ClinVar

NM_016277.5(RAB23):c.90C>T (p.Cys30=)

Gene:

RAB23:RAB23, member RAS oncogene family [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p11.2

Genomic location:

• Chr6: 57210291 (on Assembly GRCh38)
• Chr6: 57075089 (on Assembly GRCh37)

Preferred name:

NM_016277.5(RAB23):c.90C>T (p.Cys30=)

HGVS:

• NC_000006.12:g.57210291G>A
• NG_012170.1:g.16990C>T
• NM_001278666.2:c.90C>T
• NM_001278667.2:c.90C>T
• NM_001278668.2:c.90C>T
• NM_016277.5:c.90C>TMANE SELECT
• NM_183227.3:c.90C>T
• NP_001265595.1:p.Cys30=
• NP_001265596.1:p.Cys30=
• NP_001265597.1:p.Cys30=
• NP_057361.3:p.Cys30=
• NP_899050.1:p.Cys30=
• NC_000006.11:g.57075089G>A
• NR_103822.2:n.268C>T

This HGVS expression did not pass validation

Molecular consequence:

• NR_103822.2:n.268C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001278666.2:c.90C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001278667.2:c.90C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001278668.2:c.90C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_016277.5:c.90C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_183227.3:c.90C>T - synonymous variant - [Sequence Ontology: SO:0001819]