Variant #0000575012 (NC_000023.10:g.154132688T>A, NM_000132.3:c.5698A>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.154132688T>A
DNA change (hg38) g.154904413T>A
Published as F8(NM_000132.3):c.5698A>T (p.T1900S)
ISCN -
DB-ID F8_002044
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.5698A>T r.(?) p.(Thr1900Ser)
H2AFB1 NM_001017990.1 -?/. - c.*19016T>A r.(=) p.(=)
F8A1 NM_012151.3 -?/. - c.*16923T>A r.(=) p.(=)
FUNDC2 NM_023934.3 -?/. - c.-122526T>A r.(?) p.(=)


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