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TTGTGTTGCCAAGTAATCTGGGGTT[A/G]TGTTCTAGACATTTTGAATATTATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300212 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RGN 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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RGN - regucalcin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282848.1 | Intron | NP_001269777.1 | ||||
NM_001282849.1 | Intron | NP_001269778.1 | ||||
NM_004683.5 | Intron | NP_004674.1 | ||||
NM_152869.3 | Intron | NP_690608.1 | ||||
XM_006724567.2 | Intron | XP_006724630.1 | ||||
XM_006724568.2 | Intron | XP_006724631.1 | ||||
XM_017029954.1 | Intron | XP_016885443.1 |