Product Details

SNP ID

rs12459472

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:749190 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGAGTGGGAGGCCAGCCTCAGCC[T/C]GGGCGTGGGACGTCTCCACAGTGCC

Phenotype

MIM: 615289 MIM: 608134

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

MISP PubMed Links

Gene Details

Gene

MISP

Gene Name

mitotic spindle positioning

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173481.3		Intron			NP_775752.1
XM_011527685.2		Intron			XP_011525987.1
XM_011527686.2		Intron			XP_011525988.1

Gene

PALM

Gene Name

paralemmin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040134.1		Intron			NP_001035224.1
NM_002579.2		Intron			NP_002570.2
XM_005259565.4		Intron			XP_005259622.1
XM_005259566.4		Intron			XP_005259623.1
XM_017026850.1		Intron			XP_016882339.1

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