Variant #0000804246 (NC_000010.10:g.101478185G>C, NM_078470.4:c.905C>G (COX15))

Chromosome 10
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.101478185G>C
DNA change (hg38) -
Published as COX15(NM_078470.4):c.905C>G (p.P302R)
ISCN -
DB-ID COX15_000023
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX15 NM_004376.5 ?/. - c.905C>G r.(?) p.(Pro302Arg)
CUTC NM_015960.2 ?/. - c.-13921G>C r.(?) p.(=)
ENTPD7 NM_020354.3 ?/. - c.*13745G>C r.(=) p.(=)
COX15 NM_078470.4 ?/. - c.905C>G r.(?) p.(Pro302Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.