Variant #0000348348 (NC_000017.10:g.72919086G>A, NM_173477.2:c.83C>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.72919086G>A
DNA change (hg38) g.74922991G>A
Published as USH1G(NM_173477.4):c.83C>T (p.P28L)
ISCN -
DB-ID USH1G_000022 See all 3 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) 0.00073 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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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.83C>T r.(?) p.(Pro28Leu) -
OTOP2 NM_178160.2 ?/. - c.-1376G>A r.(?) p.(=) -


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