ClinVar

NM_003872.3(NRP2):c.2425+9654C>T

Gene:

NRP2:neuropilin 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q33.3

Genomic location:

• Chr2: 205776457 (on Assembly GRCh38)
• Chr2: 206641181 (on Assembly GRCh37)

Preferred name:

NM_003872.3(NRP2):c.2425+9654C>T

HGVS:

• NC_000002.12:g.205776457C>T
• NG_029567.2:g.98958C>T
• NM_003872.3:c.2425+9654C>TMANE SELECT
• NM_018534.4:c.2652C>T
• NM_201266.2:c.2440+9639C>T
• NM_201267.2:c.2637C>T
• NM_201279.2:c.2425+9654C>T
• NP_061004.3:p.Asn884=
• NP_957719.1:p.Asn879=
• NC_000002.11:g.206641181C>T
• NM_201267.1:c.2637C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_003872.3:c.2425+9654C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_201266.2:c.2440+9639C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_201279.2:c.2425+9654C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_018534.4:c.2652C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_201267.2:c.2637C>T - synonymous variant - [Sequence Ontology: SO:0001819]