Product Details

SNP ID
rs17225497
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:63768352 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGTAAAAAACGTCAGTTAGCTGA[G/T]ATTAAGCCTTCATGTTGTAAACCTC
Phenotype
MIM: 608442
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SYNE2 PubMed Links

Gene Details

Gene
SYNE2
Gene Name
spectrin repeat containing nuclear envelope protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015180.4 Intron NP_055995.4
NM_182910.2 Intron NP_878914.1
NM_182913.2 Intron NP_878917.1
NM_182914.2 Intron NP_878918.2
XM_005267454.1 Intron XP_005267511.1
XM_005267456.1 Intron XP_005267513.1
XM_005267457.1 Intron XP_005267514.1
XM_005267458.1 Intron XP_005267515.1
XM_005267459.1 Intron XP_005267516.1
XM_011536574.1 Intron XP_011534876.1
XM_011536575.2 Intron XP_011534877.1
XM_011536576.2 Intron XP_011534878.1
XM_011536577.2 Intron XP_011534879.1
XM_011536578.1 Intron XP_011534880.1
XM_011536579.1 Intron XP_011534881.1
XM_011536580.1 Intron XP_011534882.1
XM_011536581.1 Intron XP_011534883.1
XM_011536582.1 Intron XP_011534884.1
XM_011536584.2 Intron XP_011534886.1
XM_017021101.1 Intron XP_016876590.1
XM_017021102.1 Intron XP_016876591.1
XM_017021103.1 Intron XP_016876592.1
XM_017021104.1 Intron XP_016876593.1

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