Variant #0000852905 (NC_000011.9:g.45827791C>T, NM_018389.4:c.439C>T (SLC35C1))

Chromosome 11
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.45827791C>T
DNA change (hg38) -
Published as SLC35C1(NM_001145265.1):c.400C>T (p.(Arg134Cys)), SLC35C1(NM_018389.4):c.439C>T (p.R147C)
ISCN -
DB-ID SLC35C1_000004 See all 3 reported entries
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35C1 NM_018389.4 ?/. - c.439C>T r.(?) p.(Arg147Cys)


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