala27Val) | dbSNP |
| 8 | g.127738377G>A | CA372279478 | MYC | c.115G>A (p.Glu39Lys) c.157G>A (p.Glu53Lys) c.160G>A (p.Glu54Lys) c.-186G>A (n.-186G>A) c.81G>A (p.Ala27=) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.127738377G>C | CA4875239 | MYC | c.115G>C (p.Glu39Gln) c.157G>C (p.Glu53Gln) c.160G>C (p.Glu54Gln) c.-186G>C (n.-186G>C) c.81G>C (p.Ala27=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738377G= | CA1818466333 | MYC | c.115G= (p.Glu39=) c.157G= (p.Glu53=) c.160G= (p.Glu54=) c.-186G= (n.-186G=) c.81G= (p.Ala27=) | |
| 8 | g.127738377G>T | CA372279479 | MYC | c.115G>T (p.Glu39Ter) c.157G>T (p.Glu53Ter) c.160G>T (p.Glu54Ter) c.-186G>T (n.-186G>T) c.81G>T (p.Ala27=) | dbSNP |
| 8 | g.127738378A>C | CA372279480 | MYC | c.116A>C (p.Glu39Ala) c.158A>C (p.Glu53Ala) c.161A>C (p.Glu54Ala) c.-185A>C (n.-185A>C) c.82A>C (p.Ser28Arg) | |
| 8 | g.127738378A>G | CA372279481 | MYC | c.116A>G (p.Glu39Gly) c.158A>G (p.Glu53Gly) c.161A>G (p.Glu54Gly) c.-185A>G (n.-185A>G) c.82A>G (p.Ser28Gly) | |
| 8 | g.127738378A>T | CA372279482 | MYC | c.116A>T (p.Glu39Val) c.158A>T (p.Glu53Val) c.161A>T (p.Glu54Val) c.-185A>T (n.-185A>T) c.82A>T (p.Ser28Cys) | |
| 8 | g.127738379G>A | CA372279484 | MYC | c.117G>A (p.Glu39=) c.159G>A (p.Glu53=) c.162G>A (p.Glu54=) c.-184G>A (n.-184G>A) c.83G>A (p.Ser28Asn) | dbSNP COSMIC COSMIC |
| 8 | g.127738379G>C | CA122524 | MYC | c.117G>C (p.Glu39Asp) c.159G>C (p.Glu53Asp) c.162G>C (p.Glu54Asp) c.-184G>C (n.-184G>C) c.83G>C (p.Ser28Thr) | ClinVar dbSNP COSMIC COSMIC |
| 8 | g.127738379G= | CA1818466341 | MYC | c.117G= (p.Glu39=) c.159G= (p.Glu53=) c.162G= (p.Glu54=) c.-184G= (n.-184G=) c.83G= (p.Ser28=) | |
| 8 | g.127738379G>T | CA372279483 | MYC | c.117G>T (p.Glu39Asp) c.159G>T (p.Glu53Asp) c.162G>T (p.Glu54Asp) c.-184G>T (n.-184G>T) c.83G>T (p.Ser28Ile) | COSMIC COSMIC |
| 8 | g.127738380C>A | CA372279485 | MYC | c.118C>A (p.Leu40Met) c.160C>A (p.Leu54Met) c.163C>A (p.Leu55Met) c.-183C>A (n.-183C>A) c.84C>A (p.Ser28Arg) | dbSNP COSMIC COSMIC |
| 8 | g.127738380C= | CA1818466348 | MYC | c.118C= (p.Leu40=) c.160C= (p.Leu54=) c.163C= (p.Leu55=) c.-183C= (n.-183C=) c.84C= (p.Ser28=) | |
| 8 | g.127738380C>G | CA372279486 | MYC | c.118C>G (p.Leu40Val) c.160C>G (p.Leu54Val) c.163C>G (p.Leu55Val) c.-183C>G (n.-183C>G) c.84C>G (p.Ser28Arg) | gnomAD v4 |
| 8 | g.127738380C>T | CA4875240 | MYC | c.118C>T (p.Leu40=) c.160C>T (p.Leu54=) c.163C>T (p.Leu55=) c.-183C>T (n.-183C>T) c.84C>T (p.Ser28=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738381T>A | CA372279487 | MYC | c.119T>A (p.Leu40Gln) c.161T>A (p.Leu54Gln) c.164T>A (p.Leu55Gln) c.-182T>A (n.-182T>A) c.85T>A (p.Cys29Ser) | dbSNP |
| 8 | g.127738381T>C | CA372279488 | MYC | c.119T>C (p.Leu40Pro) c.161T>C (p.Leu54Pro) c.164T>C (p.Leu55Pro) c.-182T>C (n.-182T>C) c.85T>C (p.Cys29Arg) | dbSNP gnomAD v2 |
| 8 | g.127738381T>G | CA372279489 | MYC | c.119T>G (p.Leu40Arg) c.161T>G (p.Leu54Arg) c.164T>G (p.Leu55Arg) c.-182T>G (n.-182T>G) c.85T>G (p.Cys29Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.127738381T= | CA1818466352 | MYC | c.119T= (p.Leu40=) c.161T= (p.Leu54=) c.164T= (p.Leu55=) c.-182T= (n.-182T=) c.85T= (p.Cys29=) | |
| 8 | g.127738382G>A | CA372279491 | MYC | c.120G>A (p.Leu40=) c.162G>A (p.Leu54=) c.165G>A (p.Leu55=) c.-181G>A (n.-181G>A) c.86G>A (p.Cys29Tyr) | dbSNP gnomAD v4 |
| 8 | g.127738382G>C | CA372279490 | MYC | c.120G>C (p.Leu40=) c.162G>C (p.Leu54=) c.165G>C (p.Leu55=) c.-181G>C (n.-181G>C) c.86G>C (p.Cys29Ser) | dbSNP |
| 8 | g.127738382G= | CA1818466355 | MYC | c.120G= (p.Leu40=) c.162G= (p.Leu54=) c.165G= (p.Leu55=) c.-181G= (n.-181G=) c.86G= (p.Cys29=) | |
| 8 | g.127738382G>T | CA4875241 | MYC | c.120G>T (p.Leu40=) c.162G>T (p.Leu54=) c.165G>T (p.Leu55=) c.-181G>T (n.-181G>T) c.86G>T (p.Cys29Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738383C>A | CA372279492 | MYC | c.121C>A (p.Gln41Lys) c.163C>A (p.Gln55Lys) c.166C>A (p.Gln56Lys) c.-180C>A (n.-180C>A) c.87C>A (p.Cys29Ter) | |
| 8 | g.127738383C>G | CA372279493 | MYC | c.121C>G (p.Gln41Glu) c.163C>G (p.Gln55Glu) c.166C>G (p.Gln56Glu) c.-180C>G (n.-180C>G) c.87C>G (p.Cys29Trp) | dbSNP |
| 8 | g.127738383C>T | CA372279494 | MYC | c.121C>T (p.Gln41Ter) c.163C>T (p.Gln55Ter) c.166C>T (p.Gln56Ter) c.-180C>T (n.-180C>T) c.87C>T (p.Cys29=) | dbSNP |
| 8 | g.127738384A>C | CA372279495 | MYC | c.122A>C (p.Gln41Pro) c.164A>C (p.Gln55Pro) c.167A>C (p.Gln56Pro) c.-179A>C (n.-179A>C) c.88A>C (p.Ser30Arg) | dbSNP |
| 8 | g.127738384A>G | CA372279496 | MYC | c.122A>G (p.Gln41Arg) c.164A>G (p.Gln55Arg) c.167A>G (p.Gln56Arg) c.-179A>G (n.-179A>G) c.88A>G (p.Ser30Gly) | dbSNP |
| 8 | g.127738384A>T | CA372279497 | MYC | c.122A>T (p.Gln41Leu) c.164A>T (p.Gln55Leu) c.167A>T (p.Gln56Leu) c.-179A>T (n.-179A>T) c.88A>T (p.Ser30Cys) | dbSNP |
| 8 | g.127738385G>A | CA372279498 | MYC | c.123G>A (p.Gln41=) c.165G>A (p.Gln55=) c.168G>A (p.Gln56=) c.-178G>A (n.-178G>A) c.89G>A (p.Ser30Asn) | gnomAD v4 |
