Variant #0000304889 (NC_000017.10:g.72923351G>A, NM_173477.2:c.-4183C>T (USH1G))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.72923351G>A
DNA change (hg38) g.74927256G>A
Published as OTOP2(NM_178160.2):c.484G>A (p.V162I)
ISCN -
DB-ID OTOP2_000002
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) 0.00019 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH1G NM_173477.2 ?/. - c.-4183C>T r.(?) p.(=) -
OTOP2 NM_178160.2 ?/. - c.484G>A r.(?) p.(Val162Ile) -


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