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CTCGGTCTTCCAGGGCCTGCTCAGG[A/G]CACTCATGTCCCTGTTTGAAAGTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607974 | ||||||||||||||||||||
Literature Links: |
NETO2 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 |
NETO2 - neuropilin and tolloid like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201477.1 | 1865 | Silent Mutation | TGC,TGT | C,C 484 | NP_001188406.1 | |
NM_018092.4 | 1865 | Silent Mutation | TGC,TGT | C,C 491 | NP_060562.3 | |
XM_006721289.1 | 1865 | Silent Mutation | TGC,TGT | C,C 453 | XP_006721352.1 | |
XM_006721291.1 | 1865 | Silent Mutation | TGC,TGT | C,C 446 | XP_006721354.1 | |
XM_006721292.1 | 1865 | Intron | XP_006721355.1 | |||
XM_017023740.1 | 1865 | Silent Mutation | TGC,TGT | C,C 355 | XP_016879229.1 |