Variant #0000562979 (NC_000017.10:g.72916226C>T, NM_173477.2:c.705G>A (USH1G))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.72916226C>T
DNA change (hg38) g.74920131C>T
Published as USH1G(NM_173477.4):c.705G>A (p.E235=), USH1G(NM_173477.5):c.705G>A (p.E235=)
ISCN -
DB-ID USH1G_000013 See all 5 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) 0.00059 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 12:25:46 +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.705G>A r.(?) p.(Glu235=) -
OTOP2 NM_178160.2 -/. - c.-4236C>T r.(?) p.(=) -


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