Variant #0000505978 (NC_000001.10:g.235543528_235543529del, NM_152490.3:c.*70043_*70044del (B3GALNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.235543528_235543529del
DNA change (hg38) g.235380213_235380214del
Published as TBCE(NM_001079515.2):c.100+64_100+65delGT, TBCE(NM_001287801.2):c.100+64_100+65delGT
ISCN -
DB-ID TBCE_000043 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 -/. - c.100+64_100+65del r.(=) p.(=)
B3GALNT2 NM_152490.3 -/. - c.*70043_*70044del r.(=) p.(=)


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