Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.151672460_151672481delCA2549819954NEBc.4188_4209del (p.Gln1397ThrfsTer16)
2g.151672462A=CA1298291106NEBc.4206T= (p.Asn1402=)
2g.151672462A>CCA348816568NEBc.4206T>G (p.Asn1402Lys)
2g.151672462A>GCA429453469NEBc.4206T>C (p.Asn1402=)
ClinVar gnomAD v4
2g.151672462A>TCA1910700NEBc.4206T>A (p.Asn1402Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.151672463T>ACA348816570NEBc.4205A>T (p.Asn1402Ile)
2g.151672463T>CCA348816571NEBc.4205A>G (p.Asn1402Ser)
gnomAD v4
2g.151672463T>GCA348816569NEBc.4205A>C (p.Asn1402Thr)
2g.151672464T>ACA348816573NEBc.4204A>T (p.Asn1402Tyr)
2g.151672464T>CCA348816572NEBc.4204A>G (p.Asn1402Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.151672464T>GCA348816574NEBc.4204A>C (p.Asn1402His)
2g.151672464T=CA1298291113NEBc.4204A= (p.Asn1402=)
2g.151672465G>ACA429453470NEBc.4203C>T (p.Thr1401=)
dbSNP gnomAD v2 gnomAD v4
2g.151672465G>CCA429453471NEBc.4203C>G (p.Thr1401=)
2g.151672465G=CA1298291118NEBc.4203C= (p.Thr1401=)
2g.151672465G>TCA429453472NEBc.4203C>A (p.Thr1401=)
gnomAD v4
2g.151672466G>ACA348816575NEBc.4202C>T (p.Thr1401Ile)
2g.151672466G>CCA348816576NEBc.4202C>G (p.Thr1401Ser)
2g.151672466G>TCA348816577NEBc.4202C>A (p.Thr1401Asn)
2g.151672467T>ACA348816578NEBc.4201A>T (p.Thr1401Ser)
2g.151672467T>CCA348816579NEBc.4201A>G (p.Thr1401Ala)
2g.151672467T>GCA348816580NEBc.4201A>C (p.Thr1401Pro)
2g.151672468A>CCA429453475NEBc.4200T>G (p.Ala1400=)
2g.151672468A>GCA429453474NEBc.4200T>C (p.Ala1400=)
2g.151672468A>TCA429453473NEBc.4200T>A (p.Ala1400=)
gnomAD v4
2g.151672469G>ACA348816581NEBc.4199C>T (p.Ala1400Val)
2g.151672469G>CCA348816582NEBc.4199C>G (p.Ala1400Gly)
gnomAD v4
2g.151672469G>TCA348816583NEBc.4199C>A (p.Ala1400Asp)
2g.151672470C>ACA348816584NEBc.4198G>T (p.Ala1400Ser)
gnomAD v4
2g.151672470C=CA1298291125NEBc.4198G= (p.Ala1400=)
2g.151672470C>GCA348816585NEBc.4198G>C (p.Ala1400Pro)
2g.151672470C>TCA358031NEBc.4198G>A (p.Ala1400Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.151672471G>ACA1910701NEBc.4197C>T (p.Val1399=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
2g.151672471G>CCA429453476NEBc.4197C>G (p.Val1399=)
2g.151672471G=CA1298291134NEBc.4197C= (p.Val1399=)
2g.151672471G>TCA429453477NEBc.4197C>A (p.Val1399=)
2g.151672472A=CA1298291140NEBc.4196T= (p.Val1399=)
2g.151672472A>CCA348816586NEBc.4196T>G (p.Val1399Gly)
2g.151672472A>GCA348816588NEBc.4196T>C (p.Val1399Ala)
gnomAD v4
2g.151672472A>TCA348816587NEBc.4196T>A (p.Val1399Asp)
dbSNP gnomAD v2 gnomAD v4
2g.151672473C>ACA348816589NEBc.4195G>T (p.Val1399Phe)
2g.151672473C>GCA348816590NEBc.4195G>C (p.Val1399Leu)
2g.151672473C>TCA348816591NEBc.4195G>A (p.Val1399Ile)
gnomAD v4
2g.151672474A>CCA348816592NEBc.4194T>G (p.Asp1398Glu)
2g.151672474A>GCA429453478NEBc.4194T>C (p.Asp1398=)
2g.151672474A>TCA348816593NEBc.4194T>A (p.Asp1398Glu)
2g.151672475T>ACA348816594NEBc.4193A>T (p.Asp1398Val)
gnomAD v4
2g.151672475T>CCA348816595NEBc.4193A>G (p.Asp1398Gly)
dbSNP gnomAD v4
2g.151672475T>GCA348816596NEBc.4193A>C (p.Asp1398Ala)
2g.151672475T=CA1298291144NEBc.4193A= (p.Asp1398=)

Number of alleles fetched