Variant #0000562983 (NC_000017.10:g.72919052A>C, NM_173477.2:c.117T>G (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.72919052A>C
DNA change (hg38) g.74922957A>C
Published as USH1G(NM_173477.5):c.117T>G (p.A39=)
ISCN -
DB-ID OTOP2_000007
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_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 12:29:05 +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.117T>G r.(?) p.(Ala39=) -
OTOP2 NM_178160.2 -/. - c.-1410A>C r.(?) p.(=) -


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