Variant #0000271339 (NC_000023.10:g.154132580G>A, NM_000132.3:c.5806C>T (F8))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.154132580G>A
DNA change (hg38) g.154904305G>A
Published as F8(NM_000132.3):c.5806C>T (p.R1936C)
ISCN -
DB-ID F8_001987
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) 3.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F8 NM_000132.3 +?/. - c.5806C>T r.(?) p.(Arg1936Cys)
H2AFB1 NM_001017990.1 +?/. - c.*18908G>A r.(=) p.(=)
F8A1 NM_012151.3 +?/. - c.*16815G>A r.(=) p.(=)
FUNDC2 NM_023934.3 +?/. - c.-122634G>A r.(?) p.(=)


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