Variant #0000255387 (NC_000003.11:g.15686731A>C, NM_000060.2:c.1368A>C (BTD))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.15686731A>C
DNA change (hg38) g.15645224A>C
Published as BTD(NM_000060.4):c.1368A>C (p.Q456H), BTD(NM_001281723.3):c.1308A>C (p.Q436H), BTD(NM_001281723.4):c.1308A>C (p.Q436H), BTD(NM_001370658.1):c.1308A...
ISCN -
DB-ID BTD_000027 See all 30 reported entries
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) 0.00039 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BTD NM_000060.2 +/. - c.1368A>C r.(?) p.(Gln456His)
HACL1 NM_012260.2 +/. - c.-43761T>G r.(?) p.(=)


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