Variant #0000281137 (NC_000023.10:g.122336603dup, GRIA3(NM_007325.4):c.268+16761dup)

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.122336603dup
DNA change (hg38) g.123202751dup
Published as GRIA3(NM_000828.4):c.268+16761dupG, GRIA3(NM_001256743.1):c.380dupG, GRIA3(NM_001256743.2):c.380dupG (p.G128Wfs*16), GRIA3(NM_001256743.2):c.384del...
ISCN -
DB-ID GRIA3_000022 See all 5 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIA3 NM_007325.4 -/. - c.268+16761dup r.(=) p.(=)