ClinVar

NM_170675.5(MEIS2):c.96G>T (p.Pro32=)

Gene:

MEIS2:Meis homeobox 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q14

Genomic location:

• Chr15: 37098116 (on Assembly GRCh38)
• Chr15: 37390317 (on Assembly GRCh37)

Preferred name:

NM_170675.5(MEIS2):c.96G>T (p.Pro32=)

HGVS:

• NC_000015.10:g.37098116C>A
• NG_029108.1:g.8184G>T
• NM_001220482.2:c.96G>T
• NM_002399.4:c.57G>T
• NM_170674.5:c.96G>T
• NM_170675.5:c.96G>TMANE SELECT
• NM_170676.5:c.96G>T
• NM_170677.5:c.96G>T
• NM_172315.3:c.57G>T
• NM_172316.3:c.-146G>T
• NP_001207411.1:p.Pro32=
• NP_002390.1:p.Pro19=
• NP_733774.1:p.Pro32=
• NP_733775.1:p.Pro32=
• NP_733776.1:p.Pro32=
• NP_733777.1:p.Pro32=
• NP_758526.1:p.Pro19=
• NC_000015.9:g.37390317C>A
• NM_170674.4:c.96G>T
• NR_051953.2:n.1179G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1301048671

NCBI 1000 Genomes Browser:

rs1301048671

Molecular consequence:

• NM_172316.3:c.-146G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NR_051953.2:n.1179G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001220482.2:c.96G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_002399.4:c.57G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_170674.5:c.96G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_170675.5:c.96G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_170676.5:c.96G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_170677.5:c.96G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_172315.3:c.57G>T - synonymous variant - [Sequence Ontology: SO:0001819]