Variant #0001063890 (NC_000003.11:g.15686310C>A, NM_000060.2:c.947C>A (BTD))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.15686310C>A
DNA change (hg38) -
Published as BTD(NM_001370658.1):c.887C>A (p.(Pro296His))
ISCN -
DB-ID BTD_000175
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 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 2026-01-20 18:57:21 +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_000060.2 +?/. - c.947C>A r.(?) p.(Pro316His)
BTD NM_001370658.1 +?/. - c.887C>A r.(?) p.(Pro296His)
HACL1 NM_012260.2 +?/. - c.-43340G>T r.(?) p.(=)


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