Variant #0001039638 (NC_000013.10:g.31821177C>T, NM_194318.3:c.288C>T (B3GLCT))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31821177C>T
DNA change (hg38) -
Published as B3GLCT(NM_194318.3):c.288C>T (p.L96=), B3GLCT(NM_194318.4):c.288C>T (p.(Leu96=))
ISCN -
DB-ID B3GLCT_000028 See all 4 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) 0.00055 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 2025-05-05 21:14:00 +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     
B3GLCT NM_194318.3 -?/. - c.288C>T r.(?) p.(Leu96=)


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