Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.104034096A=CA1933418108COL17A1c.3759T= (p.Gly1253=)
c.35T=
c.4005T= (p.Gly1335=)
10g.104034096A>CCA471502779COL17A1c.3759T>G (p.Gly1253=)
c.35T>G
c.4005T>G (p.Gly1335=)
dbSNP
10g.104034096A>GCA471502777COL17A1c.3759T>C (p.Gly1253=)
c.35T>C
c.4005T>C (p.Gly1335=)
10g.104034096A>TCA471502778COL17A1c.3759T>A (p.Gly1253=)
c.35T>A
c.4005T>A (p.Gly1335=)
10g.104034096_104034097delinsACCA1933418106COL17A1c.3758_3759delinsGT (p.Gly1253=)
c.34_35delinsGT
c.4004_4005delinsGT (p.Gly1335=)
10g.104034097C>ACA378065196COL17A1c.3758G>T (p.Gly1253Val)
c.34G>T
c.4004G>T (p.Gly1335Val)
10g.104034097C=CA1933418112COL17A1c.3758G= (p.Gly1253=)
c.34G=
c.4004G= (p.Gly1335=)
10g.104034097C>GCA378065194COL17A1c.3758G>C (p.Gly1253Ala)
c.34G>C
c.4004G>C (p.Gly1335Ala)
10g.104034097C>TCA5677741COL17A1c.3758G>A (p.Gly1253Asp)
c.34G>A
c.4004G>A (p.Gly1335Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.104034100delCA1933418110COL17A1c.3758del (p.Gly1253ValfsTer?)
c.34del
c.4004del (p.Gly1335ValfsTer?)
dbSNP gnomAD v4
10g.104034098C>ACA378065198COL17A1c.3757G>T (p.Gly1253Cys)
c.33G>T
c.4003G>T (p.Gly1335Cys)
dbSNP gnomAD v4
10g.104034098C=CA1933418115COL17A1c.3757G= (p.Gly1253=)
c.33G=
c.4003G= (p.Gly1335=)
10g.104034098C>GCA378065199COL17A1c.3757G>C (p.Gly1253Arg)
c.33G>C
c.4003G>C (p.Gly1335Arg)
10g.104034098C>TCA378065201COL17A1c.3757G>A (p.Gly1253Ser)
c.33G>A
c.4003G>A (p.Gly1335Ser)
10g.104034099C>ACA378065203COL17A1c.3756G>T (p.Arg1252Ser)
c.32G>T
c.4002G>T (p.Arg1334Ser)
10g.104034099C=CA1933418118COL17A1c.3756G= (p.Arg1252=)
c.32G=
c.4002G= (p.Arg1334=)
10g.104034099C>GCA5677742COL17A1c.3756G>C (p.Arg1252Ser)
c.32G>C
c.4002G>C (p.Arg1334Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.104034099C>TCA471502782COL17A1c.3756G>A (p.Arg1252=)
c.32G>A
c.4002G>A (p.Arg1334=)
COSMIC
10g.104034099_104034101delinsCCTCA1933418119COL17A1c.3754_3756delinsAGG (p.Arg1252=)
c.30_32delinsAGG
c.4000_4002delinsAGG (p.Arg1334=)
10g.104034100C>ACA378065205COL17A1c.3755G>T (p.Arg1252Met)
c.31G>T
c.4001G>T (p.Arg1334Met)
10g.104034100C=CA1933418124COL17A1c.3755G= (p.Arg1252=)
c.31G=
c.4001G= (p.Arg1334=)
10g.104034100C>GCA378065207COL17A1c.3755G>C (p.Arg1252Thr)
c.31G>C
c.4001G>C (p.Arg1334Thr)
dbSNP gnomAD v2 gnomAD v4
10g.104034100C>TCA378065208COL17A1c.3755G>A (p.Arg1252Lys)
c.31G>A
c.4001G>A (p.Arg1334Lys)
10g.104034100_104034101delCA659193854COL17A1c.3754_3755del (p.Arg1252GlyfsTer6)
c.30_31del
c.4000_4001del (p.Arg1334GlyfsTer6)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.104034100_104034101delinsCTCA1933418122COL17A1c.3754_3755delinsAG (p.Arg1252=)
c.30_31delinsAG
c.4000_4001delinsAG (p.Arg1334=)
10g.104034101delCA5677743COL17A1c.3754del (p.Arg1252GlyfsTer?)
