Variant #0000554035 (NC_000015.9:g.34634020C>T, NM_133647.1:c.-5139G>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.34634020C>T
DNA change (hg38) g.34341819C>T
Published as NOP10(NM_018648.3):c.*149G>A
ISCN -
DB-ID NOP10_000010 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*112031C>T r.(=) p.(=)
NOP10 NM_018648.3 -/. - c.*149G>A r.(=) p.(=)
SLC12A6 NM_133647.1 -/. - c.-5139G>A r.(?) p.(=)
C15orf55 NM_175741.1 -/. - c.-4201C>T r.(?) p.(=)


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