Variant #0000804245 (NC_000010.10:g.101474456G>A, NM_078470.4:c.1121C>T (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.101474456G>A
DNA change (hg38) -
Published as COX15(NM_078470.6):c.1121C>T (p.T374M)
ISCN -
DB-ID COX15_000022
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) 3.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX15 NM_004376.5 ?/. - c.1102-1220C>T r.(=) p.(=)
CUTC NM_015960.2 ?/. - c.-17650G>A r.(?) p.(=)
ENTPD7 NM_020354.3 ?/. - c.*10016G>A r.(=) p.(=)
COX15 NM_078470.4 ?/. - c.1121C>T r.(?) p.(Thr374Met)


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