Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.104064484G>ACA471338819COL17A1c.720C>T (p.Thr240=)
n.835C>T
c.672C>T (p.Thr224=)
n.65C>T
gnomAD v4
10g.104064484G>CCA471338821COL17A1c.720C>G (p.Thr240=)
n.835C>G
c.672C>G (p.Thr224=)
n.65C>G
10g.104064484G>TCA471338820COL17A1c.720C>A (p.Thr240=)
n.835C>A
c.672C>A (p.Thr224=)
n.65C>A
10g.104064485G>ACA5679322COL17A1c.719C>T (p.Thr240Ile)
n.834C>T
c.671C>T (p.Thr224Ile)
n.64C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.104064485G>CCA378077282COL17A1c.719C>G (p.Thr240Ser)
n.834C>G
c.671C>G (p.Thr224Ser)
n.64C>G
10g.104064485G=CA1933374485COL17A1c.719C= (p.Thr240=)
n.834C=
c.671C= (p.Thr224=)
n.64C=
10g.104064485G>TCA378077284COL17A1c.719C>A (p.Thr240Asn)
n.834C>A
c.671C>A (p.Thr224Asn)
n.64C>A
gnomAD v4
10g.104064486T>ACA378077287COL17A1c.718A>T (p.Thr240Ser)
n.833A>T
c.670A>T (p.Thr224Ser)
n.63A>T
10g.104064486T>CCA378077288COL17A1c.718A>G (p.Thr240Ala)
n.833A>G
c.670A>G (p.Thr224Ala)
n.63A>G
10g.104064486T>GCA378077290COL17A1c.718A>C (p.Thr240Pro)
n.833A>C
c.670A>C (p.Thr224Pro)
n.63A>C
10g.104064487delCA2695212701COL17A1c.718del (p.Thr240ProfsTer?)
n.833del
c.670del (p.Thr224ProfsTer?)
n.63del
10g.104064487T>ACA471338822COL17A1c.717A>T (p.Thr239=)
n.832A>T
c.669A>T (p.Thr223=)
n.62A>T
10g.104064487T>CCA471338823COL17A1c.717A>G (p.Thr239=)
n.832A>G
c.669A>G (p.Thr223=)
n.62A>G
10g.104064487T>GCA471338824COL17A1c.717A>C (p.Thr239=)
n.832A>C
c.669A>C (p.Thr223=)
n.62A>C
10g.104064488G>ACA378077294COL17A1c.716C>T (p.Thr239Ile)
n.831C>T
c.668C>T (p.Thr223Ile)
n.61C>T
10g.104064488G>CCA378077293COL17A1c.716C>G (p.Thr239Arg)
n.831C>G
c.668C>G (p.Thr223Arg)
n.61C>G
10g.104064488G>TCA378077292COL17A1c.716C>A (p.Thr239Lys)
n.831C>A
c.668C>A (p.Thr223Lys)
n.61C>A
gnomAD v4
10g.104064489T>ACA378077296COL17A1c.715A>T (p.Thr239Ser)
n.830A>T
c.667A>T (p.Thr223Ser)
n.60A>T
gnomAD v4
10g.104064489T>CCA378077298COL17A1c.715A>G (p.Thr239Ala)
n.830A>G
c.667A>G (p.Thr223Ala)
n.60A>G
10g.104064489T>GCA378077300COL17A1c.715A>C (p.Thr239Pro)
n.830A>C
c.667A>C (p.Thr223Pro)
n.60A>C
10g.104064490C>ACA378077301COL17A1c.714G>T (p.Met238Ile)
n.829G>T
c.666G>T (p.Met222Ile)
n.59G>T
10g.104064490C=CA1933374486COL17A1c.714G= (p.Met238=)
n.829G=
c.666G= (p.Met222=)
n.59G=
10g.104064490C>GCA378077303COL17A1c.714G>C (p.Met238Ile)
n.829G>C
c.666G>C (p.Met222Ile)
n.59G>C
10g.104064490C>TCA212425512COL17A1c.714G>A (p.Met238Ile)
n.829G>A
c.666G>A (p.Met222Ile)
n.59G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.104064490_104064491insGCCGTCA2559023116COL17A1c.713_714insACGGC (p.Met238IlefsTer?)
n.828_829insACGGC
c.665_666insACGGC (p.Met222IlefsTer?)
