Product Details

SNP ID
rs11636944
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.15:99107400 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
CATGGAGATTTGACCAGTGGTTATT[G/T]TGACTCTCCAAAAAGGAGTATCTGT
Phenotype
MIM: 606087
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SYNM PubMed Links

Gene Details

Gene
SYNM
Gene Name
synemin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015286.5 Intron NP_056101.5
NM_145728.2 Intron NP_663780.2
XM_017022035.1 Intron XP_016877524.1

View Full Product Details