ClinVar

NM_001276345.2(TNNT2):c.295-17C>T

Gene:

TNNT2:troponin T2, cardiac type [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q32.1

Genomic location:

• Chr1: 201365324 (on Assembly GRCh38)
• Chr1: 201334452 (on Assembly GRCh37)

Preferred name:

NM_001276345.2(TNNT2):c.295-17C>T

HGVS:

• NC_000001.11:g.201365324G>A
• NG_007556.1:g.17354C>T
• NM_000364.4:c.295-17C>T
• NM_001001430.3:c.265-17C>T
• NM_001001431.3:c.265-17C>T
• NM_001001432.3:c.250-17C>T
• NM_001276345.2:c.295-17C>TMANE SELECT
• NM_001276346.2:c.291+286C>T
• NM_001276347.2:c.265-17C>T
• LRG_431t1:c.295-17C>T
• LRG_431:g.17354C>T
• NC_000001.10:g.201334452G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_000364.4:c.295-17C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001001430.3:c.265-17C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001001431.3:c.265-17C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001001432.3:c.250-17C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001276345.2:c.295-17C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001276346.2:c.291+286C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001276347.2:c.265-17C>T - intron variant - [Sequence Ontology: SO:0001627]