Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.51806952C>ACA480062411SCN8Ac.5466C>A (p.Pro1822=)
c.3530C>A
c.5343C>A (p.Pro1781=)
c.5499C>A (p.Pro1833=)
12g.51806952C=CA2036194095SCN8Ac.5466C= (p.Pro1822=)
c.3530C=
c.5343C= (p.Pro1781=)
c.5499C= (p.Pro1833=)
12g.51806952C>GCA6571917SCN8Ac.5466C>G (p.Pro1822=)
c.3530C>G
c.5343C>G (p.Pro1781=)
c.5499C>G (p.Pro1833=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.51806952C>TCA6571918SCN8Ac.5466C>T (p.Pro1822=)
c.3530C>T
c.5343C>T (p.Pro1781=)
c.5499C>T (p.Pro1833=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.51806953A=CA2036194101SCN8Ac.5467A= (p.Lys1823=)
c.3531A=
c.5344A= (p.Lys1782=)
c.5500A= (p.Lys1834=)
12g.51806953A>CCA384886525SCN8Ac.5467A>C (p.Lys1823Gln)
c.3531A>C
c.5344A>C (p.Lys1782Gln)
c.5500A>C (p.Lys1834Gln)
12g.51806953A>GCA6571919SCN8Ac.5467A>G (p.Lys1823Glu)
c.3531A>G
c.5344A>G (p.Lys1782Glu)
c.5500A>G (p.Lys1834Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.51806953A>TCA384886529SCN8Ac.5467A>T (p.Lys1823Ter)
c.3531A>T
c.5344A>T (p.Lys1782Ter)
c.5500A>T (p.Lys1834Ter)
dbSNP
12g.51806954A>CCA384886535SCN8Ac.5468A>C (p.Lys1823Thr)
c.3532A>C
c.5345A>C (p.Lys1782Thr)
c.5501A>C (p.Lys1834Thr)
12g.51806954A>GCA384886539SCN8Ac.5468A>G (p.Lys1823Arg)
c.3532A>G
c.5345A>G (p.Lys1782Arg)
c.5501A>G (p.Lys1834Arg)
12g.51806954A>TCA384886540SCN8Ac.5468A>T (p.Lys1823Met)
c.3532A>T
c.5345A>T (p.Lys1782Met)
c.5501A>T (p.Lys1834Met)
12g.51806955G>ACA480062417SCN8Ac.5469G>A (p.Lys1823=)
c.3533G>A
c.5346G>A (p.Lys1782=)
c.5502G>A (p.Lys1834=)
gnomAD v4
12g.51806955G>CCA384886545SCN8Ac.5469G>C (p.Lys1823Asn)
c.3533G>C
c.5346G>C (p.Lys1782Asn)
c.5502G>C (p.Lys1834Asn)
12g.51806955G>TCA384886546SCN8Ac.5469G>T (p.Lys1823Asn)
c.3533G>T
c.5346G>T (p.Lys1782Asn)
c.5502G>T (p.Lys1834Asn)
12g.51806956C>ACA384886547SCN8Ac.5470C>A (p.Pro1824Thr)
c.3534C>A
c.5347C>A (p.Pro1783Thr)
c.5503C>A (p.Pro1835Thr)
12g.51806956C>GCA384886551SCN8Ac.5470C>G (p.Pro1824Ala)
c.3534C>G
c.5347C>G (p.Pro1783Ala)
c.5503C>G (p.Pro1835Ala)
12g.51806956C>TCA384886562SCN8Ac.5470C>T (p.Pro1824Ser)
c.3534C>T
c.5347C>T (p.Pro1783Ser)
c.5503C>T (p.Pro1835Ser)
12g.51806957C>ACA384886570SCN8Ac.5471C>A (p.Pro1824His)
