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SNP ID

rs182732022

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:29074775 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCCAACCACTCCCCTGGGCTATG[C/T]GTTAGTCTCCGTCAGCTTGGCCTCT

Phenotype

MIM: 610067 MIM: 609517

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO18A PubMed Links

Gene Details

Gene

MYO18A

Gene Name

myosin XVIIIA

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_078471.3	835	Missense Mutation			NP_510880.2
NM_203318.1	835	Missense Mutation			NP_976063.1

Gene

TIAF1

Gene Name

TGFB1-induced anti-apoptotic factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004740.3	835	UTR 5			NP_004731.2

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