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TTCAAGAACATTAGTAACATTTTTT[C/T]TTAGATATTTCTCCTAATACAATGA
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
19 submissions
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Phenotype: |
MIM: 601196 | ||||||||||||||||||||||||||||||||
Literature Links: |
PRDM2 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
PRDM2 - PR domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007257.2 | 466 | Intron | NP_001007258.1 | |||
NM_001135610.1 | 466 | Intron | NP_001129082.1 | |||
NM_012231.4 | 466 | UTR 5 | NP_036363.2 | |||
NM_015866.4 | 466 | UTR 5 | NP_056950.2 | |||
XM_017002253.1 | 466 | Intron | XP_016857742.1 | |||
XM_017002254.1 | 466 | Intron | XP_016857743.1 | |||
XM_017002255.1 | 466 | Intron | XP_016857744.1 | |||
XM_017002256.1 | 466 | Intron | XP_016857745.1 | |||
XM_017002257.1 | 466 | Intron | XP_016857746.1 | |||
XM_017002258.1 | 466 | Intron | XP_016857747.1 | |||
XM_017002259.1 | 466 | Intron | XP_016857748.1 | |||
XM_017002260.1 | 466 | Intron | XP_016857749.1 | |||
XM_017002261.1 | 466 | Intron | XP_016857750.1 | |||
XM_017002262.1 | 466 | Intron | XP_016857751.1 | |||
XM_017002263.1 | 466 | Intron | XP_016857752.1 | |||
XM_017002264.1 | 466 | Intron | XP_016857753.1 |
Set Membership: |
HapMap |