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GGATCCAGGCCTCGCTCTCCTCGCT[A/G]ACTCCAACCGCGAGTGCCACGTAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606027 MIM: 607059 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CPSF1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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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CPSF1 - cleavage and polyadenylation specific factor 1 | ||||||
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There are no transcripts associated with this gene. |
SLC39A4 - solute carrier family 39 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001280557.1 | 1675 | Silent Mutation | GTC,GTT | V,V 83 | NP_001267486.1 | |
NM_017767.2 | 1675 | Silent Mutation | GTC,GTT | V,V 556 | NP_060237.2 | |
NM_130849.3 | 1675 | Silent Mutation | GTC,GTT | V,V 581 | NP_570901.2 | |
XM_006716599.1 | 1675 | Silent Mutation | GTC,GTT | V,V 530 | XP_006716662.1 |