| 8 | g.127738385G>C | CA372279500 | MYC | c.123G>C (p.Gln41His) c.165G>C (p.Gln55His) c.168G>C (p.Gln56His) c.-178G>C (n.-178G>C) c.89G>C (p.Ser30Thr) | dbSNP |
| 8 | g.127738385G>T | CA372279499 | MYC | c.123G>T (p.Gln41His) c.165G>T (p.Gln55His) c.168G>T (p.Gln56His) c.-178G>T (n.-178G>T) c.89G>T (p.Ser30Ile) | |
| 8 | g.127738386C>A | CA372279501 | MYC | c.124C>A (p.Pro42Thr) c.166C>A (p.Pro56Thr) c.169C>A (p.Pro57Thr) c.-177C>A (n.-177C>A) c.90C>A (p.Ser30Arg) | gnomAD v4 |
| 8 | g.127738386C= | CA1818466365 | MYC | c.124C= (p.Pro42=) c.166C= (p.Pro56=) c.169C= (p.Pro57=) c.-177C= (n.-177C=) c.90C= (p.Ser30=) | |
| 8 | g.127738386C>G | CA372279502 | MYC | c.124C>G (p.Pro42Ala) c.166C>G (p.Pro56Ala) c.169C>G (p.Pro57Ala) c.-177C>G (n.-177C>G) c.90C>G (p.Ser30Arg) | dbSNP |
| 8 | g.127738386C>T | CA16602745 | MYC | c.124C>T (p.Pro42Ser) c.166C>T (p.Pro56Ser) c.169C>T (p.Pro57Ser) c.-177C>T (n.-177C>T) c.90C>T (p.Ser30=) | ClinVar dbSNP gnomAD v4 |
| 8 | g.127738390del | CA2688552186 | MYC | c.128del (p.Pro43ArgfsTer?) c.170del (p.Pro57ArgfsTer?) c.173del (p.Pro58ArgfsTer?) c.-173del (n.-173del) c.94del (p.Arg32GlyfsTer21) | gnomAD v4 |
| 8 | g.127738387C>A | CA372279503 | MYC | c.125C>A (p.Pro42His) c.167C>A (p.Pro56His) c.170C>A (p.Pro57His) c.-176C>A (n.-176C>A) c.91C>A (p.Pro31Thr) | dbSNP |
| 8 | g.127738387C= | CA1818466370 | MYC | c.125C= (p.Pro42=) c.167C= (p.Pro56=) c.170C= (p.Pro57=) c.-176C= (n.-176C=) c.91C= (p.Pro31=) | |
| 8 | g.127738387C>G | CA372279504 | MYC | c.125C>G (p.Pro42Arg) c.167C>G (p.Pro56Arg) c.170C>G (p.Pro57Arg) c.-176C>G (n.-176C>G) c.91C>G (p.Pro31Ala) | |
| 8 | g.127738387C>T | CA185777062 | MYC | c.125C>T (p.Pro42Leu) c.167C>T (p.Pro56Leu) c.170C>T (p.Pro57Leu) c.-176C>T (n.-176C>T) c.91C>T (p.Pro31Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.127738388C>A | CA372279505 | MYC | c.126C>A (p.Pro42=) c.168C>A (p.Pro56=) c.171C>A (p.Pro57=) c.-175C>A (n.-175C>A) c.92C>A (p.Pro31His) | |
| 8 | g.127738388C= | CA1818466374 | MYC | c.126C= (p.Pro42=) c.168C= (p.Pro56=) c.171C= (p.Pro57=) c.-175C= (n.-175C=) c.92C= (p.Pro31=) | |
| 8 | g.127738388C>G | CA372279506 | MYC | c.126C>G (p.Pro42=) c.168C>G (p.Pro56=) c.171C>G (p.Pro57=) c.-175C>G (n.-175C>G) c.92C>G (p.Pro31Arg) | |
| 8 | g.127738388C>T | CA4875242 | MYC | c.126C>T (p.Pro42=) c.168C>T (p.Pro56=) c.171C>T (p.Pro57=) c.-175C>T (n.-175C>T) c.92C>T (p.Pro31Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738389C>A | CA372279507 | MYC | c.127C>A (p.Pro43Thr) c.169C>A (p.Pro57Thr) c.172C>A (p.Pro58Thr) c.-174C>A (n.-174C>A) c.93C>A (p.Pro31=) | |
| 8 | g.127738389C>G | CA372279508 | MYC | c.127C>G (p.Pro43Ala) c.169C>G (p.Pro57Ala) c.172C>G (p.Pro58Ala) c.-174C>G (n.-174C>G) c.93C>G (p.Pro31=) | gnomAD v4 |
| 8 | g.127738389C>T | CA372279509 | MYC | c.127C>T (p.Pro43Ser) c.169C>T (p.Pro57Ser) c.172C>T (p.Pro58Ser) c.-174C>T (n.-174C>T) c.93C>T (p.Pro31=) | dbSNP gnomAD v4 COSMIC COSMIC |
| 8 | g.127738390C>A | CA372279510 | MYC | c.128C>A (p.Pro43Gln) c.170C>A (p.Pro57Gln) c.173C>A (p.Pro58Gln) c.-173C>A (n.-173C>A) c.94C>A (p.Arg32=) | |
| 8 | g.127738390C= | CA1818466379 | MYC | c.128C= (p.Pro43=) c.170C= (p.Pro57=) c.173C= (p.Pro58=) c.-173C= (n.-173C=) c.94C= (p.Arg32=) | |
| 8 | g.127738390C>G | CA372279511 | MYC | c.128C>G (p.Pro43Arg) c.170C>G (p.Pro57Arg) c.173C>G (p.Pro58Arg) c.-173C>G (n.-173C>G) c.94C>G (p.Arg32Gly) | dbSNP |
| 8 | g.127738390C>T | CA16602893 | MYC | c.128C>T (p.Pro43Leu) c.170C>T (p.Pro57Leu) c.173C>T (p.Pro58Leu) c.-173C>T (n.-173C>T) c.94C>T (p.Arg32Trp) | ClinVar dbSNP |
| 8 | g.127738391G>A | CA372279512 | MYC | c.129G>A (p.Pro43=) c.171G>A (p.Pro57=) c.174G>A (p.Pro58=) c.-172G>A (n.-172G>A) c.95G>A (p.Arg32Gln) | dbSNP |
| 8 | g.127738391G>C | CA372279513 | MYC | c.129G>C (p.Pro43=) c.171G>C (p.Pro57=) c.174G>C (p.Pro58=) c.-172G>C (n.-172G>C) c.95G>C (p.Arg32Pro) | dbSNP |
| 8 | g.127738391G>T | CA372279514 | MYC | c.129G>T (p.Pro43=) c.171G>T (p.Pro57=) c.174G>T (p.Pro58=) c.-172G>T (n.-172G>T) c.95G>T (p.Arg32Leu) | gnomAD v4 |
| 8 | g.127738392G>A | CA372279515 | MYC | c.130G>A (p.Ala44Thr) c.172G>A (p.Ala58Thr) c.175G>A (p.Ala59Thr) c.-171G>A (n.-171G>A) c.96G>A (p.Arg32=) | dbSNP gnomAD v4 COSMIC COSMIC |
| 8 | g.127738392G>C | CA372279516 | MYC | c.130G>C (p.Ala44Pro) c.172G>C (p.Ala58Pro) c.175G>C (p.Ala59Pro) c.-171G>C (n.-171G>C) c.96G>C (p.Arg32=) | dbSNP |
| 8 | g.127738392G>T | CA372279517 | MYC | c.130G>T (p.Ala44Ser) c.172G>T (p.Ala58Ser) c.175G>T (p.Ala59Ser) c.-171G>T (n.-171G>T) c.96G>T (p.Arg32=) | dbSNP |
| 8 | g.127738393C>A | CA372279518 | MYC | c.131C>A (p.Ala44Glu) c.173C>A (p.Ala58Glu) c.176C>A (p.Ala59Glu) c.-170C>A (n.-170C>A) c.97C>A (p.Arg33Ser) | dbSNP gnomAD v4 |
| 8 | g.127738393C= | CA1818466383 | MYC | c.131C= (p.Ala44=) c.173C= (p.Ala58=) c.176C= (p.Ala59=) c.-170C= (n.-170C=) c.97C= (p.Arg33=) | |
| 8 | g.127738393C>G | CA372279519 | MYC | c.131C>G (p.Ala44Gly) c.173C>G (p.Ala58Gly) c.176C>G (p.Ala59Gly) c.-170C>G (n.-170C>G) c.97C>G (p.Arg33Gly) | dbSNP |
