Variant #0000994896 (NC_000005.9:g.176048219G>T, NM_052899.2:c.-11263C>A (GPRIN1))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.176048219G>T
DNA change (hg38) -
Published as SNCB(NM_003085.3):c.368C>A (p.(Pro123His))
ISCN -
DB-ID GPRIN1_000004
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) 0.00018 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNCB NM_001001502.1 ?/. - c.368C>A r.(?) p.(Pro123His)
GPRIN1 NM_052899.2 ?/. - c.-11263C>A r.(?) p.(=)


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