Variant #0000976675 (NC_000005.9:g.151266335C>T, NM_001146040.1:c.199G>A (GLRA1))

Chromosome 5
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.151266335C>T
DNA change (hg38) -
Published as GLRA1(NM_000171.4):c.199G>A (p.(Val67Met)), GLRA1(NM_001146040.2):c.199G>A (p.V67M)
ISCN -
DB-ID GLRA1_000030 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) 0.00016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
GLRA1 NM_001146040.1 ?/. - c.199G>A r.(?) p.(Val67Met)


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