| 8 | g.127738393C>T | CA4875243 | MYC | c.131C>T (p.Ala44Val) c.173C>T (p.Ala58Val) c.176C>T (p.Ala59Val) c.-170C>T (n.-170C>T) c.97C>T (p.Arg33Cys) | ClinVar dbSNP ExAC gnomAD v2 COSMIC COSMIC |
| 8 | g.127738394G>A | CA372279520 | MYC | c.132G>A (p.Ala44=) c.174G>A (p.Ala58=) c.177G>A (p.Ala59=) c.-169G>A (n.-169G>A) c.98G>A (p.Arg33His) | dbSNP gnomAD v2 |
| 8 | g.127738394G>C | CA372279521 | MYC | c.132G>C (p.Ala44=) c.174G>C (p.Ala58=) c.177G>C (p.Ala59=) c.-169G>C (n.-169G>C) c.98G>C (p.Arg33Pro) | |
| 8 | g.127738394G= | CA1818466388 | MYC | c.132G= (p.Ala44=) c.174G= (p.Ala58=) c.177G= (p.Ala59=) c.-169G= (n.-169G=) c.98G= (p.Arg33=) | |
| 8 | g.127738394G>T | CA4875244 | MYC | c.132G>T (p.Ala44=) c.174G>T (p.Ala58=) c.177G>T (p.Ala59=) c.-169G>T (n.-169G>T) c.98G>T (p.Arg33Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738395C>A | CA372279524 | MYC | c.133C>A (p.Pro45Thr) c.175C>A (p.Pro59Thr) c.178C>A (p.Pro60Thr) c.-168C>A (n.-168C>A) c.99C>A (p.Arg33=) | dbSNP |
| 8 | g.127738395C>G | CA372279522 | MYC | c.133C>G (p.Pro45Ala) c.175C>G (p.Pro59Ala) c.178C>G (p.Pro60Ala) c.-168C>G (n.-168C>G) c.99C>G (p.Arg33=) | |
| 8 | g.127738395C>T | CA372279523 | MYC | c.133C>T (p.Pro45Ser) c.175C>T (p.Pro59Ser) c.178C>T (p.Pro60Ser) c.-168C>T (n.-168C>T) c.99C>T (p.Arg33=) | dbSNP |
| 8 | g.127738396C>A | CA372279525 | MYC | c.134C>A (p.Pro45His) c.176C>A (p.Pro59His) c.179C>A (p.Pro60His) c.-167C>A (n.-167C>A) c.100C>A (p.Pro34Thr) | dbSNP |
| 8 | g.127738396C>G | CA372279526 | MYC | c.134C>G (p.Pro45Arg) c.176C>G (p.Pro59Arg) c.179C>G (p.Pro60Arg) c.-167C>G (n.-167C>G) c.100C>G (p.Pro34Ala) | dbSNP |
| 8 | g.127738396C>T | CA372279527 | MYC | c.134C>T (p.Pro45Leu) c.176C>T (p.Pro59Leu) c.179C>T (p.Pro60Leu) c.-167C>T (n.-167C>T) c.100C>T (p.Pro34Ser) | dbSNP |
| 8 | g.127738397C>A | CA372279528 | MYC | c.135C>A (p.Pro45=) c.177C>A (p.Pro59=) c.180C>A (p.Pro60=) c.-166C>A (n.-166C>A) c.101C>A (p.Pro34Gln) | |
| 8 | g.127738397C>G | CA372279529 | MYC | c.135C>G (p.Pro45=) c.177C>G (p.Pro59=) c.180C>G (p.Pro60=) c.-166C>G (n.-166C>G) c.101C>G (p.Pro34Arg) | dbSNP |
| 8 | g.127738397C>T | CA372279530 | MYC | c.135C>T (p.Pro45=) c.177C>T (p.Pro59=) c.180C>T (p.Pro60=) c.-166C>T (n.-166C>T) c.101C>T (p.Pro34Leu) | dbSNP gnomAD v4 |
| 8 | g.127738398A>C | CA372279531 | MYC | c.136A>C (p.Ser46Arg) c.178A>C (p.Ser60Arg) c.181A>C (p.Ser61Arg) c.-165A>C (n.-165A>C) c.102A>C (p.Pro34=) | |
| 8 | g.127738398A>G | CA372279532 | MYC | c.136A>G (p.Ser46Gly) c.178A>G (p.Ser60Gly) c.181A>G (p.Ser61Gly) c.-165A>G (n.-165A>G) c.102A>G (p.Pro34=) | dbSNP |
| 8 | g.127738398A>T | CA372279533 | MYC | c.136A>T (p.Ser46Cys) c.178A>T (p.Ser60Cys) c.181A>T (p.Ser61Cys) c.-165A>T (n.-165A>T) c.102A>T (p.Pro34=) | dbSNP |
| 8 | g.127738399G>A | CA372279534 | MYC | c.137G>A (p.Ser46Asn) c.179G>A (p.Ser60Asn) c.182G>A (p.Ser61Asn) c.-164G>A (n.-164G>A) c.103G>A (p.Ala35Thr) | gnomAD v4 |
| 8 | g.127738399G>C | CA372279535 | MYC | c.137G>C (p.Ser46Thr) c.179G>C (p.Ser60Thr) c.182G>C (p.Ser61Thr) c.-164G>C (n.-164G>C) c.103G>C (p.Ala35Pro) | dbSNP |
| 8 | g.127738399G>T | CA372279536 | MYC | c.137G>T (p.Ser46Ile) c.179G>T (p.Ser60Ile) c.182G>T (p.Ser61Ile) c.-164G>T (n.-164G>T) c.103G>T (p.Ala35Ser) | |
| 8 | g.127738400C>A | CA372279537 | MYC | c.138C>A (p.Ser46Arg) c.180C>A (p.Ser60Arg) c.183C>A (p.Ser61Arg) c.-163C>A (n.-163C>A) c.104C>A (p.Ala35Glu) | dbSNP |
| 8 | g.127738400C= | CA1818466392 | MYC | c.138C= (p.Ser46=) c.180C= (p.Ser60=) c.183C= (p.Ser61=) c.-163C= (n.-163C=) c.104C= (p.Ala35=) | |
| 8 | g.127738400C>G | CA372279538 | MYC | c.138C>G (p.Ser46Arg) c.180C>G (p.Ser60Arg) c.183C>G (p.Ser61Arg) c.-163C>G (n.-163C>G) c.104C>G (p.Ala35Gly) | dbSNP |
| 8 | g.127738400C>T | CA4875245 | MYC | c.138C>T (p.Ser46=) c.180C>T (p.Ser60=) c.183C>T (p.Ser61=) c.-163C>T (n.-163C>T) c.104C>T (p.Ala35Val) | dbSNP ExAC gnomAD v2 |
| 8 | g.127738401G>A | CA372279540 | MYC | c.139G>A (p.Glu47Lys) c.181G>A (p.Glu61Lys) c.184G>A (p.Glu62Lys) c.-162G>A (n.-162G>A) c.105G>A (p.Ala35=) | dbSNP |
| 8 | g.127738401G>C | CA372279539 | MYC | c.139G>C (p.Glu47Gln) c.181G>C (p.Glu61Gln) c.184G>C (p.Glu62Gln) c.-162G>C (n.-162G>C) c.105G>C (p.Ala35=) | dbSNP |
| 8 | g.127738401G>T | CA372279541 | MYC | c.139G>T (p.Glu47Ter) c.181G>T (p.Glu61Ter) c.184G>T (p.Glu62Ter) c.-162G>T (n.-162G>T) c.105G>T (p.Ala35=) | |
| 8 | g.127738402A>C | CA372279542 | MYC | c.140A>C (p.Glu47Ala) c.182A>C (p.Glu61Ala) c.185A>C (p.Glu62Ala) c.-161A>C (n.-161A>C) c.106A>C (p.Arg36=) | |
| 8 | g.127738402A>G | CA372279543 | MYC | c.140A>G (p.Glu47Gly) c.182A>G (p.Glu61Gly) c.185A>G (p.Glu62Gly) c.-161A>G (n.-161A>G) c.106A>G (p.Arg36Gly) | dbSNP |
| 8 | g.127738402A>T | CA372279544 | MYC | c.140A>T (p.Glu47Val) c.182A>T (p.Glu61Val) c.185A>T (p.Glu62Val) c.-161A>T (n.-161A>T) c.106A>T (p.Arg36Trp) | dbSNP |
| 8 | g.127738403G>A | CA372279545 | MYC | c.141G>A (p.Glu47=) c.183G>A (p.Glu61=) c.186G>A (p.Glu62=) c.-160G>A (n.-160G>A) c.107G>A (p.Arg36Lys) | dbSNP |
