ClinVar

NM_005343.4(HRAS):c.111+75C>G

Genes:

HRAS:HRas proto-oncogene, GTPase [Gene - OMIM - HGNC]
LRRC56:leucine rich repeat containing 56 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.5

Genomic location:

• Chr11: 534137 (on Assembly GRCh38)
• Chr11: 534137 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.111+75C>G

HGVS:

• NC_000011.10:g.534137G>C
• NG_007666.1:g.6414C>G
• NM_001130442.3:c.111+75C>G
• NM_001318054.2:c.-209+75C>G
• NM_005343.4:c.111+75C>GMANE SELECT
• NM_176795.5:c.111+75C>G
• LRG_506t1:c.111+75C>G
• LRG_506:g.6414C>G
• NC_000011.9:g.534137G>C
• NM_005343.2:c.111+75C>G

This HGVS expression did not pass validation

Links:

dbSNP: rs1228359974

NCBI 1000 Genomes Browser:

rs1228359974

Molecular consequence:

• NM_001130442.3:c.111+75C>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001318054.2:c.-209+75C>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_005343.4:c.111+75C>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_176795.5:c.111+75C>G - intron variant - [Sequence Ontology: SO:0001627]