Variant #0000616803 (NC_000017.10:g.72916365C>T, NM_173477.2:c.566G>A (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.72916365C>T
DNA change (hg38) g.74920270C>T
Published as USH1G(NM_173477.4):c.566G>A (p.R189Q), USH1G(NM_173477.5):c.566G>A (p.R189Q)
ISCN -
DB-ID USH1G_000045 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) 0.00213 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited N/A
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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.566G>A r.(?) p.(Arg189Gln) -
OTOP2 NM_178160.2 ?/. - c.-4097C>T r.(?) p.(=) -


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