| 8 | g.127738403G>C | CA372279546 | MYC | c.141G>C (p.Glu47Asp) c.183G>C (p.Glu61Asp) c.186G>C (p.Glu62Asp) c.-160G>C (n.-160G>C) c.107G>C (p.Arg36Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738403G= | CA1818466397 | MYC | c.141G= (p.Glu47=) c.183G= (p.Glu61=) c.186G= (p.Glu62=) c.-160G= (n.-160G=) c.107G= (p.Arg36=) | |
| 8 | g.127738403G>T | CA372279547 | MYC | c.141G>T (p.Glu47Asp) c.183G>T (p.Glu61Asp) c.186G>T (p.Glu62Asp) c.-160G>T (n.-160G>T) c.107G>T (p.Arg36Met) | |
| 8 | g.127738404G>A | CA372279548 | MYC | c.142G>A (p.Asp48Asn) c.184G>A (p.Asp62Asn) c.187G>A (p.Asp63Asn) c.-159G>A (n.-159G>A) c.108G>A (p.Arg36=) | dbSNP gnomAD v4 |
| 8 | g.127738404G>C | CA372279549 | MYC | c.142G>C (p.Asp48His) c.184G>C (p.Asp62His) c.187G>C (p.Asp63His) c.-159G>C (n.-159G>C) c.108G>C (p.Arg36Ser) | dbSNP |
| 8 | g.127738404G>T | CA372279550 | MYC | c.142G>T (p.Asp48Tyr) c.184G>T (p.Asp62Tyr) c.187G>T (p.Asp63Tyr) c.-159G>T (n.-159G>T) c.108G>T (p.Arg36Ser) | dbSNP |
| 8 | g.127738405A= | CA1818466399 | MYC | c.143A= (p.Asp48=) c.185A= (p.Asp62=) c.188A= (p.Asp63=) c.-158A= (n.-158A=) c.109A= (p.Ile37=) | |
| 8 | g.127738405A>C | CA4875246 | MYC | c.143A>C (p.Asp48Ala) c.185A>C (p.Asp62Ala) c.188A>C (p.Asp63Ala) c.-158A>C (n.-158A>C) c.109A>C (p.Ile37Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738405A>G | CA372279551 | MYC | c.143A>G (p.Asp48Gly) c.185A>G (p.Asp62Gly) c.188A>G (p.Asp63Gly) c.-158A>G (n.-158A>G) c.109A>G (p.Ile37Val) | dbSNP |
| 8 | g.127738405A>T | CA372279552 | MYC | c.143A>T (p.Asp48Val) c.185A>T (p.Asp62Val) c.188A>T (p.Asp63Val) c.-158A>T (n.-158A>T) c.109A>T (p.Ile37Leu) | |
| 8 | g.127738406T>A | CA372279555 | MYC | c.144T>A (p.Asp48Glu) c.186T>A (p.Asp62Glu) c.189T>A (p.Asp63Glu) c.-157T>A (n.-157T>A) c.110T>A (p.Ile37Lys) | dbSNP |
| 8 | g.127738406T>C | CA372279553 | MYC | c.144T>C (p.Asp48=) c.186T>C (p.Asp62=) c.189T>C (p.Asp63=) c.-157T>C (n.-157T>C) c.110T>C (p.Ile37Thr) | |
| 8 | g.127738406T>G | CA372279554 | MYC | c.144T>G (p.Asp48Glu) c.186T>G (p.Asp62Glu) c.189T>G (p.Asp63Glu) c.-157T>G (n.-157T>G) c.110T>G (p.Ile37Arg) | dbSNP |
| 8 | g.127738407A>C | CA372279556 | MYC | c.145A>C (p.Ile49Leu) c.187A>C (p.Ile63Leu) c.190A>C (p.Ile64Leu) c.-156A>C (n.-156A>C) c.111A>C (p.Ile37=) | |
| 8 | g.127738407A>G | CA372279557 | MYC | c.145A>G (p.Ile49Val) c.187A>G (p.Ile63Val) c.190A>G (p.Ile64Val) c.-156A>G (n.-156A>G) c.111A>G (p.Ile37Met) | COSMIC COSMIC |
| 8 | g.127738407A>T | CA372279558 | MYC | c.145A>T (p.Ile49Phe) c.187A>T (p.Ile63Phe) c.190A>T (p.Ile64Phe) c.-156A>T (n.-156A>T) c.111A>T (p.Ile37=) | |
| 8 | g.127738407_127738520del | CA645565236 | MYC | c.145_258del (p.Ile49_Asn86del) c.187_300del (p.Ile63_Asn100del) c.190_303del (p.Ile64_Asn101del) c.-156_-43del (n.-156_-43del) | COSMIC COSMIC |
| 8 | g.127738408T>A | CA372279559 | MYC | c.146T>A (p.Ile49Asn) c.188T>A (p.Ile63Asn) c.191T>A (p.Ile64Asn) c.-155T>A (n.-155T>A) c.112T>A (p.Ser38Thr) | |
| 8 | g.127738408T>C | CA372279560 | MYC | c.146T>C (p.Ile49Thr) c.188T>C (p.Ile63Thr) c.191T>C (p.Ile64Thr) c.-155T>C (n.-155T>C) c.112T>C (p.Ser38Pro) | gnomAD v4 |
| 8 | g.127738408T>G | CA372279561 | MYC | c.146T>G (p.Ile49Ser) c.188T>G (p.Ile63Ser) c.191T>G (p.Ile64Ser) c.-155T>G (n.-155T>G) c.112T>G (p.Ser38Ala) | dbSNP |
| 8 | g.127738409C>A | CA372279562 | MYC | c.147C>A (p.Ile49=) c.189C>A (p.Ile63=) c.192C>A (p.Ile64=) c.-154C>A (n.-154C>A) c.113C>A (p.Ser38Tyr) | |
| 8 | g.127738409C>G | CA372279563 | MYC | c.147C>G (p.Ile49Met) c.189C>G (p.Ile63Met) c.192C>G (p.Ile64Met) c.-154C>G (n.-154C>G) c.113C>G (p.Ser38Cys) | dbSNP |
| 8 | g.127738409C>T | CA372279564 | MYC | c.147C>T (p.Ile49=) c.189C>T (p.Ile63=) c.192C>T (p.Ile64=) c.-154C>T (n.-154C>T) c.113C>T (p.Ser38Phe) | dbSNP |
| 8 | g.127738410T>A | CA372279565 | MYC | c.148T>A (p.Trp50Arg) c.190T>A (p.Trp64Arg) c.193T>A (p.Trp65Arg) c.-153T>A (n.-153T>A) c.114T>A (p.Ser38=) | |
| 8 | g.127738410T>C | CA372279566 | MYC | c.148T>C (p.Trp50Arg) c.190T>C (p.Trp64Arg) c.193T>C (p.Trp65Arg) c.-153T>C (n.-153T>C) c.114T>C (p.Ser38=) | |
| 8 | g.127738410T>G | CA372279567 | MYC | c.148T>G (p.Trp50Gly) c.190T>G (p.Trp64Gly) c.193T>G (p.Trp65Gly) c.-153T>G (n.-153T>G) c.114T>G (p.Ser38=) | |
| 8 | g.127738411G>A | CA372279570 | MYC | c.149G>A (p.Trp50Ter) c.191G>A (p.Trp64Ter) c.194G>A (p.Trp65Ter) c.-152G>A (n.-152G>A) c.115G>A (p.Gly39Arg) | dbSNP |
| 8 | g.127738411G>C | CA372279569 | MYC | c.149G>C (p.Trp50Ser) c.191G>C (p.Trp64Ser) c.194G>C (p.Trp65Ser) c.-152G>C (n.-152G>C) c.115G>C (p.Gly39Arg) | dbSNP |
| 8 | g.127738411G>T | CA372279568 | MYC | c.149G>T (p.Trp50Leu) c.191G>T (p.Trp64Leu) c.194G>T (p.Trp65Leu) c.-152G>T (n.-152G>T) c.115G>T (p.Gly39Ter) | dbSNP |
| 8 | g.127738412G>A | CA372279573 | MYC | c.150G>A (p.Trp50Ter) c.192G>A (p.Trp64Ter) c.195G>A (p.Trp65Ter) c.-151G>A (n.-151G>A) c.116G>A (p.Gly39Glu) | dbSNP |
