Variant #0000347160 (NC_000017.10:g.72915673G>C, NM_173477.2:c.1258C>G (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.72915673G>C
DNA change (hg38) g.74919578G>C
Published as USH1G(NM_173477.4):c.1258C>G (p.L420V)
ISCN -
DB-ID USH1G_000027 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) 0.00094 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 2019-12-04 15:24:38 +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.1258C>G r.(?) p.(Leu420Val) -
OTOP2 NM_178160.2 ?/. - c.-4789G>C r.(?) p.(=) -


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