Variant #0000829771 (NC_000018.9:g.29625679C>T, NM_017831.3:c.488C>T (RNF125))

Chromosome 18
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.29625679C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID RNF125_000001 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs373764886
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-12-15 17:04:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF125 NM_017831.3 ?/. - c.488C>T r.(?) p.(Ser163Leu)


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