ClinVar

NM_012210.4(TRIM32):c.27G>A (p.Leu9=)

Genes:

ASTN2:astrotactin 2 [Gene - OMIM - HGNC]
TRIM32:tripartite motif containing 32 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q33.1

Genomic location:

• Chr9: 116697769 (on Assembly GRCh38)
• Chr9: 119460048 (on Assembly GRCh37)

Preferred name:

NM_012210.4(TRIM32):c.27G>A (p.Leu9=)

HGVS:

• NC_000009.12:g.116697769G>A
• NG_011619.1:g.15468G>A
• NG_021409.2:g.722289C>T
• NM_001099679.2:c.27G>A
• NM_001365068.1:c.2806+28002C>TMANE SELECT
• NM_001365069.1:c.2794+28002C>T
• NM_001379048.1:c.27G>A
• NM_001379049.1:c.27G>A
• NM_001379050.1:c.27G>A
• NM_012210.4:c.27G>AMANE SELECT
• NM_014010.5:c.2653+28002C>T
• NP_001093149.1:p.Leu9=
• NP_001365977.1:p.Leu9=
• NP_001365978.1:p.Leu9=
• NP_001365979.1:p.Leu9=
• NP_036342.2:p.Leu9=
• NP_036342.2:p.Leu9=
• LRG_211t1:c.27G>A
• LRG_211:g.15468G>A
• LRG_211p1:p.Leu9=
• NC_000009.11:g.119460048G>A
• NM_012210.3:c.27G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001365068.1:c.2806+28002C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001365069.1:c.2794+28002C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_014010.5:c.2653+28002C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001099679.2:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001379048.1:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001379049.1:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001379050.1:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_012210.4:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]