Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCGTGAATTCCTGTTTGAACATGC[A/G]TGGCAGCCTCATCAAAAGCATTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610914 | ||||||||||||||||||||
Literature Links: |
ENOX1 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 |
ENOX1 - ecto-NOX disulfide-thiol exchanger 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127615.1 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | NP_001121087.1 | |
NM_001242863.1 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | NP_001229792.1 | |
NM_017993.3 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | NP_060463.2 | |
XM_005266439.3 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_005266496.1 | |
XM_011535126.2 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_011533428.1 | |
XM_011535127.2 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_011533429.1 | |
XM_011535128.2 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_011533430.1 | |
XM_011535132.2 | 2456 | Missense Mutation | CGC,TGC | R,C 576 | XP_011533434.1 | |
XM_017020637.1 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_016876126.1 | |
XM_017020638.1 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_016876127.1 | |
XM_017020639.1 | 2456 | Missense Mutation | CGC,TGC | R,C 615 | XP_016876128.1 | |
XM_017020640.1 | 2456 | Missense Mutation | CGC,TGC | R,C 576 | XP_016876129.1 | |
XM_017020641.1 | 2456 | Intron | XP_016876130.1 | |||
XM_017020642.1 | 2456 | Intron | XP_016876131.1 |