Variant #0000548810 (NC_000012.11:g.58025071C>T, NM_133489.2:c.*5543C>T (SLC26A10))

Chromosome 12
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.58025071C>T
DNA change (hg38) g.57631288C>T
Published as B4GALNT1(NM_001478.4):c.295G>A (p.A99T)
ISCN -
DB-ID SLC26A10_000011
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B4GALNT1 NM_001478.3 ?/. - c.295G>A r.(?) p.(Ala99Thr)
SLC26A10 NM_133489.2 ?/. - c.*5543C>T r.(=) p.(=)


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