Variant #0000616933 (NC_000017.10:g.80404516T>C, NM_001033046.3:c.184A>G (C17orf62))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.80404516T>C
DNA change (hg38) g.82446640T>C
Published as C17orf62(NM_001193653.1):c.184A>G (p.N62D)
ISCN -
DB-ID C17orf62_000004
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) 0.00069 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 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     
C17orf62 NM_001033046.3 ?/. - c.184A>G r.(?) p.(Asn62Asp)
HEXDC NM_173620.2 ?/. - c.*4048T>C r.(=) p.(=)
OGFOD3 NM_175902.4 ?/. - c.-28155A>G r.(?) p.(=)


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