Product Details

SNP ID
rs200074438
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:21522778 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGTGATGGAAGGCGAACAGCCAG[A/G]GACTAGAGAAAGAGCAGCAATATTC
Phenotype
MIM: 602219
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SALL2 PubMed Links

Gene Details

Gene
SALL2
Gene Name
spalt like transcription factor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291446.1 3245 Intron NP_001278375.1
NM_001291447.1 3245 Intron NP_001278376.1
NM_005407.2 3245 Missense Mutation CCT,TCT P984S NP_005398.2
XM_011537064.1 3245 Intron XP_011535366.1
XM_011537065.1 3245 Intron XP_011535367.1

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