Variant #0001064656 (NC_000006.11:g.149656694G>A, NC_000006.11(NM_015093.4):c.-331-1G>A (TAB2))

Chromosome 6
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.149656694G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr6_008452
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUMO4 NM_001002255.1 ?/. - c.-64834G>A r.(?) p.(=)
TAB2 NM_001292034.2 ?/. - c.-90+17543G>A r.(=) p.(=)
TAB2 NM_015093.4 ?/. - c.-331-1G>A r.spl? p.?


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