ClinVar

NM_001193313.2(SUGCT):c.227-66A>T

Gene:

SUGCT:succinyl-CoA:glutarate-CoA transferase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7p14.1

Genomic location:

• Chr7: 40188429 (on Assembly GRCh38)
• Chr7: 40228028 (on Assembly GRCh37)

Preferred name:

NM_001193313.2(SUGCT):c.227-66A>T

HGVS:

• NC_000007.14:g.40188429A>T
• NG_023422.2:g.58454A>T
• NM_001193311.2:c.227-66A>T
• NM_001193312.2:c.227-66A>T
• NM_001193313.2:c.227-66A>TMANE SELECT
• NM_024728.3:c.227-66A>T
• NC_000007.13:g.40228028A>T

This HGVS expression did not pass validation

Links:

dbSNP: rs644966

NCBI 1000 Genomes Browser:

rs644966

Molecular consequence:

• NM_001193311.2:c.227-66A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001193312.2:c.227-66A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001193313.2:c.227-66A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_024728.3:c.227-66A>T - intron variant - [Sequence Ontology: SO:0001627]