ClinVar

NM_138501.6(TECR):c.16-15G>A

Gene:

TECR:trans-2,3-enoyl-CoA reductase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.12

Genomic location:

• Chr19: 14562510 (on Assembly GRCh38)
• Chr19: 14673322 (on Assembly GRCh37)

Preferred name:

NM_138501.6(TECR):c.16-15G>A

HGVS:

• NC_000019.10:g.14562510G>A
• NG_028336.1:g.37944G>A
• NM_001321170.1:c.61-15G>A
• NM_138501.6:c.16-15G>AMANE SELECT
• NC_000019.9:g.14673322G>A
• NM_138501.4:c.16-15G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs113855270

NCBI 1000 Genomes Browser:

rs113855270

Molecular consequence:

• NM_001321170.1:c.61-15G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_138501.6:c.16-15G>A - intron variant - [Sequence Ontology: SO:0001627]

Observations:

10