Variant #0000691778 (NC_000015.9:g.34634318G>A, NM_133647.1:c.-5437C>T (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.34634318G>A
DNA change (hg38) -
Published as NOP10(NM_018648.3):c.55-9C>T
ISCN -
DB-ID C15orf55_000003 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) 0.00022 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMC4 NM_016454.2 -?/. - c.*112329G>A r.(=) p.(=)
NOP10 NM_018648.3 -?/. - c.55-9C>T r.(=) p.(=)
SLC12A6 NM_133647.1 -?/. - c.-5437C>T r.(?) p.(=)
C15orf55 NM_175741.1 -?/. - c.-3903G>A r.(?) p.(=)


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