n.58_59insACGGC
10g.104064491A>CCA378077304COL17A1c.713T>G (p.Met238Arg)
n.828T>G
c.665T>G (p.Met222Arg)
n.58T>G
10g.104064491A>GCA378077308COL17A1c.713T>C (p.Met238Thr)
n.828T>C
c.665T>C (p.Met222Thr)
n.58T>C
10g.104064491A>TCA378077306COL17A1c.713T>A (p.Met238Lys)
n.828T>A
c.665T>A (p.Met222Lys)
n.58T>A
10g.104064492T>ACA378077309COL17A1c.712A>T (p.Met238Leu)
n.827A>T
c.664A>T (p.Met222Leu)
n.57A>T
10g.104064492T>CCA378077310COL17A1c.712A>G (p.Met238Val)
n.827A>G
c.664A>G (p.Met222Val)
n.57A>G
10g.104064492T>GCA5679323COL17A1c.712A>C (p.Met238Leu)
n.827A>C
c.664A>C (p.Met222Leu)
n.57A>C
dbSNP ExAC gnomAD v2 gnomAD v4
10g.104064492T=CA1933374487COL17A1c.712A= (p.Met238=)
n.827A=
c.664A= (p.Met222=)
n.57A=
10g.104064498_104064500delCA2610805434COL17A1c.710_712del (p.Asn237del)
n.825_827del
c.662_664del (p.Asn221del)
n.55_57del
gnomAD v4
10g.104064492_104064493insCCA2546263780COL17A1c.711_712insG (p.Met238AspfsTer?)
n.826_827insG
c.663_664insG (p.Met222AspfsTer?)
n.56_57insG
10g.104064493G>ACA471338825COL17A1c.711C>T (p.Asn237=)
n.826C>T
c.663C>T (p.Asn221=)
n.56C>T
ClinVar gnomAD v4
10g.104064493G>CCA378077312COL17A1c.711C>G (p.Asn237Lys)
n.826C>G
c.663C>G (p.Asn221Lys)
n.56C>G
10g.104064493G>TCA378077314COL17A1c.711C>A (p.Asn237Lys)
n.826C>A
c.663C>A (p.Asn221Lys)
n.56C>A
10g.104064494T>ACA378077316COL17A1c.710A>T (p.Asn237Ile)
n.825A>T
c.662A>T (p.Asn221Ile)
n.55A>T
10g.104064494T>CCA212425516COL17A1c.710A>G (p.Asn237Ser)
n.825A>G
c.662A>G (p.Asn221Ser)
n.55A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.104064494T>GCA378077317COL17A1c.710A>C (p.Asn237Thr)
n.825A>C
c.662A>C (p.Asn221Thr)
n.55A>C
10g.104064494T=CA1933374488COL17A1c.710A= (p.Asn237=)
n.825A=
c.662A= (p.Asn221=)
n.55A=
10g.104064495T>ACA378077320COL17A1c.709A>T (p.Asn237Tyr)
n.824A>T
c.661A>T (p.Asn221Tyr)
n.54A>T
10g.104064495T>CCA378077321COL17A1c.709A>G (p.Asn237Asp)
n.824A>G
c.661A>G (p.Asn221Asp)
n.54A>G
dbSNP gnomAD v2
10g.104064495T>GCA378077323COL17A1c.709A>C (p.Asn237His)
n.824A>C
c.661A>C (p.Asn221His)
n.54A>C
10g.104064495T=CA1933374489COL17A1c.709A= (p.Asn237=)
n.824A=
c.661A= (p.Asn221=)
n.54A=
10g.104064495_104064496insAAAAAACA2571109654COL17A1c.708_709insTTTTTT (p.Asn236_Asn237insPhePhe)
n.823_824insTTTTTT
c.660_661insTTTTTT (p.Asn220_Asn221insPhePhe)
n.53_54insTTTTTT
10g.104064496G>ACA5679325COL17A1c.708C>T (p.Asn236=)
n.823C>T
c.660C>T (p.Asn220=)
n.53C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.104064496G>CCA378077326COL17A1c.708C>G (p.Asn236Lys)
n.823C>G
c.660C>G (p.Asn220Lys)
n.53C>G
10g.104064496G=CA1933374490COL17A1c.708C= (p.Asn236=)
n.823C=
c.660C= (p.Asn220=)
n.53C=
10g.104064496G>TCA5679324COL17A1c.708C>A (p.Asn236Lys)
n.823C>A
c.660C>A (p.Asn220Lys)
n.53C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched