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GTCAGCCCAAAATAGGCTGCGAACA[C/T]GTAGAAGTGCCTCAGGTTCATGTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 111700 | ||||||||||||||||||||
Literature Links: |
RHCE 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 |
RHCE - Rh blood group CcEe antigens | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020485.4 | 606 | Missense Mutation | ATG,GTG | M,V 174 | NP_065231.3 | |
NM_138616.3 | 606 | Intron | NP_619522.3 | |||
NM_138617.3 | 606 | Intron | NP_619523.3 | |||
NM_138618.3 | 606 | Missense Mutation | ATG,GTG | M,V 174 | NP_619524.3 | |
XM_005245957.3 | 606 | Missense Mutation | ATG,GTG | M,V 174 | XP_005246014.1 | |
XM_006710810.3 | 606 | Intron | XP_006710873.1 | |||
XM_011541888.2 | 606 | Missense Mutation | ATG,GTG | M,V 134 | XP_011540190.1 | |
XM_011541889.2 | 606 | Missense Mutation | ATG,GTG | M,V 131 | XP_011540191.1 | |
XM_011541890.2 | 606 | Missense Mutation | ATG,GTG | M,V 174 | XP_011540192.1 | |
XM_011541891.2 | 606 | Missense Mutation | ATG,GTG | M,V 118 | XP_011540193.1 | |
XM_017002014.1 | 606 | Missense Mutation | ATG,GTG | M,V 174 | XP_016857503.1 |