Variant #0000929277 (NC_000007.13:g.128415071C>T, NM_001708.2:c.490G>A (OPN1SW))

Chromosome 7
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.128415071C>T
DNA change (hg38) -
Published as OPN1SW(NM_001385125.1):c.481G>A (p.V161I), OPN1SW(NM_001708.2):c.490G>A (p.V164I)
ISCN -
DB-ID CALU_000011 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) 0.00218 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CALU NM_001219.4 -?/. - c.*5850C>T r.(=) p.(=)
OPN1SW NM_001708.2 -?/. - c.490G>A r.(?) p.(Val164Ile)


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