Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTCTGTGGCTGAGCATGGCCCTCC[C/T]AGCCCTGGGCCTGGACCCCTGGAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 607292 | ||||||||||||||||||||
Literature Links: |
SEMA4A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SEMA4A - semaphorin 4A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193300.1 | 309 | Missense Mutation | CCA,CTA | P,L 4 | NP_001180229.1 | |
NM_001193301.1 | 309 | Missense Mutation | CCA,CTA | P,L 4 | NP_001180230.1 | |
NM_001193302.1 | 309 | Intron | NP_001180231.1 | |||
NM_022367.3 | 309 | Missense Mutation | CCA,CTA | P,L 4 | NP_071762.2 | |
XM_011509871.2 | 309 | Intron | XP_011508173.1 | |||
XM_011509872.2 | 309 | Missense Mutation | CCA,CTA | P,L 4 | XP_011508174.1 | |
XM_011509873.2 | 309 | Missense Mutation | CCA,CTA | P,L 4 | XP_011508175.1 | |
XM_011509874.2 | 309 | Intron | XP_011508176.1 | |||
XM_011509875.2 | 309 | Intron | XP_011508177.1 | |||
XM_011509876.2 | 309 | Intron | XP_011508178.1 | |||
XM_011509878.2 | 309 | Intron | XP_011508180.1 | |||
XM_011509879.2 | 309 | Intron | XP_011508181.1 | |||
XM_017002056.1 | 309 | Missense Mutation | CCA,CTA | P,L 4 | XP_016857545.1 | |
XM_017002057.1 | 309 | UTR 5 | XP_016857546.1 |