Variant #0000914892 (NC_000017.10:g.4837783C>T, NM_000173.5:c.1884C>T (GP1BA))

Chromosome 17
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.4837783C>T
DNA change (hg38) -
Published as GP1BA(NM_000173.7):c.1884C>T (p.P628=)
ISCN -
DB-ID GP1BA_000095
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     

Haplotype     
GP1BA NM_000173.5 -?/. - c.1884C>T r.(?) p.(Pro628=) -
SLC25A11 NM_003562.4 -?/. - c.*3253G>A r.(=) p.(=) -


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