Variant #0000322969 (NC_000012.11:g.58017626G>A, NM_133489.2:c.1061G>A (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.58017626G>A
DNA change (hg38) g.57623843G>A
Published as SLC26A10(NM_133489.2):c.1061G>A (p.(Gly354Asp))
ISCN -
DB-ID SLC26A10_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B4GALNT1 NM_001478.3 ?/. - c.*2901C>T r.(=) p.(=)
SLC26A10 NM_133489.2 ?/. - c.1061G>A r.(?) p.(Gly354Asp)


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