| 8 | g.127738412G>C | CA372279571 | MYC | c.150G>C (p.Trp50Cys) c.192G>C (p.Trp64Cys) c.195G>C (p.Trp65Cys) c.-151G>C (n.-151G>C) c.116G>C (p.Gly39Ala) | dbSNP |
| 8 | g.127738412G>T | CA372279572 | MYC | c.150G>T (p.Trp50Cys) c.192G>T (p.Trp64Cys) c.195G>T (p.Trp65Cys) c.-151G>T (n.-151G>T) c.116G>T (p.Gly39Val) | dbSNP |
| 8 | g.127738413A>C | CA372279574 | MYC | c.151A>C (p.Lys51Gln) c.193A>C (p.Lys65Gln) c.196A>C (p.Lys66Gln) c.-150A>C (n.-150A>C) c.117A>C (p.Gly39=) | |
| 8 | g.127738413A>G | CA372279575 | MYC | c.151A>G (p.Lys51Glu) c.193A>G (p.Lys65Glu) c.196A>G (p.Lys66Glu) c.-150A>G (n.-150A>G) c.117A>G (p.Gly39=) | gnomAD v4 |
| 8 | g.127738413A>T | CA372279576 | MYC | c.151A>T (p.Lys51Ter) c.193A>T (p.Lys65Ter) c.196A>T (p.Lys66Ter) c.-150A>T (n.-150A>T) c.117A>T (p.Gly39=) | dbSNP |
| 8 | g.127738414A>C | CA372279579 | MYC | c.152A>C (p.Lys51Thr) c.194A>C (p.Lys65Thr) c.197A>C (p.Lys66Thr) c.-149A>C (n.-149A>C) c.118A>C (p.Arg40=) | |
| 8 | g.127738414A>G | CA372279578 | MYC | c.152A>G (p.Lys51Arg) c.194A>G (p.Lys65Arg) c.197A>G (p.Lys66Arg) c.-149A>G (n.-149A>G) c.118A>G (p.Arg40Gly) | dbSNP |
| 8 | g.127738414A>T | CA372279577 | MYC | c.152A>T (p.Lys51Met) c.194A>T (p.Lys65Met) c.197A>T (p.Lys66Met) c.-149A>T (n.-149A>T) c.118A>T (p.Arg40Ter) | dbSNP |
| 8 | g.127738415G>A | CA372279580 | MYC | c.153G>A (p.Lys51=) c.195G>A (p.Lys65=) c.198G>A (p.Lys66=) c.-148G>A (n.-148G>A) c.119G>A (p.Arg40Lys) | dbSNP |
| 8 | g.127738415G>C | CA372279581 | MYC | c.153G>C (p.Lys51Asn) c.195G>C (p.Lys65Asn) c.198G>C (p.Lys66Asn) c.-148G>C (n.-148G>C) c.119G>C (p.Arg40Thr) | dbSNP |
| 8 | g.127738415G>T | CA372279582 | MYC | c.153G>T (p.Lys51Asn) c.195G>T (p.Lys65Asn) c.198G>T (p.Lys66Asn) c.-148G>T (n.-148G>T) c.119G>T (p.Arg40Ile) | dbSNP COSMIC COSMIC |
| 8 | g.127738416A>C | CA372279583 | MYC | c.154A>C (p.Lys52Gln) c.196A>C (p.Lys66Gln) c.199A>C (p.Lys67Gln) c.-147A>C (n.-147A>C) c.120A>C (p.Arg40Ser) | |
| 8 | g.127738416A>G | CA372279584 | MYC | c.154A>G (p.Lys52Glu) c.196A>G (p.Lys66Glu) c.199A>G (p.Lys67Glu) c.-147A>G (n.-147A>G) c.120A>G (p.Arg40=) | |
| 8 | g.127738416A>T | CA372279585 | MYC | c.154A>T (p.Lys52Ter) c.196A>T (p.Lys66Ter) c.199A>T (p.Lys67Ter) c.-147A>T (n.-147A>T) c.120A>T (p.Arg40Ser) | dbSNP |
| 8 | g.127738417A>C | CA372279586 | MYC | c.155A>C (p.Lys52Thr) c.197A>C (p.Lys66Thr) c.200A>C (p.Lys67Thr) c.-146A>C (n.-146A>C) c.121A>C (p.Asn41His) | |
| 8 | g.127738417A>G | CA372279588 | MYC | c.155A>G (p.Lys52Arg) c.197A>G (p.Lys66Arg) c.200A>G (p.Lys67Arg) c.-146A>G (n.-146A>G) c.121A>G (p.Asn41Asp) | dbSNP |
| 8 | g.127738417A>T | CA372279587 | MYC | c.155A>T (p.Lys52Ile) c.197A>T (p.Lys66Ile) c.200A>T (p.Lys67Ile) c.-146A>T (n.-146A>T) c.121A>T (p.Asn41Tyr) | dbSNP |
| 8 | g.127738418A>C | CA372279589 | MYC | c.156A>C (p.Lys52Asn) c.198A>C (p.Lys66Asn) c.201A>C (p.Lys67Asn) c.-145A>C (n.-145A>C) c.122A>C (p.Asn41Thr) | dbSNP |
| 8 | g.127738418A>G | CA372279590 | MYC | c.156A>G (p.Lys52=) c.198A>G (p.Lys66=) c.201A>G (p.Lys67=) c.-145A>G (n.-145A>G) c.122A>G (p.Asn41Ser) | dbSNP |
| 8 | g.127738418A>T | CA372279591 | MYC | c.156A>T (p.Lys52Asn) c.198A>T (p.Lys66Asn) c.201A>T (p.Lys67Asn) c.-145A>T (n.-145A>T) c.122A>T (p.Asn41Ile) | dbSNP |
| 8 | g.127738419T>A | CA372279592 | MYC | c.157T>A (p.Phe53Ile) c.199T>A (p.Phe67Ile) c.202T>A (p.Phe68Ile) c.-144T>A (n.-144T>A) c.123T>A (p.Asn41Lys) | dbSNP |
| 8 | g.127738419T>C | CA372279593 | MYC | c.157T>C (p.Phe53Leu) c.199T>C (p.Phe67Leu) c.202T>C (p.Phe68Leu) c.-144T>C (n.-144T>C) c.123T>C (p.Asn41=) | |
| 8 | g.127738419T>G | CA372279594 | MYC | c.157T>G (p.Phe53Val) c.199T>G (p.Phe67Val) c.202T>G (p.Phe68Val) c.-144T>G (n.-144T>G) c.123T>G (p.Asn41Lys) | dbSNP |
| 8 | g.127738420T>A | CA372279595 | MYC | c.158T>A (p.Phe53Tyr) c.200T>A (p.Phe67Tyr) c.203T>A (p.Phe68Tyr) c.-143T>A (n.-143T>A) c.124T>A (p.Ser42Thr) | dbSNP |
| 8 | g.127738420T>C | CA372279596 | MYC | c.158T>C (p.Phe53Ser) c.200T>C (p.Phe67Ser) c.203T>C (p.Phe68Ser) c.-143T>C (n.-143T>C) c.124T>C (p.Ser42Pro) | dbSNP |
| 8 | g.127738420T>G | CA372279597 | MYC | c.158T>G (p.Phe53Cys) c.200T>G (p.Phe67Cys) c.203T>G (p.Phe68Cys) c.-143T>G (n.-143T>G) c.124T>G (p.Ser42Ala) | |
| 8 | g.127738421C>A | CA372279598 | MYC | c.159C>A (p.Phe53Leu) c.201C>A (p.Phe67Leu) c.204C>A (p.Phe68Leu) c.-142C>A (n.-142C>A) c.125C>A (p.Ser42Ter) | dbSNP |
| 8 | g.127738421C= | CA1818466402 | MYC | c.159C= (p.Phe53=) c.201C= (p.Phe67=) c.204C= (p.Phe68=) c.-142C= (n.-142C=) c.125C= (p.Ser42=) | |
| 8 | g.127738421C>G | CA372279599 | MYC | c.159C>G (p.Phe53Leu) c.201C>G (p.Phe67Leu) c.204C>G (p.Phe68Leu) c.-142C>G (n.-142C>G) c.125C>G (p.Ser42Trp) | dbSNP |
| 8 | g.127738421C>T | CA4875247 | MYC | c.159C>T (p.Phe53=) c.201C>T (p.Phe67=) c.204C>T (p.Phe68=) c.-142C>T (n.-142C>T) c.125C>T (p.Ser42Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738422G>A | CA372279601 | MYC | c.160G>A (p.Glu54Lys) c.202G>A (p.Glu68Lys) c.205G>A (p.Glu69Lys) c.-141G>A (n.-141G>A) c.126G>A (p.Ser42=) | dbSNP |
