Product Details

SNP ID

rs1260658

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:109099022 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGAATGGAGGAAGTGCCATTTACT[A/G]TTATGGGAAAATCTGCAGATTTGTG

Phenotype

MIM: 606103

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CEP57L1 PubMed Links

Additional Information

For this assay, SNP(s) [rs75861829] are located under a primer 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

CEP57L1

Gene Name

centrosomal protein 57 like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001083535.1		Intron			NP_001077004.1
NM_001271852.1		Intron			NP_001258781.1
NM_001271853.1		Intron			NP_001258782.1
NM_173830.4		Intron			NP_776191.1
XM_005266935.4		Intron			XP_005266992.3
XM_005266936.4		Intron			XP_005266993.3
XM_005266937.4		Intron			XP_005266994.3
XM_005266938.4		Intron			XP_005266995.3
XM_006715462.3		Intron			XP_006715525.1
XM_011535759.2		Intron			XP_011534061.1
XM_011535762.2		Intron			XP_011534064.1
XM_011535763.2		Intron			XP_011534065.2
XM_017010764.1		Intron			XP_016866253.1
XM_017010765.1		Intron			XP_016866254.1
XM_017010767.1		Intron			XP_016866256.1
XM_017010768.1		Intron			XP_016866257.1
XM_017010769.1		Intron			XP_016866258.1
XM_017010770.1		Intron			XP_016866259.1
XM_017010771.1		Intron			XP_016866260.1
XM_017010772.1		Intron			XP_016866261.1

Gene

SESN1

Gene Name

sestrin 1

There are no transcripts associated with this gene.

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