Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.125434322A=CA1491646818FAT4c.7096A= (p.Ser2366=)
c.1867A= (p.Ser623=)
c.1990A= (p.Ser664=)
4g.125434322A>CCA358135199FAT4c.7096A>C (p.Ser2366Arg)
c.1867A>C (p.Ser623Arg)
c.1990A>C (p.Ser664Arg)
 dbSNP
4g.125434322A>GCA358135196FAT4c.7096A>G (p.Ser2366Gly)
c.1867A>G (p.Ser623Gly)
c.1990A>G (p.Ser664Gly)
4g.125434322A>TCA358135198FAT4c.7096A>T (p.Ser2366Cys)
c.1867A>T (p.Ser623Cys)
c.1990A>T (p.Ser664Cys)
 gnomAD v4
4g.125434323G>ACA358135201FAT4c.7097G>A (p.Ser2366Asn)
c.1868G>A (p.Ser623Asn)
c.1991G>A (p.Ser664Asn)
4g.125434323G>CCA358135203FAT4c.7097G>C (p.Ser2366Thr)
c.1868G>C (p.Ser623Thr)
c.1991G>C (p.Ser664Thr)
4g.125434323G>TCA358135204FAT4c.7097G>T (p.Ser2366Ile)
c.1868G>T (p.Ser623Ile)
c.1991G>T (p.Ser664Ile)
 COSMIC COSMIC
4g.125434324T>ACA358135205FAT4c.7098T>A (p.Ser2366Arg)
c.1869T>A (p.Ser623Arg)
c.1992T>A (p.Ser664Arg)
4g.125434324T>CCA3073093FAT4c.7098T>C (p.Ser2366=)
c.1869T>C (p.Ser623=)
c.1992T>C (p.Ser664=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.125434324T>GCA358135207FAT4c.7098T>G (p.Ser2366Arg)
c.1869T>G (p.Ser623Arg)
c.1992T>G (p.Ser664Arg)
4g.125434324T=CA1491646819FAT4c.7098T= (p.Ser2366=)
c.1869T= (p.Ser623=)
c.1992T= (p.Ser664=)
4g.125434325A=CA1491646820FAT4c.7099A= (p.Lys2367=)
c.1870A= (p.Lys624=)
c.1993A= (p.Lys665=)
4g.125434325A>CCA358135209FAT4c.7099A>C (p.Lys2367Gln)
c.1870A>C (p.Lys624Gln)
c.1993A>C (p.Lys665Gln)
4g.125434325A>GCA358135211FAT4c.7099A>G (p.Lys2367Glu)
c.1870A>G (p.Lys624Glu)
c.1993A>G (p.Lys665Glu)
 dbSNP gnomAD v4 COSMIC
4g.125434325A>TCA358135212FAT4c.7099A>T (p.Lys2367Ter)
c.1870A>T (p.Lys624Ter)
c.1993A>T (p.Lys665Ter)
4g.125434326A>CCA358135213FAT4c.7100A>C (p.Lys2367Thr)
c.1871A>C (p.Lys624Thr)
c.1994A>C (p.Lys665Thr)
4g.125434326A>GCA358135215FAT4c.7100A>G (p.Lys2367Arg)
c.1871A>G (p.Lys624Arg)
c.1994A>G (p.Lys665Arg)
4g.125434326A>TCA358135217FAT4c.7100A>T (p.Lys2367Ile)
c.1871A>T (p.Lys624Ile)
c.1994A>T (p.Lys665Ile)
4g.125434327A=CA1491646821FAT4c.7101A= (p.Lys2367=)
c.1872A= (p.Lys624=)
c.1995A= (p.Lys665=)
4g.125434327A>CCA358135218FAT4c.7101A>C (p.Lys2367Asn)
c.1872A>C (p.Lys624Asn)
c.1995A>C (p.Lys665Asn)
4g.125434327A>GCA441205018FAT4c.7101A>G (p.Lys2367=)
c.1872A>G (p.Lys624=)
c.1995A>G (p.Lys665=)
 dbSNP gnomAD v2 gnomAD v4
4g.125434327A>TCA358135220FAT4c.7101A>T (p.Lys2367Asn)
c.1872A>T (p.Lys624Asn)
c.1995A>T (p.Lys665Asn)
4g.125434328G>ACA358135221FAT4c.7102G>A (p.Ala2368Thr)
c.1873G>A (p.Ala625Thr)
c.1996G>A (p.Ala666Thr)
4g.125434328G>CCA358135222FAT4c.7102G>C (p.Ala2368Pro)
c.1873G>C (p.Ala625Pro)
c.1996G>C (p.Ala666Pro)
4g.125434328G>TCA358135223FAT4c.7102G>T (p.Ala2368Ser)
c.1873G>T (p.Ala625Ser)
c.1996G>T (p.Ala666Ser)
