Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154928667_154928668delinsCG | CA2466835761 | F8 | c.5122_5123delinsCG (p.Arg1708=) c.5017_5018delinsCG (p.Arg1673=) | |
X | g.154928668G>A | CA120919 | F8 | c.5122C>T (p.Arg1708Cys) c.5017C>T (p.Arg1673Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.154928668G>C | CA414913845 | F8 | c.5122C>G (p.Arg1708Gly) c.5017C>G (p.Arg1673Gly) | |
X | g.154928668G= | CA2466835762 | F8 | c.5122C= (p.Arg1708=) c.5017C= (p.Arg1673=) | |
X | g.154928668G>T | CA414913844 | F8 | c.5122C>A (p.Arg1708Ser) c.5017C>A (p.Arg1673Ser) | dbSNP |
X | g.154928672del | CA873340216 | F8 | c.5122del (p.Arg1708AlafsTer23) c.5017del (p.Arg1673AlafsTer23) | dbSNP |
X | g.154928669G>A | CA519718380 | F8 | c.5121C>T (p.Pro1707=) c.5016C>T (p.Pro1672=) | |
X | g.154928669G>C | CA519718381 | F8 | c.5121C>G (p.Pro1707=) c.5016C>G (p.Pro1672=) | |
X | g.154928669G>T | CA519718382 | F8 | c.5121C>A (p.Pro1707=) c.5016C>A (p.Pro1672=) | gnomAD v4 |
X | g.154928670G>A | CA10568036 | F8 | c.5120C>T (p.Pro1707Leu) c.5015C>T (p.Pro1672Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928670G>C | CA414913848 | F8 | c.5120C>G (p.Pro1707Arg) c.5015C>G (p.Pro1672Arg) | |
X | g.154928670G= | CA2466835763 | F8 | c.5120C= (p.Pro1707=) c.5015C= (p.Pro1672=) | |
X | g.154928670G>T | CA414913847 | F8 | c.5120C>A (p.Pro1707His) c.5015C>A (p.Pro1672His) | |
X | g.154928671G>A | CA414913850 | F8 | c.5119C>T (p.Pro1707Ser) c.5014C>T (p.Pro1672Ser) | |
X | g.154928671G>C | CA414913853 | F8 | c.5119C>G (p.Pro1707Ala) c.5014C>G (p.Pro1672Ala) | |
X | g.154928671G>T | CA414913851 | F8 | c.5119C>A (p.Pro1707Thr) c.5014C>A (p.Pro1672Thr) | |
X | g.154928672G>A | CA519718383 | F8 | c.5118C>T (p.Ser1706=) c.5013C>T (p.Ser1671=) | gnomAD v4 |
X | g.154928672G>C | CA414913854 | F8 | c.5118C>G (p.Ser1706Arg) c.5013C>G (p.Ser1671Arg) | |
X | g.154928672G>T | CA414913856 | F8 | c.5118C>A (p.Ser1706Arg) c.5013C>A (p.Ser1671Arg) | gnomAD v4 |
X | g.154928673C>A | CA10568037 | F8 | c.5117G>T (p.Ser1706Ile) c.5012G>T (p.Ser1671Ile) | dbSNP ExAC |
X | g.154928673C= | CA2466835764 | F8 | c.5117G= (p.Ser1706=) c.5012G= (p.Ser1671=) | |
X | g.154928673C>G | CA414913858 | F8 | c.5117G>C (p.Ser1706Thr) c.5012G>C (p.Ser1671Thr) | |
X | g.154928673C>T | CA414913860 | F8 | c.5117G>A (p.Ser1706Asn) c.5012G>A (p.Ser1671Asn) | gnomAD v4 |
X | g.154928674T>A | CA414913862 | F8 | c.5116A>T (p.Ser1706Cys) c.5011A>T (p.Ser1671Cys) | |
X | g.154928674T>C | CA414913864 | F8 | c.5116A>G (p.Ser1706Gly) c.5011A>G (p.Ser1671Gly) | |
X | g.154928674T>G | CA414913865 | F8 | c.5116A>C (p.Ser1706Arg) c.5011A>C (p.Ser1671Arg) | |
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) |