Product Details

SNP ID

rs145152970

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:32603275 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCACAGCTGCGCCTCTGCCTCTTT[A/T]ATGACGTTGAGCCCTGCCTGGGGCC

Phenotype

MIM: 615494

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

C21orf59 PubMed Links

Gene Details

Gene

C21orf59

Gene Name

chromosome 21 open reading frame 59

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021254.2	917	Silent Mutation	ATA,ATT	I184I	NP_067077.1

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