4g.125434329C>ACA3073094FAT4c.7103C>A (p.Ala2368Glu)
c.1874C>A (p.Ala625Glu)
c.1997C>A (p.Ala666Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125434329C=CA1491646822FAT4c.7103C= (p.Ala2368=)
c.1874C= (p.Ala625=)
c.1997C= (p.Ala666=)
4g.125434329C>GCA358135226FAT4c.7103C>G (p.Ala2368Gly)
c.1874C>G (p.Ala625Gly)
c.1997C>G (p.Ala666Gly)
4g.125434329C>TCA358135228FAT4c.7103C>T (p.Ala2368Val)
c.1874C>T (p.Ala625Val)
c.1997C>T (p.Ala666Val)
 ClinVar dbSNP gnomAD v4
4g.125434330G>ACA3073095FAT4c.7104G>A (p.Ala2368=)
c.1875G>A (p.Ala625=)
c.1998G>A (p.Ala666=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
4g.125434330G>CCA441205019FAT4c.7104G>C (p.Ala2368=)
c.1875G>C (p.Ala625=)
c.1998G>C (p.Ala666=)
4g.125434330G=CA1491646823FAT4c.7104G= (p.Ala2368=)
c.1875G= (p.Ala625=)
c.1998G= (p.Ala666=)
4g.125434330G>TCA441205020FAT4c.7104G>T (p.Ala2368=)
c.1875G>T (p.Ala625=)
c.1998G>T (p.Ala666=)
4g.125434331T>ACA358135230FAT4c.7105T>A (p.Tyr2369Asn)
c.1876T>A (p.Tyr626Asn)
c.1999T>A (p.Tyr667Asn)
4g.125434331T>CCA358135231FAT4c.7105T>C (p.Tyr2369His)
c.1876T>C (p.Tyr626His)
c.1999T>C (p.Tyr667His)
4g.125434331T>GCA358135232FAT4c.7105T>G (p.Tyr2369Asp)
c.1876T>G (p.Tyr626Asp)
c.1999T>G (p.Tyr667Asp)
4g.125434332A=CA1491646824FAT4c.7106A= (p.Tyr2369=)
c.1877A= (p.Tyr626=)
c.2000A= (p.Tyr667=)
4g.125434332A>CCA358135234FAT4c.7106A>C (p.Tyr2369Ser)
c.1877A>C (p.Tyr626Ser)
c.2000A>C (p.Tyr667Ser)
4g.125434332A>GCA3073096FAT4c.7106A>G (p.Tyr2369Cys)
c.1877A>G (p.Tyr626Cys)
c.2000A>G (p.Tyr667Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125434332A>TCA358135235FAT4c.7106A>T (p.Tyr2369Phe)
c.1877A>T (p.Tyr626Phe)
c.2000A>T (p.Tyr667Phe)
4g.125434333T>ACA358135238FAT4c.7107T>A (p.Tyr2369Ter)
c.1878T>A (p.Tyr626Ter)
c.2001T>A (p.Tyr667Ter)
4g.125434333T>CCA441205021FAT4c.7107T>C (p.Tyr2369=)
c.1878T>C (p.Tyr626=)
c.2001T>C (p.Tyr667=)
4g.125434333T>GCA358135237FAT4c.7107T>G (p.Tyr2369Ter)
c.1878T>G (p.Tyr626Ter)
c.2001T>G (p.Tyr667Ter)
4g.125434334T>ACA358135240FAT4c.7108T>A (p.Phe2370Ile)
c.1879T>A (p.Phe627Ile)
c.2002T>A (p.Phe668Ile)
4g.125434334T>CCA358135241FAT4c.7108T>C (p.Phe2370Leu)
c.1879T>C (p.Phe627Leu)
c.2002T>C (p.Phe668Leu)
4g.125434334T>GCA358135243FAT4c.7108T>G (p.Phe2370Val)
c.1879T>G (p.Phe627Val)
c.2002T>G (p.Phe668Val)
4g.125434335T>ACA358135245FAT4c.7109T>A (p.Phe2370Tyr)
c.1880T>A (p.Phe627Tyr)
c.2003T>A (p.Phe668Tyr)
4g.125434335T>CCA358135246FAT4c.7109T>C (p.Phe2370Ser)
c.1880T>C (p.Phe627Ser)
c.2003T>C (p.Phe668Ser)
4g.125434335T>GCA358135247FAT4c.7109T>G (p.Phe2370Cys)
c.1880T>G (p.Phe627Cys)
c.2003T>G (p.Phe668Cys)
 dbSNP gnomAD v2 gnomAD v4
4g.125434335T=CA1491646825FAT4c.7109T= (p.Phe2370=)
c.1880T= (p.Phe627=)
c.2003T= (p.Phe668=)

Number of alleles fetched