ClinVar

NM_001017979.3(RAB28):c.474C>G (p.Val158=)

Gene:

RAB28:RAB28, member RAS oncogene family [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4p15.33

Genomic location:

• Chr4: 13381512 (on Assembly GRCh38)
• Chr4: 13383136 (on Assembly GRCh37)

Preferred name:

NM_001017979.3(RAB28):c.474C>G (p.Val158=)

HGVS:

• NC_000004.12:g.13381512G>C
• NG_033891.1:g.107854C>G
• NM_001017979.3:c.474C>GMANE SELECT
• NM_001159601.2:c.474C>G
• NM_004249.4:c.474C>G
• NP_001017979.1:p.Val158=
• NP_001153073.1:p.Val158=
• NP_004240.2:p.Val158=
• NC_000004.11:g.13383136G>C

This HGVS expression did not pass validation

Links:

dbSNP: rs750653742

NCBI 1000 Genomes Browser:

rs750653742

Molecular consequence:

• NM_001017979.3:c.474C>G - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001159601.2:c.474C>G - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_004249.4:c.474C>G - synonymous variant - [Sequence Ontology: SO:0001819]