Variant #0000326810 (NC_000019.9:g.55865861G>T, NM_001145402.1:c.*643C>A (FAM71E2))

Chromosome 19
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.55865861G>T
DNA change (hg38) g.55354493G>T
Published as COX6B2(NM_144613.4):c.29C>A (p.(Pro10His))
ISCN -
DB-ID COX6B2_000001
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) 0.00014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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     
FAM71E2 NM_001145402.1 ?/. - c.*643C>A r.(=) p.(=)
COX6B2 NM_144613.4 ?/. - c.29C>A r.(?) p.(Pro10His)


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