Product Details

SNP ID
rs9574102
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:77715896 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCATCCTTTTAGCAATGTCTTTCA[A/G]AAAGAAAAGTTTTTAATTTTGATGA
Phenotype
MIM: 610491
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLAIN1 PubMed Links

Gene Details

Gene
SLAIN1
Gene Name
SLAIN motif family member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040153.3 Intron NP_001035243.2
NM_001242868.1 Intron NP_001229797.1
NM_001242869.1 Intron NP_001229798.1
NM_001242870.1 Intron NP_001229799.1
NM_001242871.1 Intron NP_001229800.1
NM_144595.3 Intron NP_653196.1
XM_011534929.2 Intron XP_011533231.1
XM_011534930.1 Intron XP_011533232.1

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