Variant #0000890047 (NC_000011.9:g.64509596G>A, NM_005609.2:c.*4535C>T (PYGM))

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.64509596G>A
DNA change (hg38) -
Published as RASGRP2(NM_153819.1):c.74-12C>T
ISCN -
DB-ID RASGRP2_000036
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) 1.0E-5 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PYGM NM_005609.2 -?/. - c.*4535C>T r.(=) p.(=)
RASGRP2 NM_153819.1 -?/. - c.74-12C>T r.(=) p.(=)


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