ClinVar

NM_007327.4(GRIN1):c.672-215C>T

Gene:

GRIN1:glutamate ionotropic receptor NMDA type subunit 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q34.3

Genomic location:

• Chr9: 137156454 (on Assembly GRCh38)
• Chr9: 140050906 (on Assembly GRCh37)

Preferred name:

NM_007327.4(GRIN1):c.672-215C>T

HGVS:

• NC_000009.12:g.137156454C>T
• NG_011507.1:g.22298C>T
• NM_000832.7:c.672-215C>T
• NM_001185090.2:c.735-215C>T
• NM_001185091.2:c.735-215C>T
• NM_007327.4:c.672-215C>TMANE SELECT
• NM_021569.4:c.672-215C>T
• NC_000009.11:g.140050906C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs144887370

NCBI 1000 Genomes Browser:

rs144887370

Molecular consequence:

• NM_000832.7:c.672-215C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001185090.2:c.735-215C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001185091.2:c.735-215C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_007327.4:c.672-215C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_021569.4:c.672-215C>T - intron variant - [Sequence Ontology: SO:0001627]