Variant #0000296687 (NC_000007.13:g.128415195T>G, NM_001708.2:c.366A>C (OPN1SW))

Chromosome 7
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.128415195T>G
DNA change (hg38) g.128775141T>G
Published as OPN1SW(NM_001385125.1):c.357A>C (p.G119=)
ISCN -
DB-ID OPN1SW_000004
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) 0.3015 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CALU NM_001219.4 -/. - c.*5974T>G r.(=) p.(=)
OPN1SW NM_001708.2 -/. - c.366A>C r.(?) p.(Gly122=)


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