Variant #0000722628 (NC_000010.10:g.101489421C>T, COX15(NM_078470.4):c.161G>A)

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.101489421C>T
DNA change (hg38) -
Published as COX15(NM_078470.4):c.161G>A (p.G54E)
ISCN -
DB-ID COX15_000014
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX15 NM_004376.5 ?/. - c.161G>A r.(?) p.(Gly54Glu)
CUTC NM_015960.2 ?/. - c.-2685C>T r.(?) p.(=)
ENTPD7 NM_020354.3 ?/. - c.*24981C>T r.(=) p.(=)
COX15 NM_078470.4 ?/. - c.161G>A r.(?) p.(Gly54Glu)