Variant #0000996921 (NC_000008.10:g.125499215C>T, NM_007218.3:c.1325C>T (RNF139))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.125499215C>T
DNA change (hg38) -
Published as RNF139(NM_007218.3):c.1325C>T (p.(Thr442Met))
ISCN -
DB-ID RNF139_000002
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF139 NM_007218.3 -?/. - c.1325C>T r.(?) p.(Thr442Met)
TATDN1 NM_032026.3 -?/. - c.*1620G>A r.(=) p.(=)


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