Variant #0000288763 (NC_000023.10:g.122319733T>C, GRIA3(NM_007325.4):c.159T>C)

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.122319733T>C
DNA change (hg38) g.123185881T>C
Published as GRIA3(NM_001256743.1):c.158T>C (p.F53S), GRIA3(NM_001256743.2):c.158T>C (p.F53S)
ISCN -
DB-ID GRIA3_000038 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) 0.00088 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIA3 NM_007325.4 -?/. - c.159T>C r.(?) p.(Phe53=)