Variant #0000904119 (NC_000018.9:g.29598907C>A, NM_017831.3:c.81C>A (RNF125))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29598907C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID RNF125_000010 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs776932441
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-11-25 10:46:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF125 NM_017831.3 +?/. - c.81C>A r.(?) p.(Asp27Glu)


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