Variant #0000548808 (NC_000012.11:g.58023868C>T, NM_133489.2:c.*4340C>T (SLC26A10))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58023868C>T
DNA change (hg38) g.57630085C>T
Published as B4GALNT1(NM_001276469.1):c.779G>A (p.G260E)
ISCN -
DB-ID SLC26A10_000009
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) 0.00015 View details
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.712+67G>A r.(=) p.(=)
SLC26A10 NM_133489.2 -?/. - c.*4340C>T r.(=) p.(=)


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