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CTTCCTGCCAGAGGCTGACTCCTGT[C/G]TCACCCGGTTCGCAGTCCCTCACAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603706 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
M1AP 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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M1AP - meiosis 1 associated protein | ||||||
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There are no transcripts associated with this gene. |
SEMA4F - ssemaphorin 4F | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271661.1 | 309 | Missense Mutation | CTC,GTC | L,V 54 | NP_001258590.1 | |
NM_001271662.1 | 309 | Missense Mutation | CTC,GTC | L,V 54 | NP_001258591.1 | |
NM_004263.4 | 309 | Missense Mutation | CTC,GTC | L,V 54 | NP_004254.2 | |
XM_011532475.2 | 309 | Missense Mutation | CTC,GTC | L,V 54 | XP_011530777.1 | |
XM_011532476.2 | 309 | Missense Mutation | CTC,GTC | L,V 54 | XP_011530778.1 | |
XM_011532477.2 | 309 | Missense Mutation | CTC,GTC | L,V 54 | XP_011530779.1 | |
XM_017003172.1 | 309 | Intron | XP_016858661.1 | |||
XM_017003173.1 | 309 | Intron | XP_016858662.1 | |||
XM_017003174.1 | 309 | Intron | XP_016858663.1 |