Variant #0000995393 (NC_000006.11:g.149700588C>G, NM_015093.4:c.1537C>G (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.149700588C>G
DNA change (hg38) -
Published as TAB2(NM_015093.4):c.1537C>G (p.(His513Asp))
ISCN -
DB-ID TAB2_000066
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 2024-08-28 13:16:32 +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.-20940C>G r.(?) p.(=)
TAB2 NM_001292034.2 -?/. - c.1537C>G r.(?) p.(His513Asp)
TAB2 NM_015093.4 -?/. - c.1537C>G r.(?) p.(His513Asp)


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