Variant #0001035516 (NC_000006.11:g.149678566A>C, NC_000006.11(NM_015093.4):c.-89-12479A>C (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.149678566A>C
DNA change (hg38) -
Published as TAB2(NM_001292034.3):c.-89-12479A>C
ISCN -
DB-ID TAB2_000070
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
SUMO4 NM_001002255.1 -?/. - c.-42962A>C r.(?) p.(=)
TAB2 NM_001292034.2 -?/. - c.-89-12479A>C r.(=) p.(=)
TAB2 NM_015093.4 -?/. - c.-89-12479A>C r.(=) p.(=)


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