ClinVar

NM_022367.4(SEMA4A):c.300+8G>T

Gene:

SEMA4A:semaphorin 4A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q22

Genomic location:

• Chr1: 156156582 (on Assembly GRCh38)
• Chr1: 156126373 (on Assembly GRCh37)

Preferred name:

NM_022367.4(SEMA4A):c.300+8G>T

HGVS:

• NC_000001.11:g.156156582G>T
• NG_027683.1:g.11639G>T
• NM_001193300.2:c.300+8G>T
• NM_001193301.2:c.300+8G>T
• NM_001193302.2:c.3+8G>T
• NM_001370567.1:c.300+8G>T
• NM_001370568.1:c.3+8G>T
• NM_001370569.1:c.-225+8G>T
• NM_001370571.1:c.-225+8G>T
• NM_022367.4:c.300+8G>TMANE SELECT
• NC_000001.10:g.156126373G>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001193300.2:c.300+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001193301.2:c.300+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001193302.2:c.3+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001370567.1:c.300+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001370568.1:c.3+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001370569.1:c.-225+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001370571.1:c.-225+8G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_022367.4:c.300+8G>T - intron variant - [Sequence Ontology: SO:0001627]