| 8 | g.127738422G>C | CA372279602 | MYC | c.160G>C (p.Glu54Gln) c.202G>C (p.Glu68Gln) c.205G>C (p.Glu69Gln) c.-141G>C (n.-141G>C) c.126G>C (p.Ser42=) | dbSNP |
| 8 | g.127738422G>T | CA372279600 | MYC | c.160G>T (p.Glu54Ter) c.202G>T (p.Glu68Ter) c.205G>T (p.Glu69Ter) c.-141G>T (n.-141G>T) c.126G>T (p.Ser42=) | dbSNP |
| 8 | g.127738423A>C | CA372279603 | MYC | c.161A>C (p.Glu54Ala) c.203A>C (p.Glu68Ala) c.206A>C (p.Glu69Ala) c.-140A>C (n.-140A>C) c.127A>C (p.Ser43Arg) | |
| 8 | g.127738423A>G | CA372279604 | MYC | c.161A>G (p.Glu54Gly) c.203A>G (p.Glu68Gly) c.206A>G (p.Glu69Gly) c.-140A>G (n.-140A>G) c.127A>G (p.Ser43Gly) | dbSNP |
| 8 | g.127738423A>T | CA372279605 | MYC | c.161A>T (p.Glu54Val) c.203A>T (p.Glu68Val) c.206A>T (p.Glu69Val) c.-140A>T (n.-140A>T) c.127A>T (p.Ser43Cys) | dbSNP |
| 8 | g.127738423_127738426delinsAGCT | CA1818466407 | MYC | c.161_164delinsAGCT (p.Glu54=) c.203_206delinsAGCT (p.Glu68=) c.206_209delinsAGCT (p.Glu69=) c.-140_-137delinsAGCT (n.-140_-137delinsAGCT) c.127_130delinsAGCT (p.Ser43=) | |
| 8 | g.127738424G>A | CA372279606 | MYC | c.162G>A (p.Glu54=) c.204G>A (p.Glu68=) c.207G>A (p.Glu69=) c.-139G>A (n.-139G>A) c.128G>A (p.Ser43Asn) | dbSNP |
| 8 | g.127738424G>C | CA372279607 | MYC | c.162G>C (p.Glu54Asp) c.204G>C (p.Glu68Asp) c.207G>C (p.Glu69Asp) c.-139G>C (n.-139G>C) c.128G>C (p.Ser43Thr) | dbSNP |
| 8 | g.127738424G>T | CA372279608 | MYC | c.162G>T (p.Glu54Asp) c.204G>T (p.Glu68Asp) c.207G>T (p.Glu69Asp) c.-139G>T (n.-139G>T) c.128G>T (p.Ser43Ile) | |
| 8 | g.127738429_127738431del | CA4875248 | MYC | c.167_169del (p.Leu56del) c.209_211del (p.Leu70del) c.212_214del (p.Leu71del) c.-134_-132del (n.-134_-132del) c.133_135del (p.Cys45del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738425C>A | CA372279610 | MYC | c.163C>A (p.Leu55Met) c.205C>A (p.Leu69Met) c.208C>A (p.Leu70Met) c.-138C>A (n.-138C>A) c.129C>A (p.Ser43Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.127738425C= | CA1818466412 | MYC | c.163C= (p.Leu55=) c.205C= (p.Leu69=) c.208C= (p.Leu70=) c.-138C= (n.-138C=) c.129C= (p.Ser43=) | |
| 8 | g.127738425C>G | CA372279609 | MYC | c.163C>G (p.Leu55Val) c.205C>G (p.Leu69Val) c.208C>G (p.Leu70Val) c.-138C>G (n.-138C>G) c.129C>G (p.Ser43Arg) | dbSNP |
| 8 | g.127738425C>T | CA462987840 | MYC | c.163C>T (p.Leu55=) c.205C>T (p.Leu69=) c.208C>T (p.Leu70=) c.-138C>T (n.-138C>T) c.129C>T (p.Ser43=) | dbSNP COSMIC COSMIC |
| 8 | g.127738426T>A | CA372279611 | MYC | c.164T>A (p.Leu55Gln) c.206T>A (p.Leu69Gln) c.209T>A (p.Leu70Gln) c.-137T>A (n.-137T>A) c.130T>A (p.Cys44Ser) | dbSNP |
| 8 | g.127738426T>C | CA372279612 | MYC | c.164T>C (p.Leu55Pro) c.206T>C (p.Leu69Pro) c.209T>C (p.Leu70Pro) c.-137T>C (n.-137T>C) c.130T>C (p.Cys44Arg) | dbSNP |
| 8 | g.127738426T>G | CA372279613 | MYC | c.164T>G (p.Leu55Arg) c.206T>G (p.Leu69Arg) c.209T>G (p.Leu70Arg) c.-137T>G (n.-137T>G) c.130T>G (p.Cys44Gly) | |
| 8 | g.127738427G>A | CA372279614 | MYC | c.165G>A (p.Leu55=) c.207G>A (p.Leu69=) c.210G>A (p.Leu70=) c.-136G>A (n.-136G>A) c.131G>A (p.Cys44Tyr) | dbSNP gnomAD v4 COSMIC COSMIC |
| 8 | g.127738427G>C | CA372279615 | MYC | c.165G>C (p.Leu55=) c.207G>C (p.Leu69=) c.210G>C (p.Leu70=) c.-136G>C (n.-136G>C) c.131G>C (p.Cys44Ser) | dbSNP |
| 8 | g.127738427G>T | CA372279616 | MYC | c.165G>T (p.Leu55=) c.207G>T (p.Leu69=) c.210G>T (p.Leu70=) c.-136G>T (n.-136G>T) c.131G>T (p.Cys44Phe) | dbSNP COSMIC COSMIC |
| 8 | g.127738428C>A | CA372279617 | MYC | c.166C>A (p.Leu56Met) c.208C>A (p.Leu70Met) c.211C>A (p.Leu71Met) c.-135C>A (n.-135C>A) c.132C>A (p.Cys44Ter) | dbSNP |
| 8 | g.127738428C= | CA1818466415 | MYC | c.166C= (p.Leu56=) c.208C= (p.Leu70=) c.211C= (p.Leu71=) c.-135C= (n.-135C=) c.132C= (p.Cys44=) | |
| 8 | g.127738428C>G | CA372279618 | MYC | c.166C>G (p.Leu56Val) c.208C>G (p.Leu70Val) c.211C>G (p.Leu71Val) c.-135C>G (n.-135C>G) c.132C>G (p.Cys44Trp) | dbSNP |
| 8 | g.127738428C>T | CA4875249 | MYC | c.166C>T (p.Leu56=) c.208C>T (p.Leu70=) c.211C>T (p.Leu71=) c.-135C>T (n.-135C>T) c.132C>T (p.Cys44=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738429T>A | CA372279619 | MYC | c.167T>A (p.Leu56Gln) c.209T>A (p.Leu70Gln) c.212T>A (p.Leu71Gln) c.-134T>A (n.-134T>A) c.133T>A (p.Cys45Ser) | dbSNP |
| 8 | g.127738429T>C | CA372279620 | MYC | c.167T>C (p.Leu56Pro) c.209T>C (p.Leu70Pro) c.212T>C (p.Leu71Pro) c.-134T>C (n.-134T>C) c.133T>C (p.Cys45Arg) | dbSNP |
| 8 | g.127738429T>G | CA372279621 | MYC | c.167T>G (p.Leu56Arg) c.209T>G (p.Leu70Arg) c.212T>G (p.Leu71Arg) c.-134T>G (n.-134T>G) c.133T>G (p.Cys45Gly) | |
| 8 | g.127738430G>A | CA372279622 | MYC | c.168G>A (p.Leu56=) c.210G>A (p.Leu70=) c.213G>A (p.Leu71=) c.-133G>A (n.-133G>A) c.134G>A (p.Cys45Tyr) | |
| 8 | g.127738430G>C | CA372279623 | MYC | c.168G>C (p.Leu56=) c.210G>C (p.Leu70=) c.213G>C (p.Leu71=) c.-133G>C (n.-133G>C) c.134G>C (p.Cys45Ser) | |
| 8 | g.127738430G>T | CA372279624 | MYC | c.168G>T (p.Leu56=) c.210G>T (p.Leu70=) c.213G>T (p.Leu71=) c.-133G>T (n.-133G>T) c.134G>T (p.Cys45Phe) | |