c.3535C>A
c.5348C>A (p.Pro1783His)
c.5504C>A (p.Pro1835His)
12g.51806957C>GCA384886580SCN8Ac.5471C>G (p.Pro1824Arg)
c.3535C>G
c.5348C>G (p.Pro1783Arg)
c.5504C>G (p.Pro1835Arg)
12g.51806957C>TCA384886574SCN8Ac.5471C>T (p.Pro1824Leu)
c.3535C>T
c.5348C>T (p.Pro1783Leu)
c.5504C>T (p.Pro1835Leu)
12g.51806958C>ACA155097SCN8Ac.5472C>A (p.Pro1824=)
c.3536C>A
c.5349C>A (p.Pro1783=)
c.5505C>A (p.Pro1835=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.51806958C=CA2036194122SCN8Ac.5472C= (p.Pro1824=)
c.3536C=
c.5349C= (p.Pro1783=)
c.5505C= (p.Pro1835=)
12g.51806958C>GCA6571920SCN8Ac.5472C>G (p.Pro1824=)
c.3536C>G
c.5349C>G (p.Pro1783=)
c.5505C>G (p.Pro1835=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.51806958C>TCA236327655SCN8Ac.5472C>T (p.Pro1824=)
c.3536C>T
c.5349C>T (p.Pro1783=)
c.5505C>T (p.Pro1835=)
dbSNP
12g.51806958_51806959insTTTGCAGATGCCTTGGAGCATCCTCTCCGAGTGCCCAAGCCACA947652706SCN8Ac.5472_5473insTTTGCAGATGCCTTGGAGCATCCTCTCCGAGTGCCCAAGCCA (p.Pro1824_Asn1825insPheAlaAspAlaLeuGluHisProLeuArgValProLysPro)
c.3536_3537insTTTGCAGATGCCTTGGAGCATCCTCTCCGAGTGCCCAAGCCA
c.5349_5350insTTTGCAGATGCCTTGGAGCATCCTCTCCGAGTGCCCAAGCCA (p.Pro1783_Asn1784insPheAlaAspAlaLeuGluHisProLeuArgValProLysPro)
c.5505_5506insTTTGCAGATGCCTTGGAGCATCCTCTCCGAGTGCCCAAGCCA (p.Pro1835_Asn1836insPheAlaAspAlaLeuGluHisProLeuArgValProLysPro)
gnomAD v3 gnomAD v4
12g.51806959A>CCA384886591SCN8Ac.5473A>C (p.Asn1825His)
c.3537A>C
c.5350A>C (p.Asn1784His)
c.5506A>C (p.Asn1836His)
12g.51806959A>GCA384886593SCN8Ac.5473A>G (p.Asn1825Asp)
c.3537A>G
c.5350A>G (p.Asn1784Asp)
c.5506A>G (p.Asn1836Asp)
12g.51806959A>TCA384886604SCN8Ac.5473A>T (p.Asn1825Tyr)
c.3537A>T
c.5350A>T (p.Asn1784Tyr)
c.5506A>T (p.Asn1836Tyr)
12g.51806960A=CA2036194144SCN8Ac.5474A= (p.Asn1825=)
c.3538A=
c.5351A= (p.Asn1784=)
c.5507A= (p.Asn1836=)
12g.51806960A>CCA384886610SCN8Ac.5474A>C (p.Asn1825Thr)
c.3538A>C
c.5351A>C (p.Asn1784Thr)
c.5507A>C (p.Asn1836Thr)
12g.51806960A>GCA384886613SCN8Ac.5474A>G (p.Asn1825Ser)
c.3538A>G
c.5351A>G (p.Asn1784Ser)
c.5507A>G (p.Asn1836Ser)
dbSNP gnomAD v4
12g.51806960A>TCA384886612SCN8Ac.5474A>T (p.Asn1825Ile)
c.3538A>T
c.5351A>T (p.Asn1784Ile)
c.5507A>T (p.Asn1836Ile)
