Variant #0000896041 (NC_000023.10:g.154157271C>A, NM_000132.3:c.4794G>T (F8))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.154157271C>A
DNA change (hg38) -
Published as F8(NM_000132.3):c.4794G>T (p.E1598D)
ISCN -
DB-ID F8_000732 See all 2 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) 0.00015 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F8 NM_000132.3 -?/. - c.4794G>T r.(?) p.(Glu1598Asp)
H2AFB1 NM_001017990.1 -?/. - c.*43599C>A r.(=) p.(=)
F8A1 NM_012151.3 -?/. - c.*41506C>A r.(=) p.(=)
FUNDC2 NM_023934.3 -?/. - c.-97943C>A r.(?) p.(=)


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