Variant #0000295856 (NC_000015.9:g.34629024C>T, NM_133647.1:c.-143G>A (SLC12A6))

Chromosome 15
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.34629024C>T
DNA change (hg38) g.34336823C>T
Published as SLC12A6(NM_133647.2):c.-143G>A
ISCN -
DB-ID SLC12A6_000033
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMC4 NM_016454.2 -/. - c.*107035C>T r.(=) p.(=)
NOP10 NM_018648.3 -/. - c.*5145G>A r.(=) p.(=)
SLC12A6 NM_133647.1 -/. - c.-143G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.