Variant #0000975644 (NC_000003.11:g.15686958C>T, NM_000060.2:c.1595C>T (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.15686958C>T
DNA change (hg38) -
Published as BTD(NM_000060.4):c.1595C>T (p.T532M), BTD(NM_001281723.3):c.1535C>T (p.T512M)
ISCN -
DB-ID BTD_000039 See all 14 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) 7.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.1595C>T r.(?) p.(Thr532Met)
HACL1 NM_012260.2 +?/. - c.-43988G>A r.(?) p.(=)


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