Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.111119034G>ACA124932496WDR36c.1818G>A (p.Leu606=)
c.1986G>A (p.Leu662=)
dbSNP gnomAD v3 gnomAD v4
5g.111119034G>CCA360613478WDR36c.1818G>C (p.Leu606Phe)
c.1986G>C (p.Leu662Phe)
5g.111119034G=CA1572628327WDR36c.1818G= (p.Leu606=)
c.1986G= (p.Leu662=)
5g.111119034G>TCA360613477WDR36c.1818G>T (p.Leu606Phe)
c.1986G>T (p.Leu662Phe)
5g.111119035G>ACA360613481WDR36c.1819G>A (p.Asp607Asn)
c.1987G>A (p.Asp663Asn)
gnomAD v4
5g.111119035G>CCA360613479WDR36c.1819G>C (p.Asp607His)
c.1987G>C (p.Asp663His)
5g.111119035G>TCA360613480WDR36c.1819G>T (p.Asp607Tyr)
c.1987G>T (p.Asp663Tyr)
5g.111119036A>CCA360613482WDR36c.1820A>C (p.Asp607Ala)
c.1988A>C (p.Asp663Ala)
5g.111119036A>GCA360613483WDR36c.1820A>G (p.Asp607Gly)
c.1988A>G (p.Asp663Gly)
5g.111119036A>TCA360613484WDR36c.1820A>T (p.Asp607Val)
c.1988A>T (p.Asp663Val)
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)

Number of alleles fetched