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SNP ID: rs2233160
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:40777489 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATGCAAATACAATCAGCCCAGTGCA[A/G]ACGGCTCGTCTCCGTGGTCTTTGGG
Phenotype: MIM: 601340 MIM: 612945
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MIA PubMed Links

Gene Details

Gene: MIA
Gene Name: melanoma inhibitory activity

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001202553.1	631	UTR 3			NP_001189482.1
NM_006533.3	631	UTR 3			NP_006524.1

Gene: MIA-RAB4B
Gene Name: MIA-RAB4B readthrough (NMD candidate)

There are no transcripts associated with this gene.

Gene: RAB4B
Gene Name: RAB4B, member RAS oncogene family

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016154.4	631	Intron			NP_057238.3

Gene: RAB4B-EGLN2
Gene Name: RAB4B-EGLN2 readthrough (NMD candidate)

There are no transcripts associated with this gene.

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