Variant #0000562216 (NC_000017.10:g.4836105C>T, NM_000173.5:c.206C>T (GP1BA))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4836105C>T
DNA change (hg38) g.4932810C>T
Published as GP1BA(NM_000173.5):c.206C>T (p.(Pro69Leu)), GP1BA(NM_000173.7):c.206C>T (p.P69L)
ISCN -
DB-ID GP1BA_000078 See all 3 reported entries
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) 0.00175 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
GP1BA NM_000173.5 -/. - c.206C>T - r.(?) p.(Pro69Leu)
SLC25A11 NM_003562.4 -/. - c.*4931G>A - r.(=) p.(=)


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