Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.151680737C>ACA348820997NEBc.3035G>T (p.Arg1012Met)
2g.151680737C>GCA348820998NEBc.3035G>C (p.Arg1012Thr)
2g.151680737C>TCA348820999NEBc.3035G>A (p.Arg1012Lys)
2g.151680738T>ACA348821001NEBc.3034A>T (p.Arg1012Trp)
2g.151680738T>CCA348821000NEBc.3034A>G (p.Arg1012Gly)
2g.151680738T>GCA429243793NEBc.3034A>C (p.Arg1012=)
2g.151680739C>ACA348821002NEBc.3033G>T (p.Gln1011His)
2g.151680739C=CA1298292519NEBc.3033G= (p.Gln1011=)
2g.151680739C>GCA348821003NEBc.3033G>C (p.Gln1011His)
dbSNP gnomAD v4
2g.151680739C>TCA429243794NEBc.3033G>A (p.Gln1011=)
2g.151680740T>ACA348821004NEBc.3032A>T (p.Gln1011Leu)
2g.151680740T>CCA348821005NEBc.3032A>G (p.Gln1011Arg)
2g.151680740T>GCA348821006NEBc.3032A>C (p.Gln1011Pro)
2g.151680741G>ACA348821007NEBc.3031C>T (p.Gln1011Ter)
2g.151680741G>CCA348821008NEBc.3031C>G (p.Gln1011Glu)
2g.151680741G>TCA348821009NEBc.3031C>A (p.Gln1011Lys)
gnomAD v4
2g.151680742G>ACA429243795NEBc.3030C>T (p.Ala1010=)
2g.151680742G>CCA429243796NEBc.3030C>G (p.Ala1010=)
gnomAD v4
2g.151680742G>TCA429243797NEBc.3030C>A (p.Ala1010=)
ClinVar dbSNP
2g.151680743G>ACA1911041NEBc.3029C>T (p.Ala1010Val)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.151680743G>CCA348821010NEBc.3029C>G (p.Ala1010Gly)
gnomAD v4
2g.151680743G=CA1298292521NEBc.3029C= (p.Ala1010=)
2g.151680743G>TCA348821011NEBc.3029C>A (p.Ala1010Asp)
gnomAD v4
2g.151680744C>ACA348821012NEBc.3028G>T (p.Ala1010Ser)
dbSNP gnomAD v4
2g.151680744C=CA1298292525NEBc.3028G= (p.Ala1010=)
2g.151680744C>GCA348821013NEBc.3028G>C (p.Ala1010Pro)
ClinVar dbSNP
2g.151680744C>TCA1911042NEBc.3028G>A (p.Ala1010Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.151680745C>ACA348821015NEBc.3027G>T (p.Gln1009His)
2g.151680745C>GCA348821014NEBc.3027G>C (p.Gln1009His)
2g.151680745C>TCA429243798NEBc.3027G>A (p.Gln1009=)
ClinVar dbSNP gnomAD v4
2g.151680746T>ACA348821016NEBc.3026A>T (p.Gln1009Leu)
2g.151680746T>CCA348821017NEBc.3026A>G (p.Gln1009Arg)
gnomAD v4
2g.151680746T>GCA348821018NEBc.3026A>C (p.Gln1009Pro)
COSMIC COSMIC COSMIC
2g.151680747G>ACA348821019NEBc.3025C>T (p.Gln1009Ter)
ClinVar
2g.151680747G>CCA348821020NEBc.3025C>G (p.Gln1009Glu)
2g.151680747G>TCA348821021NEBc.3025C>A (p.Gln1009Lys)
gnomAD v4
2g.151680748G>ACA429243799NEBc.3024C>T (p.Asn1008=)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.151680748G>CCA348821022NEBc.3024C>G (p.Asn1008Lys)
2g.151680748G=CA1298292528NEBc.3024C= (p.Asn1008=)
2g.151680748G>TCA348821023NEBc.3024C>A (p.Asn1008Lys)
2g.151680749T>ACA348821024NEBc.3023A>T (p.Asn1008Ile)
2g.151680749T>CCA348821026NEBc.3023A>G (p.Asn1008Ser)
2g.151680749T>GCA348821025NEBc.3023A>C (p.Asn1008Thr)
2g.151680750T>ACA348821027NEBc.3022A>T (p.Asn1008Tyr)
2g.151680750T>CCA348821028NEBc.3022A>G (p.Asn1008Asp)
ClinVar dbSNP gnomAD v4
2g.151680750T>GCA348821029NEBc.3022A>C (p.Asn1008His)
2g.151680750T=CA1298292532NEBc.3022A= (p.Asn1008=)
2g.151680751A>CCA348821030NEBc.3021T>G (p.Ile1007Met)
2g.151680751A>GCA429243801NEBc.3021T>C (p.Ile1007=)
2g.151680751A>TCA429243800NEBc.3021T>A (p.Ile1007=)

Number of alleles fetched