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SNP ID

rs77864156

Assay Type

Functionally tested

NCBI dbSNP Submissions

24

Location

Chr.1:61688044 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAATTAAGCATCAAAATTCCTACA[C/T]AGTGCCAGAATTTATGCATTCAGAA

Phenotype

MIM: 610080

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TM2D1 PubMed Links

Gene Details

Gene

TM2D1

Gene Name

TM2 domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032027.2		Intron			NP_114416.1

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