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TGCAGCGAGCCGGGCAGCGCAGCCG[C/T]GCTGTTCGGGTTCTGCACGTCGATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608306 | ||||||||||||||||||||
Literature Links: |
SP8 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 |
SP8 - Sp8 transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182700.5 | 917 | Missense Mutation | ACG,GCG | T,A 244 | NP_874359.2 | |
NM_198956.3 | 917 | Missense Mutation | ACG,GCG | T,A 226 | NP_945194.1 |