c.30del
c.4000del (p.Arg1334GlyfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.104034101T>ACA378065209COL17A1c.3754A>T (p.Arg1252Trp)
c.30A>T
c.4000A>T (p.Arg1334Trp)
10g.104034101T>CCA5677744COL17A1c.3754A>G (p.Arg1252Gly)
c.30A>G
c.4000A>G (p.Arg1334Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.104034101T>GCA471502786COL17A1c.3754A>C (p.Arg1252=)
c.30A>C
c.4000A>C (p.Arg1334=)
gnomAD v4
10g.104034101T=CA1933418130COL17A1c.3754A= (p.Arg1252=)
c.30A=
c.4000A= (p.Arg1334=)
10g.104034102G>ACA471502788COL17A1c.3753C>T (p.Asp1251=)
c.29C>T
c.3999C>T (p.Asp1333=)
10g.104034102G>CCA378065212COL17A1c.3753C>G (p.Asp1251Glu)
c.29C>G
c.3999C>G (p.Asp1333Glu)
10g.104034102G>TCA378065214COL17A1c.3753C>A (p.Asp1251Glu)
c.29C>A
c.3999C>A (p.Asp1333Glu)
10g.104034103T>ACA378065215COL17A1c.3752A>T (p.Asp1251Val)
c.28A>T
c.3998A>T (p.Asp1333Val)
10g.104034103T>CCA378065217COL17A1c.3752A>G (p.Asp1251Gly)
c.28A>G
c.3998A>G (p.Asp1333Gly)
10g.104034103T>GCA378065216COL17A1c.3752A>C (p.Asp1251Ala)
c.28A>C
c.3998A>C (p.Asp1333Ala)
10g.104034104C>ACA378065219COL17A1c.3751G>T (p.Asp1251Tyr)
c.27G>T
c.3997G>T (p.Asp1333Tyr)
10g.104034104C>GCA378065221COL17A1c.3751G>C (p.Asp1251His)
c.27G>C
c.3997G>C (p.Asp1333His)
10g.104034104C>TCA378065222COL17A1c.3751G>A (p.Asp1251Asn)
c.27G>A
c.3997G>A (p.Asp1333Asn)
dbSNP gnomAD v4
10g.104034105T>ACA471502791COL17A1c.3750A>T (p.Gly1250=)
c.26A>T
c.3996A>T (p.Gly1332=)
dbSNP
10g.104034105T>CCA471502792COL17A1c.3750A>G (p.Gly1250=)
c.26A>G
c.3996A>G (p.Gly1332=)
10g.104034105T>GCA471502794COL17A1c.3750A>C (p.Gly1250=)
c.26A>C
c.3996A>C (p.Gly1332=)
dbSNP gnomAD v2 gnomAD v4
10g.104034105T=CA1933418134COL17A1c.3750A= (p.Gly1250=)
c.26A=
c.3996A= (p.Gly1332=)
10g.104034106C>ACA378065223COL17A1c.3749G>T (p.Gly1250Val)
c.25G>T
c.3995G>T (p.Gly1332Val)
10g.104034106C=CA1933418138COL17A1c.3749G= (p.Gly1250=)
c.25G=
c.3995G= (p.Gly1332=)
10g.104034106C>GCA378065225COL17A1c.3749G>C (p.Gly1250Ala)
c.25G>C
c.3995G>C (p.Gly1332Ala)
dbSNP gnomAD v3 gnomAD v4
10g.104034106C>TCA378065227COL17A1c.3749G>A (p.Gly1250Glu)
c.25G>A
c.3995G>A (p.Gly1332Glu)
10g.104034107C>ACA378065228COL17A1c.3748G>T (p.Gly1250Ter)
c.24G>T
c.3994G>T (p.Gly1332Ter)
10g.104034107C=CA1933418142COL17A1c.3748G= (p.Gly1250=)
c.24G=
c.3994G= (p.Gly1332=)
10g.104034107C>GCA378065230COL17A1c.3748G>C (p.Gly1250Arg)
c.24G>C
c.3994G>C (p.Gly1332Arg)

Number of alleles fetched