Variant #0001089735 (NC_000006.11:g.117996908G>C, NM_138459.3:c.75G>C (NUS1))

Chromosome 6
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.117996908G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID NUS1_000032 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs774553541
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-09-21 10:45:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUS1 NM_138459.3 ?/. - c.75G>C r.(?) p.(Trp25Cys)


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