Variant #0000288546 (NC_000001.10:g.110153101G>A, NM_005272.3:c.147C>T (GNAT2))

Chromosome 1
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.110153101G>A
DNA change (hg38) g.109610479G>A
Published as GNAT2(NM_001377295.2):c.147C>T (p.(Ile49=)), GNAT2(NM_005272.3):c.147C>T (p.I49=), GNAT2(NM_005272.5):c.147C>T (p.I49=)
ISCN -
DB-ID GNAT2_000006 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) 0.00312 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAT2 NM_005272.3 -?/. - c.147C>T r.(?) p.(Ile49=)


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