Variant #0001005895 (NC_000022.10:g.19711886C>T, NM_000407.4:c.520C>T (GP1BB))

Chromosome 22
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.19711886C>T
DNA change (hg38) -
Published as GP1BB(NM_000407.4):c.520C>T (p.(Arg174Cys))
ISCN -
DB-ID GP1BB_000051
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GP1BB NM_000407.4 -?/. - c.520C>T r.(?) p.(Arg174Cys)
SEPT5 NM_002688.5 -?/. - c.*1879C>T r.(=) p.(=)


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