Variant #0000554006 (NC_000015.9:g.34530504T>C, NM_133647.1:c.2731A>G (SLC12A6))

Chromosome 15
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.34530504T>C
DNA change (hg38) g.34238303T>C
Published as SLC12A6(NM_001042494.1):c.2554A>G (p.(Ile852Val))
ISCN -
DB-ID SLC12A6_000052
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMC4 NM_016454.2 ?/. - c.*8515T>C r.(=) p.(=)
SLC12A6 NM_133647.1 ?/. - c.2731A>G r.(?) p.(Ile911Val)


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