Variant #0000549863 (NC_000013.10:g.113772772G>A, NM_000131.4:c.851G>A (F7))

Chromosome 13
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.113772772G>A
DNA change (hg38) g.113118458G>A
Published as F7(NM_000131.4):c.851G>A (p.(Arg284Gln))
ISCN -
DB-ID F7_000143
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) 0.00047 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
F7 NM_000131.4 -?/. - c.851G>A r.(?) p.(Arg284Gln)
F10 NM_000504.3 -?/. - c.-4398G>A r.(?) p.(=)


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