Transcript #00000041 (NM_000132.3, F8 gene)

Transcript name transcript variant 1
Gene name F8 (coagulation factor VIII)
Chromosome X
Transcript - NCBI ID NM_000132.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000123.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

45 entries on 1 page. Showing entries 1 - 45.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. 3 c.274G>A - r.(?) p.(Gly92Ser) - -
+/. 3 c.274G>C - r.(?) p.(Gly92Arg) - -
+/. 4 c.524A>C - r.(?) p.(Tyr175Ser) - -
+/. 4 c.554_555del - r.(?) p.(Lys185Argfs*14) - -
+/. 6i c.787+1G>A - r.spl? p.? - -
+/. 6i c.787+1G>T - r.spl? p.? - -
+/. 7 c.1007A>C - r.(?) p.(His336Pro) - -
+/. 8 c.1016T>G - r.(?) p.(Met339Arg) - -
+/. 8 c.1171C>T - r.(?) p.(Arg391Cys) - ClinVar
+/. 9 c.1354G>T - r.(?) p.(Asp452Tyr) - -
+/. 9 c.1443G>A - r.(=) p.(=) - -
+/. 11 c.1696C>T - r.(?) p.(Leu566Phe) - -
+/. 12 c.1812G>C - r.(?) p.(Trp604Cys) - ClinVar
+/. 14 c.2159G>T - r.(?) p.(Gly720Val) - -
-?/. 14 c.2383A>G - r.(?) p.(Arg795Gly) - ClinVar
+/. 14 c.2696delG - r.(?) p.(Ser899Ilefs*6) - -
+/. 14 c.3078A>C - r.(=) p.(=) - -
+/. 14 c.3175delA - r.(?) p.(Val1061*) - -
+/. 14 c.3175delA - r.(?) p.(Val1061*) - -
+/. 14 c.3180A>T - r.(?) p.(Lys1060Asn) - -
+/. 14 c.3325C>T - r.(?) p.(Gln1109*) - -
+/. 14 c.3611dupA - r.(?) p.(Asn1204Lysfs*2) - -
+/. 14 c.3625C>T - r.(?) p.(Gln1209*) - -
+/. 14 c.3629dupA - r.(?) p.(Ile1213Asnfs*28) - -
+/. 14 c.3629dupA - r.(?) p.(Ile1213Asnfs*28) - -
+/. 14 c.3637delA - r.(?) p.(Ile1213Phefs*5) - ClinVar
+/. 14 c.3762delT - r.(?) p.(Asn1254Lysfs*2) - -
-/. 14 c.3864A>C - r.(=) p.(=) - ClinVar
+/. 14 c.4156C>T - r.(?) p.(Gln1386*) - -
+/. 14 c.4820dupA - r.(?) p.(Thr1609Asnfs*4) - -
+/. 14 c.4946_4947del - r.(?) p.(Gly1649Glufs*3) - -
+/. 16i c.5586+2T>G - r.spl? p.? - -
+/. 17 c.5609T>C - r.(?) p.(Leu1870Pro) - -
+/. 17 c.5689_5690delCT - r.(?) p.(Leu1897Valfs*6) - -
+/. 18 c.5879G>A - r.(?) p.(Arg1960Gln) - ClinVar
+/. 18 c.5941G>A - r.(?) p.(Val1981Met) - -
+/. 18i c.5998+1G>A - r.spl? p.? - -
+/. 19 c.6085A>T - r.(?) p.(Met2029Leu) - -
+/. 21 c.6272A>C - r.(?) p.(Lys2091Thr) - -
+/. 22 c.6317A>C - r.(?) p.(Gln2106Pro) - -
+/. 23 c.6355delC - r.(?) p.(Gln2119Serfs*24) - -
+/. 22i c.6429+2T>A - r.spl? p.? - -
+/. 24 c.6682C>T - r.(?) p.(Arg2228*) - ClinVar
+/. 25 c.6857A>T - r.(?) p.(Asp2286Val) - -
+/. 26 c.6986C>G - r.(?) p.(Pro2329Arg) - -
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