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AACATGCAAAAAAAATTCCCACCTA[A/G]ACTTTGTCAGTGATTTTGATGGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604280 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PLXNA4 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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PLXNA4 - plexin A4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105543.1 | 9712 | Intron | NP_001099013.1 | |||
NM_020911.1 | 9712 | UTR 3 | NP_065962.1 | |||
NM_181775.3 | 9712 | Intron | NP_861440.2 | |||
XM_005250686.4 | 9712 | UTR 3 | XP_005250743.1 | |||
XM_006716171.3 | 9712 | UTR 3 | XP_006716234.1 | |||
XM_011516676.2 | 9712 | Intron | XP_011514978.1 | |||
XM_017012779.1 | 9712 | UTR 3 | XP_016868268.1 |