Variant #0000853075 (NC_000011.9:g.64514278G>A, NM_005609.2:c.2382C>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.64514278G>A
DNA change (hg38) -
Published as PYGM(NM_005609.4):c.2382C>T (p.N794=)
ISCN -
DB-ID RASGRP2_000034
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) 0.00061 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 2022-05-09 15:40:45 +02:00 (CEST)
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.2382C>T r.(?) p.(Asn794=)
RASGRP2 NM_153819.1 -?/. - c.-1603C>T r.(?) p.(=)


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