Variant #0000623210 (NC_000015.9:g.34529710T>C, NM_133647.1:c.2844A>G (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.34529710T>C
DNA change (hg38) g.34237509T>C
Published as SLC12A6(NM_001365088.1):c.2844A>G (p.Q948=), SLC12A6(NM_133647.2):c.2844A>G (p.Q948=)
ISCN -
DB-ID SLC12A6_000078 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) 2.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*7721T>C r.(=) p.(=)
SLC12A6 NM_133647.1 -?/. - c.2844A>G r.(?) p.(Gln948=)


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