Product Details

SNP ID
rs8101189
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:756709 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGGCTGGACTGTCACTTACGCACCC[C/T]TAAACCAATCACAGAGGTTAGAGAA
Phenotype
MIM: 615289 MIM: 608134
Polymorphism
C/T, 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
There are no transcripts associated with this gene.

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