Variant #0000288524 (NC_000023.10:g.102968544C>T, NM_001024452.2:c.987G>A (GLRA4))

Chromosome X
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.102968544C>T
DNA change (hg38) g.103713616C>T
Published as GLRA4(NM_001024452.2):c.987G>A (p.V329=), TMEM31(NM_182541.2):c.125C>T (p.T42I)
ISCN -
DB-ID GLRA4_000003
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) 1.0E-5 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 2020-07-20 18:43:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLRA4 NM_001024452.2 -/. - c.987G>A r.(?) p.(Val329=)
TMEM31 NM_182541.2 -/. - c.125C>T r.(?) p.(Thr42Ile)


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