Variant #0000554015 (NC_000015.9:g.34543180C>G, NM_133647.1:c.1412G>C (SLC12A6))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34543180C>G
DNA change (hg38) g.34250979C>G
Published as SLC12A6(NM_001042496.1):c.1385G>C (p.S462T), SLC12A6(NM_001042496.2):c.1385G>C (p.S462T), SLC12A6(NM_133647.2):c.1412G>C (p.S471T)
ISCN -
DB-ID SLC12A6_000058 See all 3 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) 0.00576 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +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.*21191C>G r.(=) p.(=)
SLC12A6 NM_133647.1 -?/. - c.1412G>C r.(?) p.(Ser471Thr)


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