Variant #0000619637 (NC_000023.10:g.48762555G>C, NM_005660.1:c.631C>G (SLC35A2))

Chromosome X
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.48762555G>C
DNA change (hg38) g.48905278G>C
Published as -
ISCN -
DB-ID TIMM17B_000014
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PQBP1 NM_001032383.1 ?/. - c.*2194G>C r.(=) p.(=)
SLC35A2 NM_005660.1 ?/. - c.631C>G r.(?) p.(Leu211Val)
PQBP1 NM_005710.2 ?/. - c.*2194G>C r.(=) p.(=)
TIMM17B NM_005834.3 ?/. - c.-7278C>G r.(?) p.(=)


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