Variant #0000865486 (NC_000017.10:g.72919053G>A, NM_173477.2:c.116C>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.72919053G>A
DNA change (hg38) -
Published as USH1G(NM_173477.4):c.116C>T (p.A39V)
ISCN -
DB-ID OTOP2_000012
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH1G NM_173477.2 ?/. - c.116C>T r.(?) p.(Ala39Val) -
OTOP2 NM_178160.2 ?/. - c.-1409G>A r.(?) p.(=) -


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