Variant #0001021203 (NC_000003.11:g.15686568A>G, NM_001370658.1:c.1145A>G (BTD))

Chromosome 3
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.15686568A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID BTD_000169
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs201023772
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00017 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-01-21 10:36:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BTD NM_001370658.1 ?/. - c.1145A>G r.(?) p.(Asn382Ser)


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