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Search Thermo Fisher Scientific
CTTGATCATGTCGGCAGTAACGAAG[A/C]CTGAGCTGTACTTCCAGCCTGAAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608342 MIM: 603142 | ||||||||||||||||||||
Literature Links: |
CYB5R2 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 |
CYB5R2 - cytochrome b5 reductase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001302826.1 | 900 | Missense Mutation | GGC,GTC | G,V 226 | NP_001289755.1 | |
NM_001302827.1 | 900 | Missense Mutation | GCT,TCT | A,S 225 | NP_001289756.1 | |
NM_016229.4 | 900 | Missense Mutation | GGC,GTC | G,V 226 | NP_057313.2 | |
XM_005252975.4 | 900 | Missense Mutation | GGC,GTC | G,V 226 | XP_005253032.1 | |
XM_006718251.2 | 900 | Missense Mutation | GGC,GTC | G,V 226 | XP_006718314.1 | |
XM_011520184.2 | 900 | Missense Mutation | GGC,GTC | G,V 286 | XP_011518486.1 | |
XM_011520185.2 | 900 | UTR 3 | XP_011518487.1 | |||
XM_017017920.1 | 900 | Missense Mutation | GGC,GTC | G,V 286 | XP_016873409.1 | |
XM_017017921.1 | 900 | Missense Mutation | GCT,TCT | A,S 253 | XP_016873410.1 | |
XM_017017922.1 | 900 | Missense Mutation | GCT,TCT | A,S 193 | XP_016873411.1 |