Variant #0000531391 (NC_000007.13:g.151483595G>A, NM_016203.3:c.147C>T (PRKAG2))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.151483595G>A
DNA change (hg38) g.151786509G>A
Published as PRKAG2(NM_016203.3):c.147C>T (p.D49=), PRKAG2(NM_016203.4):c.147C>T (p.D49=)
ISCN -
DB-ID PRKAG2_000059 See all 3 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) 5.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKAG2 NM_016203.3 -/. - c.147C>T r.(?) p.(Asp49=)


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