Variant #0000977023 (NC_000006.11:g.149721554A>C, NC_000006.11(NM_015093.4):c.1939+1234A>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.149721554A>C
DNA change (hg38) -
Published as SUMO4(NM_001002255.2):c.27A>C (p.(Glu9Asp))
ISCN -
DB-ID TAB2_000062
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) 0.00017 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.27A>C r.(?) p.(Glu9Asp)
TAB2 NM_001292034.2 -?/. - c.1939+1234A>C r.(=) p.(=)
TAB2 NM_015093.4 -?/. - c.1939+1234A>C r.(=) p.(=)


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