Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154928675C>A | CA414913867 | F8 | c.5115G>T (p.Gln1705His) c.5010G>T (p.Gln1670His) | |
X | g.154928675C>G | CA414913869 | F8 | c.5115G>C (p.Gln1705His) c.5010G>C (p.Gln1670His) | |
X | g.154928675C>T | CA519718384 | F8 | c.5115G>A (p.Gln1705=) c.5010G>A (p.Gln1670=) | |
X | g.154928676del | CA2695237918 | F8 | c.5114del (p.Gln1705ArgfsTer26) c.5009del (p.Gln1670ArgfsTer26) | |
X | g.154928676T>A | CA414913874 | F8 | c.5114A>T (p.Gln1705Leu) c.5009A>T (p.Gln1670Leu) | |
X | g.154928676T>C | CA414913872 | F8 | c.5114A>G (p.Gln1705Arg) c.5009A>G (p.Gln1670Arg) | |
X | g.154928676T>G | CA414913871 | F8 | c.5114A>C (p.Gln1705Pro) c.5009A>C (p.Gln1670Pro) | |
X | g.154928677G>A | CA255020 | F8 | c.5113C>T (p.Gln1705Ter) c.5008C>T (p.Gln1670Ter) | ClinVar dbSNP |
X | g.154928677G>C | CA414913877 | F8 | c.5113C>G (p.Gln1705Glu) c.5008C>G (p.Gln1670Glu) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154928677G= | CA2466835765 | F8 | c.5113C= (p.Gln1705=) c.5008C= (p.Gln1670=) | |
X | g.154928677G>T | CA414913878 | F8 | c.5113C>A (p.Gln1705Lys) c.5008C>A (p.Gln1670Lys) | |
X | g.154928677_154928678dup | CA2695237921 | F8 | c.5112_5113dup (p.Gln1705LeufsTer27) c.5007_5008dup (p.Gln1670LeufsTer27) | |
X | g.154928678A= | CA2466835766 | F8 | c.5112T= (p.Asn1704=) c.5007T= (p.Asn1669=) | |
X | g.154928678A>C | CA414913880 | F8 | c.5112T>G (p.Asn1704Lys) c.5007T>G (p.Asn1669Lys) | gnomAD v4 |
X | g.154928678A>G | CA519718385 | F8 | c.5112T>C (p.Asn1704=) c.5007T>C (p.Asn1669=) | |
X | g.154928678A>T | CA414913882 | F8 | c.5112T>A (p.Asn1704Lys) c.5007T>A (p.Asn1669Lys) | |
X | g.154928679T>A | CA414913884 | F8 | c.5111A>T (p.Asn1704Ile) c.5006A>T (p.Asn1669Ile) | |
X | g.154928679T>C | CA414913886 | F8 | c.5111A>G (p.Asn1704Ser) c.5006A>G (p.Asn1669Ser) | |
X | g.154928679T>G | CA414913887 | F8 | c.5111A>C (p.Asn1704Thr) c.5006A>C (p.Asn1669Thr) | |
X | g.154928681_154928682dup | CA873340243 | F8 | c.5110_5111dup (p.Asn1704LysfsTer28) c.5005_5006dup (p.Asn1669LysfsTer28) | dbSNP |
X | g.154928682del | CA2695237923 | F8 | c.5111del (p.Asn1704IlefsTer27) c.5006del (p.Asn1669IlefsTer27) | |
X | g.154928680T>A | CA414913889 | F8 | c.5110A>T (p.Asn1704Tyr) c.5005A>T (p.Asn1669Tyr) | |
X | g.154928680T>C | CA414913891 | F8 | c.5110A>G (p.Asn1704Asp) c.5005A>G (p.Asn1669Asp) | |
X | g.154928680T>G | CA414913893 | F8 | c.5110A>C (p.Asn1704His) c.5005A>C (p.Asn1669His) | |