| 8 | g.127738431C>A | CA372279625 | MYC | c.169C>A (p.Pro57Thr) c.211C>A (p.Pro71Thr) c.214C>A (p.Pro72Thr) c.-132C>A (n.-132C>A) c.135C>A (p.Cys45Ter) | COSMIC COSMIC |
| 8 | g.127738431C= | CA1818466422 | MYC | c.169C= (p.Pro57=) c.211C= (p.Pro71=) c.214C= (p.Pro72=) c.-132C= (n.-132C=) c.135C= (p.Cys45=) | |
| 8 | g.127738431C>G | CA372279626 | MYC | c.169C>G (p.Pro57Ala) c.211C>G (p.Pro71Ala) c.214C>G (p.Pro72Ala) c.-132C>G (n.-132C>G) c.135C>G (p.Cys45Trp) | dbSNP COSMIC COSMIC |
| 8 | g.127738431C>T | CA122520 | MYC | c.169C>T (p.Pro57Ser) c.211C>T (p.Pro71Ser) c.214C>T (p.Pro72Ser) c.-132C>T (n.-132C>T) c.135C>T (p.Cys45=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738431_127738433del | CA645565237 | MYC | c.169_171del (p.Pro57del) c.211_213del (p.Pro71del) c.214_216del (p.Pro72del) c.-132_-130del (n.-132_-130del) c.135_137del (p.Cys45Ter) | COSMIC COSMIC |
| 8 | g.127738432C>A | CA372279627 | MYC | c.170C>A (p.Pro57His) c.212C>A (p.Pro71His) c.215C>A (p.Pro72His) c.-131C>A (n.-131C>A) c.136C>A (p.Pro46Thr) | dbSNP |
| 8 | g.127738432C>G | CA372279628 | MYC | c.170C>G (p.Pro57Arg) c.212C>G (p.Pro71Arg) c.215C>G (p.Pro72Arg) c.-131C>G (n.-131C>G) c.136C>G (p.Pro46Ala) | dbSNP |
| 8 | g.127738432C>T | CA372279629 | MYC | c.170C>T (p.Pro57Leu) c.212C>T (p.Pro71Leu) c.215C>T (p.Pro72Leu) c.-131C>T (n.-131C>T) c.136C>T (p.Pro46Ser) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738433C>A | CA372279630 | MYC | c.171C>A (p.Pro57=) c.213C>A (p.Pro71=) c.216C>A (p.Pro72=) c.-130C>A (n.-130C>A) c.137C>A (p.Pro46Gln) | dbSNP gnomAD v4 |
| 8 | g.127738433C= | CA1818466428 | MYC | c.171C= (p.Pro57=) c.213C= (p.Pro71=) c.216C= (p.Pro72=) c.-130C= (n.-130C=) c.137C= (p.Pro46=) | |
| 8 | g.127738433C>G | CA372279632 | MYC | c.171C>G (p.Pro57=) c.213C>G (p.Pro71=) c.216C>G (p.Pro72=) c.-130C>G (n.-130C>G) c.137C>G (p.Pro46Arg) | |
| 8 | g.127738433C>T | CA372279631 | MYC | c.171C>T (p.Pro57=) c.213C>T (p.Pro71=) c.216C>T (p.Pro72=) c.-130C>T (n.-130C>T) c.137C>T (p.Pro46Leu) | dbSNP |
| 8 | g.127738434A= | CA1818466435 | MYC | c.172A= (p.Thr58=) c.214A= (p.Thr72=) c.217A= (p.Thr73=) c.-129A= (n.-129A=) c.138A= (p.Pro46=) | |
| 8 | g.127738434A>C | CA4875250 | MYC | c.172A>C (p.Thr58Pro) c.214A>C (p.Thr72Pro) c.217A>C (p.Thr73Pro) c.-129A>C (n.-129A>C) c.138A>C (p.Pro46=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.127738434A>G | CA372279633 | MYC | c.172A>G (p.Thr58Ala) c.214A>G (p.Thr72Ala) c.217A>G (p.Thr73Ala) c.-129A>G (n.-129A>G) c.138A>G (p.Pro46=) | ClinVar dbSNP COSMIC COSMIC |
| 8 | g.127738434A>T | CA372279634 | MYC | c.172A>T (p.Thr58Ser) c.214A>T (p.Thr72Ser) c.217A>T (p.Thr73Ser) c.-129A>T (n.-129A>T) c.138A>T (p.Pro46=) | |
| 8 | g.127738435C>A | CA372279635 | MYC | c.173C>A (p.Thr58Asn) c.215C>A (p.Thr72Asn) c.218C>A (p.Thr73Asn) c.-128C>A (n.-128C>A) c.139C>A (p.Pro47Thr) | COSMIC COSMIC |
| 8 | g.127738435C= | CA1818466441 | MYC | c.173C= (p.Thr58=) c.215C= (p.Thr72=) c.218C= (p.Thr73=) c.-128C= (n.-128C=) c.139C= (p.Pro47=) | |
| 8 | g.127738435C>G | CA4875251 | MYC | c.173C>G (p.Thr58Ser) c.215C>G (p.Thr72Ser) c.218C>G (p.Thr73Ser) c.-128C>G (n.-128C>G) c.139C>G (p.Pro47Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738435C>T | CA16602746 | MYC | c.173C>T (p.Thr58Ile) c.215C>T (p.Thr72Ile) c.218C>T (p.Thr73Ile) c.-128C>T (n.-128C>T) c.139C>T (p.Pro47Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738435_127738436delinsGT | CA2573332804 | MYC | c.173_174delinsGT (p.Thr58Ser) c.215_216delinsGT (p.Thr72Ser) c.218_219delinsGT (p.Thr73Ser) c.-128_-127delinsGT (n.-128_-127delinsGT) c.139_140delinsGT (p.Pro47Val) | |
| 8 | g.127738438del | CA2502800997 | MYC | c.176del (p.Pro59ArgfsTer?) c.218del (p.Pro73ArgfsTer?) c.221del (p.Pro74ArgfsTer?) c.-125del (n.-125del) c.142del (p.Arg48AlafsTer5) | |
| 8 | g.127738436_127738438del | CA2573332252 | MYC | c.174_176del (p.Pro59del) c.216_218del (p.Pro73del) c.219_221del (p.Pro74del) c.-127_-125del (n.-127_-125del) c.140_142del (p.Pro47del) | |
| 8 | g.127738435_127738443del | CA645565238 | MYC | c.173_181del (p.Thr58_Leu61delinsMet) c.215_223del (p.Thr72_Leu75delinsMet) c.218_226del (p.Thr73_Leu76delinsMet) c.-128_-120del (n.-128_-120del) c.139_147del (p.Pro47_Pro49del) | COSMIC COSMIC |
| 8 | g.127738436C>A | CA372279636 | MYC | c.174C>A (p.Thr58=) c.216C>A (p.Thr72=) c.219C>A (p.Thr73=) c.-127C>A (n.-127C>A) c.140C>A (p.Pro47His) | dbSNP gnomAD v4 |
| 8 | g.127738436C= | CA1818466447 | MYC | c.174C= (p.Thr58=) c.216C= (p.Thr72=) c.219C= (p.Thr73=) c.-127C= (n.-127C=) c.140C= (p.Pro47=) | |
| 8 | g.127738436C>G | CA372279637 | MYC | c.174C>G (p.Thr58=) c.216C>G (p.Thr72=) c.219C>G (p.Thr73=) c.-127C>G (n.-127C>G) c.140C>G (p.Pro47Arg) | |
| 8 | g.127738436C>T | CA372279638 | MYC | c.174C>T (p.Thr58=) c.216C>T (p.Thr72=) c.219C>T (p.Thr73=) c.-127C>T (n.-127C>T) c.140C>T (p.Pro47Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 8 | g.127738437C>A | CA372279639 | MYC | c.175C>A (p.Pro59Thr) c.217C>A (p.Pro73Thr) c.220C>A (p.Pro74Thr) c.-126C>A (n.-126C>A) c.141C>A (p.Pro47=) | dbSNP COSMIC COSMIC |
