Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.108753476A=CA1278286974RANBP2c.1968A= (p.Ile656=)
c.1890A= (p.Ile630=)
c.1965A= (p.Ile655=)
2g.108753476A>CCA427909886RANBP2c.1968A>C (p.Ile656=)
c.1890A>C (p.Ile630=)
c.1965A>C (p.Ile655=)
2g.108753476A>GCA1822499RANBP2c.1968A>G (p.Ile656Met)
c.1890A>G (p.Ile630Met)
c.1965A>G (p.Ile655Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.108753476A>TCA427909887RANBP2c.1968A>T (p.Ile656=)
c.1890A>T (p.Ile630=)
c.1965A>T (p.Ile655=)
2g.108753477T>ACA348053055RANBP2c.1969T>A (p.Leu657Met)
c.1891T>A (p.Leu631Met)
c.1966T>A (p.Leu656Met)
2g.108753477T>CCA427909889RANBP2c.1969T>C (p.Leu657=)
c.1891T>C (p.Leu631=)
c.1966T>C (p.Leu656=)
 gnomAD v4
2g.108753477T>GCA348053058RANBP2c.1969T>G (p.Leu657Val)
c.1891T>G (p.Leu631Val)
c.1966T>G (p.Leu656Val)
2g.108753478T>ACA348053072RANBP2c.1970T>A (p.Leu657Ter)
c.1892T>A (p.Leu631Ter)
c.1967T>A (p.Leu656Ter)
2g.108753478T>CCA348053073RANBP2c.1970T>C (p.Leu657Ser)
c.1892T>C (p.Leu631Ser)
c.1967T>C (p.Leu656Ser)
 gnomAD v4
2g.108753478T>GCA348053068RANBP2c.1970T>G (p.Leu657Trp)
c.1892T>G (p.Leu631Trp)
c.1967T>G (p.Leu656Trp)
2g.108753479G>ACA427909894RANBP2c.1971G>A (p.Leu657=)
c.1893G>A (p.Leu631=)
c.1968G>A (p.Leu656=)
2g.108753479G>CCA348053075RANBP2c.1971G>C (p.Leu657Phe)
c.1893G>C (p.Leu631Phe)
c.1968G>C (p.Leu656Phe)
2g.108753479G>TCA348053077RANBP2c.1971G>T (p.Leu657Phe)
c.1893G>T (p.Leu631Phe)
c.1968G>T (p.Leu656Phe)
2g.108753480G>ACA1822500RANBP2c.1972G>A (p.Asp658Asn)
c.1894G>A (p.Asp632Asn)
c.1969G>A (p.Asp657Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.108753480G>CCA348053090RANBP2c.1972G>C (p.Asp658His)
c.1894G>C (p.Asp632His)
c.1969G>C (p.Asp657His)
2g.108753480G=CA1278286975RANBP2c.1972G= (p.Asp658=)
c.1894G= (p.Asp632=)
c.1969G= (p.Asp657=)
2g.108753480G>TCA348053091RANBP2c.1972G>T (p.Asp658Tyr)
c.1894G>T (p.Asp632Tyr)
c.1969G>T (p.Asp657Tyr)
2g.108753481A>CCA348053098RANBP2c.1973A>C (p.Asp658Ala)
c.1895A>C (p.Asp632Ala)
c.1970A>C (p.Asp657Ala)
2g.108753481A>GCA348053096RANBP2c.1973A>G (p.Asp658Gly)
c.1895A>G (p.Asp632Gly)
c.1970A>G (p.Asp657Gly)
2g.108753481A>TCA348053097RANBP2c.1973A>T (p.Asp658Val)
c.1895A>T (p.Asp632Val)
c.1970A>T (p.Asp657Val)
2g.108753482T>ACA348053100RANBP2c.1974T>A (p.Asp658Glu)
c.1896T>A (p.Asp632Glu)
c.1971T>A (p.Asp657Glu)
2g.108753482T>CCA427909897RANBP2c.1974T>C (p.Asp658=)
c.1896T>C (p.Asp632=)
c.1971T>C (p.Asp657=)
2g.108753482T>GCA348053101RANBP2c.1974T>G (p.Asp658Glu)
c.1896T>G (p.Asp632Glu)
c.1971T>G (p.Asp657Glu)
2g.108753483G>ACA348053106RANBP2c.1975G>A (p.Ala659Thr)
c.1897G>A (p.Ala633Thr)
c.1972G>A (p.Ala658Thr)
2g.108753483G>CCA348053118RANBP2c.1975G>C (p.Ala659Pro)
c.1897G>C (p.Ala633Pro)
c.1972G>C (p.Ala658Pro)
