Search Thermo Fisher Scientific
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CCGGTTTGCCCCCCTCTTCCTTGCC[G/T]CCTAAAACACCACTGCTTCCCTGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602219 | ||||||||||||||||||||
Literature Links: |
SALL2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SALL2 - spalt like transcription factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291446.1 | 2950 | Silent Mutation | GGA,GGC | G,G 726 | NP_001278375.1 | |
NM_001291447.1 | 2950 | Silent Mutation | GGA,GGC | G,G 724 | NP_001278376.1 | |
NM_005407.2 | 2950 | Silent Mutation | GGA,GGC | G,G 861 | NP_005398.2 | |
XM_011537064.1 | 2950 | Silent Mutation | GGA,GGC | G,G 861 | XP_011535366.1 | |
XM_011537065.1 | 2950 | Silent Mutation | GGA,GGC | G,G 859 | XP_011535367.1 |