Variant #0001007044 (NC_000017.10:g.33884439A>G, NM_001129820.1:c.643T>C (SLFN14))

Chromosome 17
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.33884439A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLFN14_000008
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2072663284
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-29 15:21:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLFN14 NM_001129820.1 ?/. - c.643T>C r.(?) p.(Phe215Leu)


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