2g.108753483G=CA1278286976RANBP2c.1975G= (p.Ala659=)
c.1897G= (p.Ala633=)
c.1972G= (p.Ala658=)
2g.108753483G>TCA348053121RANBP2c.1975G>T (p.Ala659Ser)
c.1897G>T (p.Ala633Ser)
c.1972G>T (p.Ala658Ser)
 ClinVar dbSNP
2g.108753484C>ACA348053130RANBP2c.1976C>A (p.Ala659Glu)
c.1898C>A (p.Ala633Glu)
c.1973C>A (p.Ala658Glu)
2g.108753484C=CA1278286977RANBP2c.1976C= (p.Ala659=)
c.1898C= (p.Ala633=)
c.1973C= (p.Ala658=)
2g.108753484C>GCA348053135RANBP2c.1976C>G (p.Ala659Gly)
c.1898C>G (p.Ala633Gly)
c.1973C>G (p.Ala658Gly)
 dbSNP
2g.108753484C>TCA348053132RANBP2c.1976C>T (p.Ala659Val)
c.1898C>T (p.Ala633Val)
c.1973C>T (p.Ala658Val)
2g.108753485A>CCA427909900RANBP2c.1977A>C (p.Ala659=)
c.1899A>C (p.Ala633=)
c.1974A>C (p.Ala658=)
2g.108753485A>GCA427909901RANBP2c.1977A>G (p.Ala659=)
c.1899A>G (p.Ala633=)
c.1974A>G (p.Ala658=)
2g.108753485A>TCA427909902RANBP2c.1977A>T (p.Ala659=)
c.1899A>T (p.Ala633=)
c.1974A>T (p.Ala658=)
2g.108753486G>ACA348053142RANBP2c.1978G>A (p.Val660Ile)
c.1900G>A (p.Val634Ile)
c.1975G>A (p.Val659Ile)
2g.108753486G>CCA348053149RANBP2c.1978G>C (p.Val660Leu)
c.1900G>C (p.Val634Leu)
c.1975G>C (p.Val659Leu)
2g.108753486G>TCA348053147RANBP2c.1978G>T (p.Val660Leu)
c.1900G>T (p.Val634Leu)
c.1975G>T (p.Val659Leu)
2g.108753487T>ACA348053157RANBP2c.1979T>A (p.Val660Glu)
c.1901T>A (p.Val634Glu)
c.1976T>A (p.Val659Glu)
2g.108753487T>CCA348053159RANBP2c.1979T>C (p.Val660Ala)
c.1901T>C (p.Val634Ala)
c.1976T>C (p.Val659Ala)
2g.108753487T>GCA348053165RANBP2c.1979T>G (p.Val660Gly)
c.1901T>G (p.Val634Gly)
c.1976T>G (p.Val659Gly)
 gnomAD v4
2g.108753488A=CA1278286978RANBP2c.1980A= (p.Val660=)
c.1902A= (p.Val634=)
c.1977A= (p.Val659=)
2g.108753488A>CCA427909906RANBP2c.1980A>C (p.Val660=)
c.1902A>C (p.Val634=)
c.1977A>C (p.Val659=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.108753488A>GCA427909907RANBP2c.1980A>G (p.Val660=)
c.1902A>G (p.Val634=)
c.1977A>G (p.Val659=)
 dbSNP gnomAD v2 gnomAD v4
2g.108753488A>TCA427909909RANBP2c.1980A>T (p.Val660=)
c.1902A>T (p.Val634=)
c.1977A>T (p.Val659=)
2g.108753490dupCA2577064621RANBP2c.1982dup (p.Asn661LysfsTer12)
c.1904dup (p.Asn635LysfsTer12)
c.1979dup (p.Asn660LysfsTer12)
2g.108753489A=CA1278286979RANBP2c.1981A= (p.Asn661=)
c.1903A= (p.Asn635=)
c.1978A= (p.Asn660=)
2g.108753489A>CCA1822501RANBP2c.1981A>C (p.Asn661His)
c.1903A>C (p.Asn635His)
c.1978A>C (p.Asn660His)
 dbSNP ExAC gnomAD v2
2g.108753489A>GCA348053171RANBP2c.1981A>G (p.Asn661Asp)
c.1903A>G (p.Asn635Asp)
c.1978A>G (p.Asn660Asp)
2g.108753489A>TCA348053175RANBP2c.1981A>T (p.Asn661Tyr)
c.1903A>T (p.Asn635Tyr)
c.1978A>T (p.Asn660Tyr)
2g.108753490A>CCA348053176RANBP2c.1982A>C (p.Asn661Thr)
c.1904A>C (p.Asn635Thr)
c.1979A>C (p.Asn660Thr)

Number of alleles fetched