Product Details

SNP ID
rs11101822
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:133554319 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCCACCATGTCACTGGTCTACCTG[G/C]TCTGGGAGCCTGTCAAGAAAAGGGA
Phenotype
MIM: 611486
Polymorphism
G/C, Transversion substitution
Allele Nomenclature
Literature Links
SYCE1 PubMed Links

Gene Details

Gene
SYCE1
Gene Name
synaptonemal complex central element protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143763.1 1033 Missense Mutation CCA,GCA P310A NP_001137235.1
NM_001143764.1 1033 Intron NP_001137236.1
NM_130784.2 1033 Missense Mutation CCA,GCA P274A NP_570140.1

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