Variant #0000298231 (NC_000015.9:g.34543114_34543121del, NM_133647.1:c.1471_1478del (SLC12A6))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.34543114_34543121del
DNA change (hg38) g.34250913_34250920del
Published as SLC12A6(NM_133647.2):c.1471_1478delTTCCCTCT (p.I491Sfs*50)
ISCN -
DB-ID SLC12A6_000042
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.*21125_*21132del r.(=) p.(=)
SLC12A6 NM_133647.1 +?/. - c.1471_1478del r.(?) p.(Ile491SerfsTer50)


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