| 8 | g.127738437C= | CA1818466452 | MYC | c.175C= (p.Pro59=) c.217C= (p.Pro73=) c.220C= (p.Pro74=) c.-126C= (n.-126C=) c.141C= (p.Pro47=) | |
| 8 | g.127738437C>G | CA122526 | MYC | c.175C>G (p.Pro59Ala) c.217C>G (p.Pro73Ala) c.220C>G (p.Pro74Ala) c.-126C>G (n.-126C>G) c.141C>G (p.Pro47=) | ClinVar dbSNP COSMIC COSMIC |
| 8 | g.127738437C>T | CA372279640 | MYC | c.175C>T (p.Pro59Ser) c.217C>T (p.Pro73Ser) c.220C>T (p.Pro74Ser) c.-126C>T (n.-126C>T) c.141C>T (p.Pro47=) | dbSNP COSMIC COSMIC |
| 8 | g.127738438C>A | CA16040251 | MYC | c.176C>A (p.Pro59Gln) c.218C>A (p.Pro73Gln) c.221C>A (p.Pro74Gln) c.-125C>A (n.-125C>A) c.142C>A (p.Arg48Ser) | dbSNP gnomAD v4 COSMIC COSMIC |
| 8 | g.127738438C= | CA1818466458 | MYC | c.176C= (p.Pro59=) c.218C= (p.Pro73=) c.221C= (p.Pro74=) c.-125C= (n.-125C=) c.142C= (p.Arg48=) | |
| 8 | g.127738438C>G | CA372279641 | MYC | c.176C>G (p.Pro59Arg) c.218C>G (p.Pro73Arg) c.221C>G (p.Pro74Arg) c.-125C>G (n.-125C>G) c.142C>G (p.Arg48Gly) | dbSNP COSMIC |
| 8 | g.127738438C>T | CA372279642 | MYC | c.176C>T (p.Pro59Leu) c.218C>T (p.Pro73Leu) c.221C>T (p.Pro74Leu) c.-125C>T (n.-125C>T) c.142C>T (p.Arg48Cys) | dbSNP gnomAD v2 COSMIC COSMIC |
| 8 | g.127738439G>A | CA372279643 | MYC | c.177G>A (p.Pro59=) c.219G>A (p.Pro73=) c.222G>A (p.Pro74=) c.-124G>A (n.-124G>A) c.143G>A (p.Arg48His) | |
| 8 | g.127738439G>C | CA372279644 | MYC | c.177G>C (p.Pro59=) c.219G>C (p.Pro73=) c.222G>C (p.Pro74=) c.-124G>C (n.-124G>C) c.143G>C (p.Arg48Pro) | gnomAD v4 |
| 8 | g.127738439G>T | CA372279645 | MYC | c.177G>T (p.Pro59=) c.219G>T (p.Pro73=) c.222G>T (p.Pro74=) c.-124G>T (n.-124G>T) c.143G>T (p.Arg48Leu) | |
| 8 | g.127738440C>A | CA372279646 | MYC | c.178C>A (p.Pro60Thr) c.220C>A (p.Pro74Thr) c.223C>A (p.Pro75Thr) c.-123C>A (n.-123C>A) c.144C>A (p.Arg48=) | ClinVar dbSNP COSMIC |
| 8 | g.127738440C>G | CA372279647 | MYC | c.178C>G (p.Pro60Ala) c.220C>G (p.Pro74Ala) c.223C>G (p.Pro75Ala) c.-123C>G (n.-123C>G) c.144C>G (p.Arg48=) | dbSNP COSMIC COSMIC |
| 8 | g.127738440C>T | CA372279648 | MYC | c.178C>T (p.Pro60Ser) c.220C>T (p.Pro74Ser) c.223C>T (p.Pro75Ser) c.-123C>T (n.-123C>T) c.144C>T (p.Arg48=) | dbSNP COSMIC COSMIC |
| 8 | g.127738440_127738441insTGGACCCCG | CA645565239 | MYC | c.178_179insTGGACCCCG (p.Pro60delinsLeuAspProAla) c.220_221insTGGACCCCG (p.Pro74delinsLeuAspProAla) c.223_224insTGGACCCCG (p.Pro75delinsLeuAspProAla) c.-123_-122insTGGACCCCG (n.-123_-122insTGGACCCCG) c.144_145insTGGACCCCG (p.Arg48_Pro49insTrpThrPro) | COSMIC COSMIC |
| 8 | g.127738441C>A | CA372279649 | MYC | c.179C>A (p.Pro60His) c.221C>A (p.Pro74His) c.224C>A (p.Pro75His) c.-122C>A (n.-122C>A) c.145C>A (p.Pro49Thr) | COSMIC COSMIC |
| 8 | g.127738441C>G | CA372279650 | MYC | c.179C>G (p.Pro60Arg) c.221C>G (p.Pro74Arg) c.224C>G (p.Pro75Arg) c.-122C>G (n.-122C>G) c.145C>G (p.Pro49Ala) | dbSNP |
| 8 | g.127738441C>T | CA372279651 | MYC | c.179C>T (p.Pro60Leu) c.221C>T (p.Pro74Leu) c.224C>T (p.Pro75Leu) c.-122C>T (n.-122C>T) c.145C>T (p.Pro49Ser) | dbSNP COSMIC |
| 8 | g.127738442C>A | CA372279652 | MYC | c.180C>A (p.Pro60=) c.222C>A (p.Pro74=) c.225C>A (p.Pro75=) c.-121C>A (n.-121C>A) c.146C>A (p.Pro49His) | dbSNP |
| 8 | g.127738442C>G | CA372279653 | MYC | c.180C>G (p.Pro60=) c.222C>G (p.Pro74=) c.225C>G (p.Pro75=) c.-121C>G (n.-121C>G) c.146C>G (p.Pro49Arg) | dbSNP |
| 8 | g.127738442C>T | CA372279654 | MYC | c.180C>T (p.Pro60=) c.222C>T (p.Pro74=) c.225C>T (p.Pro75=) c.-121C>T (n.-121C>T) c.146C>T (p.Pro49Leu) | dbSNP COSMIC COSMIC |
| 8 | g.127738443C>A | CA372279656 | MYC | c.181C>A (p.Leu61Met) c.223C>A (p.Leu75Met) c.226C>A (p.Leu76Met) c.-120C>A (n.-120C>A) c.147C>A (p.Pro49=) | dbSNP |
| 8 | g.127738443C= | CA1818466462 | MYC | c.181C= (p.Leu61=) c.223C= (p.Leu75=) c.226C= (p.Leu76=) c.-120C= (n.-120C=) c.147C= (p.Pro49=) | |
| 8 | g.127738443C>G | CA372279655 | MYC | c.181C>G (p.Leu61Val) c.223C>G (p.Leu75Val) c.226C>G (p.Leu76Val) c.-120C>G (n.-120C>G) c.147C>G (p.Pro49=) | |
| 8 | g.127738443C>T | CA462987969 | MYC | c.181C>T (p.Leu61=) c.223C>T (p.Leu75=) c.226C>T (p.Leu76=) c.-120C>T (n.-120C>T) c.147C>T (p.Pro49=) | dbSNP gnomAD v2 gnomAD v4 |
| 8 | g.127738444T>A | CA372279657 | MYC | c.182T>A (p.Leu61Gln) c.224T>A (p.Leu75Gln) c.227T>A (p.Leu76Gln) c.-119T>A (n.-119T>A) c.148T>A (p.Cys50Ser) | dbSNP |
| 8 | g.127738444T>C | CA372279658 | MYC | c.182T>C (p.Leu61Pro) c.224T>C (p.Leu75Pro) c.227T>C (p.Leu76Pro) c.-119T>C (n.-119T>C) c.148T>C (p.Cys50Arg) | dbSNP |
| 8 | g.127738444T>G | CA4875252 | MYC | c.182T>G (p.Leu61Arg) c.224T>G (p.Leu75Arg) c.227T>G (p.Leu76Arg) c.-119T>G (n.-119T>G) c.148T>G (p.Cys50Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 8 | g.127738444T= | CA1818466465 | MYC | c.182T= (p.Leu61=) c.224T= (p.Leu75=) c.227T= (p.Leu76=) c.-119T= (n.-119T=) c.148T= (p.Cys50=) |