Variant #0000726504 (NC_000017.10:g.4837744_4837748del, NM_000173.5:c.1845_1849del (GP1BA))

Chromosome 17
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.4837744_4837748del
DNA change (hg38) -
Published as GP1BA(NM_000173.7):c.1845_1849del (p.(Asn616ProfsTer29))
ISCN -
DB-ID GP1BA_000088 See all 2 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) 0.0004 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 2021-02-08 18:36:18 +01:00 (CET)
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     

Haplotype     
GP1BA NM_000173.5 ?/. - c.1845_1849del r.(?) p.(Asn616Profs*29) -
SLC25A11 NM_003562.4 ?/. - c.*3288_*3292del r.(=) p.(=) -


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