Product Details

SNP ID

rs2911153

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:81007741 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAACGTTACTTAAAATGGATCTTTT[C/T]GATCATGCGTTCCACAGATCTTGAG

Phenotype

MIM: 611509

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CENPN PubMed Links

Gene Details

Gene

CENPN

Gene Name

centromere protein N

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100624.2		Intron			NP_001094094.2
NM_001100625.2		Intron			NP_001094095.2
NM_001270473.1		Intron			NP_001257402.1
NM_001270474.1		Intron			NP_001257403.1
NM_018455.5		Intron			NP_060925.2
XM_006721236.3		Intron			XP_006721299.1
XM_017023456.1		Intron			XP_016878945.1

Gene

CMC2

Gene Name

C-X9-C motif containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020188.3		Intron			NP_064573.1
XM_017023461.1		Intron			XP_016878950.1
XM_017023462.1		Intron			XP_016878951.1
XM_017023463.1		Intron			XP_016878952.1
XM_017023464.1		Intron			XP_016878953.1
XM_017023465.1		Intron			XP_016878954.1
XM_017023466.1		Intron			XP_016878955.1
XM_017023467.1		Intron			XP_016878956.1
XM_017023468.1		Intron			XP_016878957.1
XM_017023469.1		Intron			XP_016878958.1
XM_017023470.1		Intron			XP_016878959.1

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