Variant #0000505982 (NC_000001.10:g.235577935_235577941dup, NM_152490.3:c.*35582_*35588dup (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.235577935_235577941dup
DNA change (hg38) g.235414620_235414626dup
Published as TBCE(NM_003193.5):c.371_372insGTAAGTG (p.S124Rfs*2)
ISCN -
DB-ID TBCE_000046
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 ?/. - c.371+2_371+8dup r.spl? p.?
B3GALNT2 NM_152490.3 ?/. - c.*35582_*35588dup r.(=) p.(=)


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