Variant #0000267961 (NC_000023.10:g.154158201T>G, NM_000132.3:c.3864A>C (F8))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.154158201T>G
DNA change (hg38) g.154929926T>G
Published as F8(NM_000132.3):c.3864A>C (p.S1288=), F8(NM_000132.4):c.3864A>C (p.S1288=)
ISCN -
DB-ID F8_000062 See all 15 reported entries
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) 0.14699 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.3864A>C r.(?) p.(Ser1288=)
H2AFB1 NM_001017990.1 -/. - c.*44529T>G r.(=) p.(=)
F8A1 NM_012151.3 -/. - c.*42436T>G r.(=) p.(=)
FUNDC2 NM_023934.3 -/. - c.-97013T>G r.(?) p.(=)


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