Variant #0000575006 (NC_000023.10:g.154124460_154124461insGT, NM_000132.3:c.6320_6321insAC (F8))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.154124460_154124461insGT
DNA change (hg38) g.154896185_154896186insGT
Published as F8(NM_000132.3):c.6320_6321insAC (p.A2108Lfs*36)
ISCN -
DB-ID F8_002040
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-22 09:56:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F8 NM_000132.3 +/. - c.6320_6321insAC r.(?) p.(Ala2108LeufsTer36)
H2AFB1 NM_001017990.1 +/. - c.*10788_*10789insGT r.(=) p.(=)
F8A1 NM_012151.3 +/. - c.*8695_*8696insGT r.(=) p.(=)
FUNDC2 NM_023934.3 +/. - c.-130754_-130753insGT r.(?) p.(=)


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