X | g.154928681T>A | CA414913895 | F8 | c.5109A>T (p.Glu1703Asp) c.5004A>T (p.Glu1668Asp) | |
X | g.154928681T>C | CA519718386 | F8 | c.5109A>G (p.Glu1703=) c.5004A>G (p.Glu1668=) | |
X | g.154928681T>G | CA414913897 | F8 | c.5109A>C (p.Glu1703Asp) c.5004A>C (p.Glu1668Asp) | |
X | g.154928682T>A | CA414913898 | F8 | c.5108A>T (p.Glu1703Val) c.5003A>T (p.Glu1668Val) | |
X | g.154928682T>C | CA414913899 | F8 | c.5108A>G (p.Glu1703Gly) c.5003A>G (p.Glu1668Gly) | COSMIC COSMIC |
X | g.154928682T>G | CA10568038 | F8 | c.5108A>C (p.Glu1703Ala) c.5003A>C (p.Glu1668Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
X | g.154928682T= | CA2466835767 | F8 | c.5108A= (p.Glu1703=) c.5003A= (p.Glu1668=) | |
X | g.154928683C>A | CA414913902 | F8 | c.5107G>T (p.Glu1703Ter) c.5002G>T (p.Glu1668Ter) | |
X | g.154928683C= | CA2466835768 | F8 | c.5107G= (p.Glu1703=) c.5002G= (p.Glu1668=) | |
X | g.154928683C>G | CA414913903 | F8 | c.5107G>C (p.Glu1703Gln) c.5002G>C (p.Glu1668Gln) | |
X | g.154928683C>T | CA10568039 | F8 | c.5107G>A (p.Glu1703Lys) c.5002G>A (p.Glu1668Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928684A>C | CA414913905 | F8 | c.5106T>G (p.Asp1702Glu) c.5001T>G (p.Asp1667Glu) | gnomAD v4 |
X | g.154928684A>G | CA519718387 | F8 | c.5106T>C (p.Asp1702=) c.5001T>C (p.Asp1667=) | |
X | g.154928684A>T | CA414913907 | F8 | c.5106T>A (p.Asp1702Glu) c.5001T>A (p.Asp1667Glu) | |
X | g.154928685T>A | CA414913909 | F8 | c.5105A>T (p.Asp1702Val) c.5000A>T (p.Asp1667Val) | |
X | g.154928685T>C | CA414913911 | F8 | c.5105A>G (p.Asp1702Gly) c.5000A>G (p.Asp1667Gly) | |
X | g.154928685T>G | CA414913913 | F8 | c.5105A>C (p.Asp1702Ala) c.5000A>C (p.Asp1667Ala) | |
X | g.154928686C>A | CA414913919 | F8 | c.5104G>T (p.Asp1702Tyr) c.4999G>T (p.Asp1667Tyr) | |
X | g.154928686C>G | CA414913915 | F8 | c.5104G>C (p.Asp1702His) c.4999G>C (p.Asp1667His) | |
X | g.154928686C>T | CA414913917 | F8 | c.5104G>A (p.Asp1702Asn) c.4999G>A (p.Asp1667Asn) | gnomAD v4 COSMIC COSMIC |
X | g.154928687C>A | CA414913921 | F8 | c.5103G>T (p.Glu1701Asp) c.4998G>T (p.Glu1666Asp) | |
X | g.154928687C>G | CA414913923 | F8 | c.5103G>C (p.Glu1701Asp) c.4998G>C (p.Glu1666Asp) | |
X | g.154928687C>T | CA519718388 | F8 | c.5103G>A (p.Glu1701=) c.4998G>A (p.Glu1666=) | |
X | g.154928688T>A | CA414913926 | F8 | c.5102A>T (p.Glu1701Val) c.4997A>T (p.Glu1666Val) | |
X | g.154928688T>C | CA414913928 | F8 | c.5102A>G (p.Glu1701Gly) c.4997A>G (p.Glu1666Gly) | |
X | g.154928688T>G | CA414913929 | F8 | c.5102A>C (p.Glu1701Ala) c.4997A>C (p.Glu1666Ala) |