Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCGCTGAAGCTCCTTCTGCTCCT[C/T]GCGCCGGGTGCCCCGCTGCTTCTCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616759 | ||||||||||||||||||||
Literature Links: |
NOSIP 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 |
NOSIP - nitric oxide synthase interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270960.1 | 424 | Missense Mutation | NP_001257889.1 | |||
NM_015953.4 | 424 | Missense Mutation | NP_057037.1 | |||
XM_005258964.4 | 424 | Missense Mutation | XP_005259021.1 | |||
XM_006723235.3 | 424 | Missense Mutation | XP_006723298.1 | |||
XM_011527015.2 | 424 | Missense Mutation | XP_011525317.1 | |||
XM_011527017.2 | 424 | Missense Mutation | XP_011525319.1 | |||
XM_017026851.1 | 424 | Missense Mutation | XP_016882340.1 | |||
XM_017026852.1 | 424 | Missense Mutation | XP_016882341.1 |