Variant #0000890044 (NC_000011.9:g.64504329C>T, NM_153819.1:c.991G>A (RASGRP2))

Chromosome 11
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.64504329C>T
DNA change (hg38) -
Published as RASGRP2(NM_153819.1):c.991G>A (p.G331R)
ISCN -
DB-ID RASGRP2_000035
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) 0.00034 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RASGRP2 NM_001098671.2 -?/. - c.991G>A r.(?) p.(Gly331Arg)
RASGRP2 NM_153819.1 -?/. - c.991G>A r.(?) p.(Gly331Arg)


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