Variant #0000805254 (NC_000011.9:g.64514696C>T, NM_005609.2:c.2312G>A (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.64514696C>T
DNA change (hg38) -
Published as PYGM(NM_001164716.1):c.2048G>A (p.R683Q)
ISCN -
DB-ID PYGM_000123 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.2312G>A r.(?) p.(Arg771Gln)
RASGRP2 NM_153819.1 ?/. - c.-2021G>A r.(?) p.(=)


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