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CCACGCAAGTTCTCCCTTAGCTGAC[C/T]GCAATCTTGTTTTCTTCCAGGAAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607343 | ||||||||||||||||||||
Literature Links: |
SALL4 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 |
SALL4 - spalt like transcription factor 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318031.1 | 3444 | Silent Mutation | GCA,GCG | A,A 614 | NP_001304960.1 | |
NM_020436.4 | 3444 | Silent Mutation | GCA,GCG | A,A 1051 | NP_065169.1 | |
XM_005260467.3 | 3444 | Intron | XP_005260524.1 | |||
XM_011528921.2 | 3444 | Silent Mutation | GCA,GCG | A,A 949 | XP_011527223.1 | |
XM_011528922.2 | 3444 | Silent Mutation | GCA,GCG | A,A 949 | XP_011527224.1 |