Variant #0000172144 (NC_000003.11:g.15686425G>A, NM_000060.2:c.1062G>A (BTD))

Chromosome 3
Allele Paternal (confirmed)
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.15686425G>A
DNA change (hg38) g.15644918G>A
Published as -
ISCN -
DB-ID BTD_000110 See all 2 reported entries
Variant remarks normal BTD activity in parent, probable in index
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency rare
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0005 View details
Owner Jasper Saris
Database submission license No license selected
Created by Jasper Saris
Date created 2011-01-17 13:52:00 +01:00 (CET)
Date last edited 2011-01-17 22:59:00 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BTD NM_000060.2 -?/. 4 c.1062G>A r.(?) p.(Thr354=)



Screenings

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