Variant #0000802354 (NC_000006.11:g.149719102C>T, NC_000006.11(NM_015093.4):c.1765-3C>T (TAB2))

Chromosome 6
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.149719102C>T
DNA change (hg38) -
Published as TAB2(NM_015093.5):c.1765-3C>T
ISCN -
DB-ID TAB2_000043
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUMO4 NM_001002255.1 -?/. - c.-2426C>T r.(?) p.(=)
TAB2 NM_001292034.2 -?/. - c.1765-3C>T r.spl? p.?
TAB2 NM_015093.4 -?/. - c.1765-3C>T r.spl? p.?


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