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TGACCGTGTGCAGCCCTCATCCCAC[A/G]TGTCAGCGGGACTCCACCTTCCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602121 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DIAPH1 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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DIAPH1 - diaphanous related formin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079812.2 | Intron | NP_001073280.1 | ||||
NM_001314007.1 | Intron | NP_001300936.1 | ||||
NM_005219.4 | Intron | NP_005210.3 | ||||
XM_011537572.2 | Intron | XP_011535874.1 | ||||
XM_011537573.2 | Intron | XP_011535875.1 |