Variant #0000799176 (NC_000001.10:g.235599877T>C, NM_152490.3:c.*13644A>G (B3GALNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.235599877T>C
DNA change (hg38) -
Published as TBCE(NM_001079515.1):c.917T>C (p.(Phe306Ser)), TBCE(NM_001287801.2):c.1070T>C (p.F357S)
ISCN -
DB-ID TBCE_000021 See all 2 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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +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     
TBCE NM_003193.3 ?/. - c.917T>C r.(?) p.(Phe306Ser)
B3GALNT2 NM_152490.3 ?/. - c.*13644A>G r.(=) p.(=)


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