Product Details

SNP ID
rs138614234
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:21523117 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGCTGATGCCGGACTTGAGCTTC[C/T]CTCCGGTTTGCCCCCCTCTTCCTTG
Phenotype
MIM: 602219
Polymorphism
C/T, 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 2978 Missense Mutation AGA,GGA R736G NP_001278375.1
NM_001291447.1 2978 Missense Mutation AGA,GGA R734G NP_001278376.1
NM_005407.2 2978 Missense Mutation AGA,GGA R871G NP_005398.2
XM_011537064.1 2978 Missense Mutation AGA,GGA R871G XP_011535366.1
XM_011537065.1 2978 Missense Mutation AGA,GGA R869G XP_011535367.1

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