Variant #0000911847 (NC_000003.11:g.15686296T>G, NM_000060.2:c.933T>G (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.15686296T>G
DNA change (hg38) -
Published as BTD(NM_001370658.1):c.873T>G (p.S291R)
ISCN -
DB-ID BTD_000158
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BTD NM_000060.2 +?/. - c.933T>G r.(?) p.(Ser311Arg)
BTD NM_001370658.1 +?/. - c.873T>G r.(?) p.(Ser291Arg)
HACL1 NM_012260.2 +?/. - c.-43326A>C r.(?) p.(=)


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