Variant #0000325134 (NC_000017.10:g.4836005A>G, NM_000173.5:c.106A>G (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.4836005A>G
DNA change (hg38) g.4932710A>G
Published as GP1BA(NM_000173.5):c.106A>G (p.(Arg36Gly))
ISCN -
DB-ID GP1BA_000031 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) 0.00151 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 2018-01-15 20:58:59 +01:00 (CET)
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.106A>G - r.(?) p.(Arg36Gly)
SLC25A11 NM_003562.4 -?/. - c.*5031T>C - r.(=) p.(=)


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