ClinVar

NM_001292034.3(TAB2):c.-89-16TTTC[4]

Gene:

TAB2:TGF-beta activated kinase 1 (MAP3K7) binding protein 2 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

6q25.1

Genomic location:

• Chr6: 149369892 - 149369893 (on Assembly GRCh38)
• Chr6: 149691028 - 149691029 (on Assembly GRCh37)

Preferred name:

NM_001292034.3(TAB2):c.-89-16TTTC[4]

HGVS:

• NC_000006.12:g.149369893TTTC[4]
• NG_021386.2:g.156970TTTC[4]
• NM_001292034.3:c.-89-16TTTC[4]MANE SELECT
• NM_001292035.3:c.7-8125TTTC[4]
• NM_001369506.1:c.-89-16TTTC[4]
• NM_015093.6:c.-89-16TTTC[4]
• NC_000006.11:g.149691029TTTC[4]

This HGVS expression did not pass validation

Links:

dbSNP: rs371930595

NCBI 1000 Genomes Browser:

rs371930595

Molecular consequence:

• NM_001292034.3:c.-89-16TTTC[4] - intron variant - [Sequence Ontology: SO:0001627]
• NM_001292035.3:c.7-8125TTTC[4] - intron variant - [Sequence Ontology: SO:0001627]
• NM_001369506.1:c.-89-16TTTC[4] - intron variant - [Sequence Ontology: SO:0001627]
• NM_015093.6:c.-89-16TTTC[4] - intron variant - [Sequence Ontology: SO:0001627]