Variant #0000978854 (NC_000010.10:g.101473744_101473745del, NM_078470.4:c.*614_*615del (COX15))

Chromosome 10
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.101473744_101473745del
DNA change (hg38) -
Published as COX15(NM_001372024.1):c.1102-9_1102-8del
ISCN -
DB-ID COX15_000024
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX15 NM_004376.5 -?/. - c.1102-494_1102-493del r.(=) p.(=)
CUTC NM_015960.2 -?/. - c.-18362_-18361del r.(?) p.(=)
ENTPD7 NM_020354.3 -?/. - c.*9304_*9305del r.(=) p.(=)
COX15 NM_078470.4 -?/. - c.*614_*615del r.(=) p.(=)


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