Variant #0000613532 (NC_000011.9:g.64510322T>C, NM_005609.2:c.*3809A>G (PYGM))

Chromosome 11
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.64510322T>C
DNA change (hg38) g.64742850T>C
Published as RASGRP2(NM_001098670.1):c.17A>G (p.(Asp6Gly))
ISCN -
DB-ID RASGRP2_000015
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) 0.00028 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 2019-12-04 15:24:38 +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     
PYGM NM_005609.2 ?/. - c.*3809A>G r.(=) p.(=)
RASGRP2 NM_153819.1 ?/. - c.17A>G r.(?) p.(Asp6Gly)


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