Variant #0000295858 (NC_000015.9:g.34544468C>T, NM_133647.1:c.1236G>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.34544468C>T
DNA change (hg38) g.34252267C>T
Published as SLC12A6(NM_001042496.2):c.1209G>A (p.S403=)
ISCN -
DB-ID SLC12A6_000005 See all 2 reported entries
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) 0.18794 View details
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 2020-07-06 09:58:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMC4 NM_016454.2 -/. - c.*22479C>T r.(=) p.(=)
SLC12A6 NM_133647.1 -/. - c.1236G>A r.(?) p.(Ser412=)


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