Product Details

SNP ID
rs149412142
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:51784497 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTGGTCTTCACGGCCAGACCGCCA[C/T]TGAGCATGCTGGTGTACTGGTTCCA
Phenotype
MIM: 607343
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SALL4 PubMed Links

Gene Details

Gene
SALL4
Gene Name
spalt like transcription factor 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318031.1 3221 Missense Mutation AAT,AGT N540S NP_001304960.1
NM_020436.4 3221 Missense Mutation AAT,AGT N977S NP_065169.1
XM_005260467.3 3221 Intron XP_005260524.1
XM_011528921.2 3221 Missense Mutation AAT,AGT N875S XP_011527223.1
XM_011528922.2 3221 Missense Mutation AAT,AGT N875S XP_011527224.1

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