Variant #0000288522 (NC_000023.10:g.102974035C>T, NM_001024452.2:c.883G>A (GLRA4))

Chromosome X
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.102974035C>T
DNA change (hg38) g.103719107C>T
Published as GLRA4(NM_001172285.1):c.883G>A (p.V295M)
ISCN -
DB-ID GLRA4_000006
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) 0.00031 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLRA4 NM_001024452.2 -?/. - c.883G>A r.(?) p.(Val295Met)
TMEM31 NM_182541.2 -?/. - c.*5109C>T r.(=) p.(=)


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