Variant #0000272231 (NC_000016.9:g.19566892C>T, NM_020314.5:c.108C>T (C16orf62))

Chromosome 16
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.19566892C>T
DNA change (hg38) g.19555570C>T
Published as VPS35L(NM_020314.6):c.-160C>T
ISCN -
DB-ID C16orf62_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-09 14:00:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCP110 NM_014711.4 -?/. - c.*4299C>T r.(=) p.(=)
C16orf62 NM_020314.5 -?/. - c.108C>T r.(?) p.(Cys36=)


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