Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.151680737C>A | CA348820997 | NEB | c.3035G>T (p.Arg1012Met) | |
2 | g.151680737C>G | CA348820998 | NEB | c.3035G>C (p.Arg1012Thr) | |
2 | g.151680737C>T | CA348820999 | NEB | c.3035G>A (p.Arg1012Lys) | |
2 | g.151680738T>A | CA348821001 | NEB | c.3034A>T (p.Arg1012Trp) | |
2 | g.151680738T>C | CA348821000 | NEB | c.3034A>G (p.Arg1012Gly) | |
2 | g.151680738T>G | CA429243793 | NEB | c.3034A>C (p.Arg1012=) | |
2 | g.151680739C>A | CA348821002 | NEB | c.3033G>T (p.Gln1011His) | |
2 | g.151680739C= | CA1298292519 | NEB | c.3033G= (p.Gln1011=) | |
2 | g.151680739C>G | CA348821003 | NEB | c.3033G>C (p.Gln1011His) | dbSNP gnomAD v4 |
2 | g.151680739C>T | CA429243794 | NEB | c.3033G>A (p.Gln1011=) | |
2 | g.151680740T>A | CA348821004 | NEB | c.3032A>T (p.Gln1011Leu) | |
2 | g.151680740T>C | CA348821005 | NEB | c.3032A>G (p.Gln1011Arg) | |
2 | g.151680740T>G | CA348821006 | NEB | c.3032A>C (p.Gln1011Pro) | |
2 | g.151680741G>A | CA348821007 | NEB | c.3031C>T (p.Gln1011Ter) | |
2 | g.151680741G>C | CA348821008 | NEB | c.3031C>G (p.Gln1011Glu) | |
2 | g.151680741G>T | CA348821009 | NEB | c.3031C>A (p.Gln1011Lys) | gnomAD v4 |
2 | g.151680742G>A | CA429243795 | NEB | c.3030C>T (p.Ala1010=) | |
2 | g.151680742G>C | CA429243796 | NEB | c.3030C>G (p.Ala1010=) | gnomAD v4 |
2 | g.151680742G>T | CA429243797 | NEB | c.3030C>A (p.Ala1010=) | ClinVar dbSNP |
2 | g.151680743G>A | CA1911041 | NEB | c.3029C>T (p.Ala1010Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.151680743G>C | CA348821010 | NEB | c.3029C>G (p.Ala1010Gly) | gnomAD v4 |
2 | g.151680743G= | CA1298292521 | NEB | c.3029C= (p.Ala1010=) | |
2 | g.151680743G>T | CA348821011 | NEB | c.3029C>A (p.Ala1010Asp) | gnomAD v4 |
2 | g.151680744C>A | CA348821012 | NEB | c.3028G>T (p.Ala1010Ser) | dbSNP gnomAD v4 |
2 | g.151680744C= | CA1298292525 | NEB | c.3028G= (p.Ala1010=) | |
2 | g.151680744C>G | CA348821013 | NEB | c.3028G>C (p.Ala1010Pro) | ClinVar dbSNP |
2 | g.151680744C>T | CA1911042 | NEB | c.3028G>A (p.Ala1010Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.151680745C>A | CA348821015 | NEB | c.3027G>T (p.Gln1009His) | |
2 | g.151680745C>G | CA348821014 | NEB | c.3027G>C (p.Gln1009His) | |
2 | g.151680745C>T | CA429243798 | NEB | c.3027G>A (p.Gln1009=) | ClinVar dbSNP gnomAD v4 |
2 | g.151680746T>A | CA348821016 | NEB | c.3026A>T (p.Gln1009Leu) | |
2 | g.151680746T>C | CA348821017 | NEB | c.3026A>G (p.Gln1009Arg) | gnomAD v4 |
2 | g.151680746T>G | CA348821018 | NEB | c.3026A>C (p.Gln1009Pro) | COSMIC COSMIC COSMIC |
2 | g.151680747G>A | CA348821019 | NEB | c.3025C>T (p.Gln1009Ter) | ClinVar |
2 | g.151680747G>C | CA348821020 | NEB | c.3025C>G (p.Gln1009Glu) | |
2 | g.151680747G>T | CA348821021 | NEB | c.3025C>A (p.Gln1009Lys) | gnomAD v4 |
2 | g.151680748G>A | CA429243799 | NEB | c.3024C>T (p.Asn1008=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.151680748G>C | CA348821022 | NEB | c.3024C>G (p.Asn1008Lys) | |
2 | g.151680748G= | CA1298292528 | NEB | c.3024C= (p.Asn1008=) | |
2 | g.151680748G>T | CA348821023 | NEB | c.3024C>A (p.Asn1008Lys) | |
2 | g.151680749T>A | CA348821024 | NEB | c.3023A>T (p.Asn1008Ile) | |
2 | g.151680749T>C | CA348821026 | NEB | c.3023A>G (p.Asn1008Ser) | |
2 | g.151680749T>G | CA348821025 | NEB | c.3023A>C (p.Asn1008Thr) | |
2 | g.151680750T>A | CA348821027 | NEB | c.3022A>T (p.Asn1008Tyr) | |
2 | g.151680750T>C | CA348821028 | NEB | c.3022A>G (p.Asn1008Asp) | ClinVar dbSNP gnomAD v4 |
2 | g.151680750T>G | CA348821029 | NEB | c.3022A>C (p.Asn1008His) | |
2 | g.151680750T= | CA1298292532 | NEB | c.3022A= (p.Asn1008=) | |
2 | g.151680751A>C | CA348821030 | NEB | c.3021T>G (p.Ile1007Met) | |
2 | g.151680751A>G | CA429243801 | NEB | c.3021T>C (p.Ile1007=) | |
2 | g.151680751A>T | CA429243800 | NEB | c.3021T>A (p.Ile1007=) |