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SNP ID

rs117194081

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:50126862 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGTTCCTGCCTCTGGCCTGCTGC[C/T]TCCTGTTACCTTTGCTCTAATCTGT

Phenotype

MIM: 610994

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TMEM189 PubMed Links

Gene Details

Gene

TMEM189

Gene Name

transmembrane protein 189

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001162505.1		Intron			NP_001155977.1
NM_199129.2		Intron			NP_954580.1

Gene

TMEM189-UBE2V1

Gene Name

TMEM189-UBE2V1 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_199203.2		Intron			NP_954673.1

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