12g.51806961T>ACA384886617SCN8Ac.5475T>A (p.Asn1825Lys)
c.3539T>A
c.5352T>A (p.Asn1784Lys)
c.5508T>A (p.Asn1836Lys)
dbSNP
12g.51806961T>CCA6571921SCN8Ac.5475T>C (p.Asn1825=)
c.3539T>C
c.5352T>C (p.Asn1784=)
c.5508T>C (p.Asn1836=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.51806961T>GCA384886618SCN8Ac.5475T>G (p.Asn1825Lys)
c.3539T>G
c.5352T>G (p.Asn1784Lys)
c.5508T>G (p.Asn1836Lys)
12g.51806961T=CA2036194153SCN8Ac.5475T= (p.Asn1825=)
c.3539T=
c.5352T= (p.Asn1784=)
c.5508T= (p.Asn1836=)
12g.51806962A>CCA384886623SCN8Ac.5476A>C (p.Thr1826Pro)
c.3540A>C
c.5353A>C (p.Thr1785Pro)
c.5509A>C (p.Thr1837Pro)
12g.51806962A>GCA384886628SCN8Ac.5476A>G (p.Thr1826Ala)
c.3540A>G
c.5353A>G (p.Thr1785Ala)
c.5509A>G (p.Thr1837Ala)
gnomAD v4
12g.51806962A>TCA384886635SCN8Ac.5476A>T (p.Thr1826Ser)
c.3540A>T
c.5353A>T (p.Thr1785Ser)
c.5509A>T (p.Thr1837Ser)
12g.51806963C>ACA384886636SCN8Ac.5477C>A (p.Thr1826Asn)
c.3541C>A
c.5354C>A (p.Thr1785Asn)
c.5510C>A (p.Thr1837Asn)
12g.51806963C>GCA384886637SCN8Ac.5477C>G (p.Thr1826Ser)
c.3541C>G
c.5354C>G (p.Thr1785Ser)
c.5510C>G (p.Thr1837Ser)
gnomAD v4
12g.51806963C>TCA384886638SCN8Ac.5477C>T (p.Thr1826Ile)
c.3541C>T
c.5354C>T (p.Thr1785Ile)
c.5510C>T (p.Thr1837Ile)
12g.51806964C>ACA480061857SCN8Ac.5478C>A (p.Thr1826=)
c.3542C>A
c.5355C>A (p.Thr1785=)
c.5511C>A (p.Thr1837=)
12g.51806964C>GCA480061858SCN8Ac.5478C>G (p.Thr1826=)
c.3542C>G
c.5355C>G (p.Thr1785=)
c.5511C>G (p.Thr1837=)
12g.51806964C>TCA480061859SCN8Ac.5478C>T (p.Thr1826=)
c.3542C>T
c.5355C>T (p.Thr1785=)
c.5511C>T (p.Thr1837=)
gnomAD v4
12g.51806965A=CA2036194160SCN8Ac.5479A= (p.Ile1827=)
c.3543A=
c.5356A= (p.Ile1786=)
c.5512A= (p.Ile1838=)
12g.51806965A>CCA384886640SCN8Ac.5479A>C (p.Ile1827Leu)
c.3543A>C
c.5356A>C (p.Ile1786Leu)
c.5512A>C (p.Ile1838Leu)
12g.51806965A>GCA6571922SCN8Ac.5479A>G (p.Ile1827Val)
c.3543A>G
c.5356A>G (p.Ile1786Val)
c.5512A>G (p.Ile1838Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.51806965A>TCA384886643SCN8Ac.5479A>T (p.Ile1827Phe)
c.3543A>T
c.5356A>T (p.Ile1786Phe)
c.5512A>T (p.Ile1838Phe)
12g.51806966T>ACA384886650SCN8Ac.5480T>A (p.Ile1827Asn)
c.3544T>A
c.5357T>A (p.Ile1786Asn)
c.5513T>A (p.Ile1838Asn)

Number of alleles fetched