Variant #0000615235 (NC_000015.9:g.34635241C>G, NM_133647.1:c.-6360G>C (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.34635241C>G
DNA change (hg38) g.34343040C>G
Published as NOP10(NM_018648.3):c.34G>C (p.(Asp12His))
ISCN -
DB-ID NOP10_000002 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) 0.01001 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +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.*113252C>G r.(=) p.(=)
NOP10 NM_018648.3 -?/. - c.34G>C r.(?) p.(Asp12His)
SLC12A6 NM_133647.1 -?/. - c.-6360G>C r.(?) p.(=)
C15orf55 NM_175741.1 -?/. - c.-2980C>G r.(?) p.(=)


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