ClinVar

NM_002467.6(MYC):c.30+4A>T

Gene:

MYC:MYC proto-oncogene, bHLH transcription factor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q24.21

Genomic location:

• Chr8: 127736627 (on Assembly GRCh38)
• Chr8: 128748873 (on Assembly GRCh37)

Preferred name:

NM_002467.6(MYC):c.30+4A>T

HGVS:

• NC_000008.11:g.127736627A>T
• NG_007161.2:g.6194A>T
• NM_001354870.1:c.30+4A>T
• NM_002467.6:c.30+4A>TMANE SELECT
• LRG_1397t1:c.30+4A>T
• LRG_1397:g.6194A>T
• NC_000008.10:g.128748873A>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001354870.1:c.30+4A>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_002467.6:c.30+4A>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

1