Product Details

SNP ID

rs201628798

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:2771523 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTGGGTCCGTCTTGGGGTTCCCT[C/T]GTTGAACATGCTGTCAAACCAGGAC

Phenotype

MIM: 606032 MIM: 600787

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SRRM2 PubMed Links

Additional Information

For this assay, SNP(s) [rs4036] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SRRM2

Gene Name

serine/arginine repetitive matrix 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016333.3	881	Intron			NP_057417.3
XM_005255226.1	881	Intron			XP_005255283.1
XM_006720874.3	881	Intron			XP_006720937.1

Gene

TCEB2

Gene Name

transcription elongation factor B subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007108.3	881	UTR 3			NP_009039.1
NM_207013.2	881	Silent Mutation	ACA,ACG	T145T	NP_996896.1

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