Product Details

SNP ID
rs397257
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.4:48349079 on Build GRCh38
Set Membership
Validated
Context Sequence [VIC/FAM]
AATTTTACTTATTCTTCAGGCACAA[C/T]GCAGATTTTCTTTCCTTTGTGAAAT
Phenotype
MIM: 610492
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLAIN2 PubMed Links

Gene Details

Gene
SLAIN2
Gene Name
SLAIN motif family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020846.1 Intron NP_065897.1
XM_005248121.2 Intron XP_005248178.1

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