Product Details

SNP ID
rs2822697
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.21:14489274 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGAAACAGGTTTGCCTACAAAATTA[C/T]GGACTTCCCATAGGATGTTTCAGTG
Phenotype
MIM: 607978
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SAMSN1 PubMed Links

Gene Details

Gene
SAMSN1
Gene Name
SAM domain, SH3 domain and nuclear localization signals 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256370.1 Intron NP_001243299.1
NM_001286523.1 Intron NP_001273452.1
NM_022136.4 Intron NP_071419.3
XM_011529684.2 Intron XP_011527986.1
XM_011529685.1 Intron XP_011527987.1
XM_011529686.1 Intron XP_011527988.1
XM_017028427.1 Intron XP_016883916.1

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