Variant #0000256668 (NC_000015.9:g.34544437A>G, NM_133647.1:c.1267T>C (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.34544437A>G
DNA change (hg38) g.34252236A>G
Published as SLC12A6(NM_001042496.1):c.1240T>C (p.Y414H)
ISCN -
DB-ID SLC12A6_000043
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*22448A>G r.(=) p.(=)
SLC12A6 NM_133647.1 ?/. - c.1267T>C r.(?) p.(Tyr423His)


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