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CGGGGACGCCGGGGCCCCAAGCTCT[C/T]TTCCCGTCCCCGCGGGGCGCCCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610619 MIM: 612812 MIM: 182309 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
F12 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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F12 - coagulation factor XII | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000505.3 | Intron | NP_000496.2 | ||||
XM_011534462.2 | Intron | XP_011532764.1 |
PFN3 - profilin 3 | ||||||
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There are no transcripts associated with this gene. |
SLC34A1 - solute carrier family 34 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167579.1 | Intron | NP_001161051.1 | ||||
NM_003052.4 | Intron | NP_003043.3 | ||||
XM_005265975.1 | Intron | XP_005266032.1 | ||||
XM_017009773.1 | Intron | XP_016865262.1 | ||||
XM_017009774.1 | Intron | XP_016865263.1 | ||||
XM_017009775.1 | Intron | XP_016865264.1 |