Variant #0000550184 (NC_000013.10:g.31843415G>A, NC_000013.10(NM_194318.3):c.660+1G>A (B3GLCT))

Chromosome 13
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.31843415G>A
DNA change (hg38) g.31269278G>A
Published as B3GALTL(NM_194318.3):c.660+1G>A (p.?), B3GLCT(NM_194318.3):c.660+1G>A, B3GLCT(NM_194318.4):c.660+1G>A
ISCN -
DB-ID B3GLCT_000002 See all 32 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) 0.00071 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GLCT NM_194318.3 +/. - c.660+1G>A r.spl? p.?


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