Variant #0000261365 (NC_000012.11:g.58025813G>C, NM_133489.2:c.*6285G>C (SLC26A10))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58025813G>C
DNA change (hg38) g.57632030G>C
Published as B4GALNT1(NM_001478.4):c.103C>G (p.L35V)
ISCN -
DB-ID B4GALNT1_000008
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) 0.23634 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.103C>G r.(?) p.(Leu35Val)
SLC26A10 NM_133489.2 -/. - c.*6285G>C r.(=) p.(=)


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