Product Details

SNP ID

rs2171972

Assay Type

Validated

NCBI dbSNP Submissions

41

Location

Chr.1:243220359 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AAAGGTGGATAATGCTAAATGTGAG[A/G]GTTTTCAGGGCAAACATGAAGAACA

Phenotype

MIM: 613023

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CEP170 PubMed Links

Gene Details

Gene

CEP170

Gene Name

centrosomal protein 170

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042404.1		Intron			NP_001035863.1
NM_001042405.1		Intron			NP_001035864.1
NM_014812.2		Intron			NP_055627.2
XM_006711843.3		Intron			XP_006711906.1
XM_011544334.2		Intron			XP_011542636.1
XM_011544335.2		Intron			XP_011542637.1
XM_011544336.2		Intron			XP_011542638.1
XM_011544337.2		Intron			XP_011542639.1
XM_011544338.2		Intron			XP_011542640.1
XM_011544339.2		Intron			XP_011542641.1
XM_011544340.2		Intron			XP_011542642.1
XM_011544341.2		Intron			XP_011542643.1
XM_011544342.2		Intron			XP_011542644.1
XM_011544343.2		Intron			XP_011542645.1
XM_011544344.2		Intron			XP_011542646.1
XM_017002932.1		Intron			XP_016858421.1
XM_017002933.1		Intron			XP_016858422.1
XM_017002934.1		Intron			XP_016858423.1
XM_017002935.1		Intron			XP_016858424.1
XM_017002936.1		Intron			XP_016858425.1
XM_017002937.1		Intron			XP_016858426.1
XM_017002938.1		Intron			XP_016858427.1
XM_017002939.1		Intron			XP_016858428.1
XM_017002940.1		Intron			XP_016858429.1
XM_017002941.1		Intron			XP_016858430.1
XM_017002942.1		Intron			XP_016858431.1
XM_017002943.1		Intron			XP_016858432.1
XM_017002944.1		Intron			XP_016858433.1
XM_017002945.1		Intron			XP_016858434.1
XM_017002946.1		Intron			XP_016858435.1
XM_017002947.1		Intron			XP_016858436.1
XM_017002948.1		Intron			XP_016858437.1
XM_017002949.1		Intron			XP_016858438.1
XM_017002950.1		Intron			XP_016858439.1
XM_017002951.1		Intron			XP_016858440.1

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