Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.111119037C>ACA360613485WDR36c.1821C>A (p.Asp607Glu)
c.1989C>A (p.Asp663Glu)
5g.111119037C>GCA360613486WDR36c.1821C>G (p.Asp607Glu)
c.1989C>G (p.Asp663Glu)
5g.111119037C>TCA445744822WDR36c.1821C>T (p.Asp607=)
c.1989C>T (p.Asp663=)
5g.111119038T>ACA360613487WDR36c.1822T>A (p.Ser608Thr)
c.1990T>A (p.Ser664Thr)
5g.111119038T>CCA360613489WDR36c.1822T>C (p.Ser608Pro)
c.1990T>C (p.Ser664Pro)
5g.111119038T>GCA360613488WDR36c.1822T>G (p.Ser608Ala)
c.1990T>G (p.Ser664Ala)
5g.111119039C>ACA360613490WDR36c.1823C>A (p.Ser608Ter)
c.1991C>A (p.Ser664Ter)
5g.111119039C=CA1572628328WDR36c.1823C= (p.Ser608=)
c.1991C= (p.Ser664=)
5g.111119039C>GCA360613491WDR36c.1823C>G (p.Ser608Trp)
c.1991C>G (p.Ser664Trp)
dbSNP gnomAD v2 gnomAD v4
5g.111119039C>TCA3365884WDR36c.1823C>T (p.Ser608Leu)
c.1991C>T (p.Ser664Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.111119040G>ACA3365885WDR36c.1824G>A (p.Ser608=)
c.1992G>A (p.Ser664=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
5g.111119040G>CCA445744823WDR36c.1824G>C (p.Ser608=)
c.1992G>C (p.Ser664=)
5g.111119040G=CA1572628329WDR36c.1824G= (p.Ser608=)
c.1992G= (p.Ser664=)
5g.111119040G>TCA445744824WDR36c.1824G>T (p.Ser608=)
c.1992G>T (p.Ser664=)
gnomAD v4
5g.111119041G>ACA360613492WDR36c.1825G>A (p.Ala609Thr)
c.1993G>A (p.Ala665Thr)
5g.111119041G>CCA360613494WDR36c.1825G>C (p.Ala609Pro)
c.1993G>C (p.Ala665Pro)
5g.111119041G>TCA360613493WDR36c.1825G>T (p.Ala609Ser)
c.1993G>T (p.Ala665Ser)
5g.111119042C>ACA360613495WDR36c.1826C>A (p.Ala609Asp)
c.1994C>A (p.Ala665Asp)
5g.111119042C=CA1572628330WDR36c.1826C= (p.Ala609=)
c.1994C= (p.Ala665=)
5g.111119042C>GCA360613496WDR36c.1826C>G (p.Ala609Gly)
c.1994C>G (p.Ala665Gly)
5g.111119042C>TCA124932505WDR36c.1826C>T (p.Ala609Val)
c.1994C>T (p.Ala665Val)
dbSNP gnomAD v4
5g.111119043T>ACA445744825WDR36c.1827T>A (p.Ala609=)
c.1995T>A (p.Ala665=)
gnomAD v4
5g.111119043T>CCA445744826WDR36c.1827T>C (p.Ala609=)
c.1995T>C (p.Ala665=)
5g.111119043T>GCA445744827WDR36c.1827T>G (p.Ala609=)
c.1995T>G (p.Ala665=)
5g.111119044C>ACA360613497WDR36c.1828C>A (p.Pro610Thr)
c.1996C>A (p.Pro666Thr)
5g.111119044C=CA1572628331WDR36c.1828C= (p.Pro610=)
c.1996C= (p.Pro666=)
5g.111119044C>GCA360613498WDR36c.1828C>G (p.Pro610Ala)
c.1996C>G (p.Pro666Ala)
gnomAD v4
5g.111119044C>TCA360613499WDR36c.1828C>T (p.Pro610Ser)
c.1996C>T (p.Pro666Ser)
dbSNP gnomAD v2 gnomAD v4 COSMIC
5g.111119045delCA2674832895WDR36c.1829del (p.Pro610LeufsTer?)
c.1997del (p.Pro666LeufsTer?)
gnomAD v4
5g.111119045C>ACA360613500WDR36c.1829C>A (p.Pro610His)
c.1997C>A (p.Pro666His)
5g.111119045C>GCA360613501WDR36c.1829C>G (p.Pro610Arg)
c.1997C>G (p.Pro666Arg)
5g.111119045C>TCA360613502WDR36c.1829C>T (p.Pro610Leu)
c.1997C>T (p.Pro666Leu)
5g.111119048_111119049delCA2674832896WDR36c.1832_1833del (p.Leu611GlnfsTer?)
c.2000_2001del (p.Leu667GlnfsTer?)
gnomAD v4
5g.111119046T>ACA445744828WDR36c.1830T>A (p.Pro610=)
c.1998T>A (p.Pro666=)
5g.111119046T>CCA445744829WDR36c.1830T>C (p.Pro610=)
c.1998T>C (p.Pro666=)
5g.111119046T>GCA445744830WDR36c.1830T>G (p.Pro610=)
c.1998T>G (p.Pro666=)
5g.111119047C>ACA360613503WDR36c.1831C>A (p.Leu611Ile)
c.1999C>A (p.Leu667Ile)
5g.111119047C>GCA360613504WDR36c.1831C>G (p.Leu611Val)
c.1999C>G (p.Leu667Val)
5g.111119047C>TCA360613505WDR36c.1831C>T (p.Leu611Phe)
c.1999C>T (p.Leu667Phe)
5g.111119048T>ACA360613507WDR36c.1832T>A (p.Leu611His)
c.2000T>A (p.Leu667His)
5g.111119048T>CCA360613508WDR36c.1832T>C (p.Leu611Pro)
c.2000T>C (p.Leu667Pro)
5g.111119048T>GCA360613506WDR36c.1832T>G (p.Leu611Arg)
c.2000T>G (p.Leu667Arg)
5g.111119049C>ACA445744831WDR36c.1833C>A (p.Leu611=)
c.2001C>A (p.Leu667=)
5g.111119049C>GCA445744832WDR36c.1833C>G (p.Leu611=)
c.2001C>G (p.Leu667=)
5g.111119049C>TCA445744833WDR36c.1833C>T (p.Leu611=)
c.2001C>T (p.Leu667=)
gnomAD v4
5g.111119050A=CA1572628332WDR36c.1834A= (p.Asn612=)
c.2002A= (p.Asn668=)
5g.111119050A>CCA360613509WDR36c.1834A>C (p.Asn612His)
c.2002A>C (p.Asn668His)
dbSNP gnomAD v2 gnomAD v4
5g.111119050A>GCA360613511WDR36c.1834A>G (p.Asn612Asp)
c.2002A>G (p.Asn668Asp)
5g.111119050A>TCA360613510WDR36c.1834A>T (p.Asn612Tyr)
c.2002A>T (p.Asn668Tyr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.111119051A=CA1572628333WDR36c.1835A= (p.Asn612=)
c.2003A= (p.Asn668=)

Number of alleles fetched