Product Details

SNP ID
rs144446070
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:48356979 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATACTGTTTATATACACATATATT[C/T]TACCCTGCAACTAATGTCACTTCAG
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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