Variant #0000288762 (NC_000023.10:g.122536945G>A, NM_007325.4:c.1181G>A (GRIA3))

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.122536945G>A
DNA change (hg38) g.123403094G>A
Published as GRIA3(NM_000828.4):c.1181G>A (p.R394Q), GRIA3(NM_007325.4):c.1181G>A (p.W394*)
ISCN -
DB-ID GRIA3_000049 See all 2 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) 0.00149 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIA3 NM_007325.4 -/. - c.1181G>A r.(?) p.(Arg394Gln)


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