Variant #0000853474 (NC_000012.11:g.58021913G>A, NM_133489.2:c.*2385G>A (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.58021913G>A
DNA change (hg38) -
Published as B4GALNT1(NM_001478.4):c.1135C>T (p.L379=)
ISCN -
DB-ID B4GALNT1_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) 0.00136 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B4GALNT1 NM_001478.3 -?/. - c.1135C>T r.(?) p.(Leu379=)
SLC26A10 NM_133489.2 -?/. - c.*2385G>A r.(=) p.(=)


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