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TCATCTCTGTCTGCCTTCATGCCTC[C/T]GAATAAGTACTCTGTGTATTCAGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602069 | ||||||||||||||||||||
Literature Links: |
NRP1 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 |
NRP1 - neuropilin 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024628.2 | 2955 | Intron | NP_001019799.1 | |||
NM_001024629.2 | 2955 | Intron | NP_001019800.1 | |||
NM_001244972.1 | 2955 | Silent Mutation | TCA,TCG | S,S 915 | NP_001231901.1 | |
NM_001244973.1 | 2955 | Silent Mutation | TCA,TCG | S,S 914 | NP_001231902.1 | |
NM_003873.5 | 2955 | Silent Mutation | TCA,TCG | S,S 921 | NP_003864.4 | |
XM_006717521.1 | 2955 | Silent Mutation | TCA,TCG | S,S 922 | XP_006717584.1 | |
XM_006717522.1 | 2955 | Silent Mutation | TCA,TCG | S,S 905 | XP_006717585.1 | |
XM_006717523.2 | 2955 | Silent Mutation | TCA,TCG | S,S 904 | XP_006717586.1 | |
XM_006717524.1 | 2955 | Silent Mutation | TCA,TCG | S,S 887 | XP_006717587.1 | |
XM_006717525.1 | 2955 | Silent Mutation | TCA,TCG | S,S 886 | XP_006717588.1 | |
XM_006717526.1 | 2955 | Intron | XP_006717589.1 | |||
XM_011519755.2 | 2955 | Intron | XP_011518057.1 | |||
XM_011519756.1 | 2955 | Intron | XP_011518058.1 | |||
XM_017016865.1 | 2955 | Silent Mutation | TCA,TCG | S,S 897 | XP_016872354.1 | |
XM_017016866.1 | 2955 | Silent Mutation | TCA,TCG | S,S 740 | XP_016872355.1 |