Variant #0000548805 (NC_000012.11:g.58021595C>G, NM_133489.2:c.*2067C>G (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.58021595C>G
DNA change (hg38) g.57627812C>G
Published as B4GALNT1(NM_001478.4):c.1190G>C (p.R397P)
ISCN -
DB-ID SLC26A10_000007
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) 4.0E-5 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.1190G>C r.(?) p.(Arg397Pro)
SLC26A10 NM_133489.2 ?/. - c.*2067C>G r.(=) p.(=)


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