Variant #0000805125 (NC_000011.9:g.45827430_45827435dup, NM_018389.4:c.78_83dup (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.45827430_45827435dup
DNA change (hg38) -
Published as SLC35C1(NM_018389.4):c.78_83dupAGAGGC (p.E27_A28dup)
ISCN -
DB-ID SLC35C1_000021
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35C1 NM_018389.4 ?/. - c.78_83dup r.(?) p.(Glu27_Ala28dup)


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