Variant #0000527429 (NC_000006.11:g.149721690G>A, NC_000006.11(NM_015093.4):c.1939+1370G>A (TAB2))

Chromosome 6
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.149721690G>A
DNA change (hg38) g.149400554G>A
Published as SUMO4(NM_001002255.2):c.163G>A (p.V55M), TAB2(NM_015093.5):c.1939+1370G>A
ISCN -
DB-ID SUMO4_000002 See all 4 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) 0.55275 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +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.163G>A r.(?) p.(Val55Met)
TAB2 NM_001292034.2 -/. - c.1939+1370G>A r.(=) p.(=)
TAB2 NM_015093.4 -/. - c.1939+1370G>A r.(=) p.(=)


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