Search Thermo Fisher Scientific
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TTGACACGATGAACATGTTGTGTCT[C/T]TAGGCCAGTATTCAATCCAGGTCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 120900 | ||||||||||||||||||||
Literature Links: |
C5 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 |
C5 - complement component 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317163.1 | 5133 | Missense Mutation | AAA,AGA | K,R 1656 | NP_001304092.1 | |
NM_001317164.1 | 5133 | Intron | NP_001304093.1 | |||
NM_001735.2 | 5133 | Missense Mutation | AAA,AGA | K,R 1650 | NP_001726.2 | |
XM_011518980.2 | 5133 | Missense Mutation | AAA,AGA | K,R 1655 | XP_011517282.1 | |
XM_017015102.1 | 5133 | Missense Mutation | AAA,AGA | K,R 1655 | XP_016870591.1 | |
XM_017015103.1 | 5133 | Missense Mutation | AAA,AGA | K,R 1534 | XP_016870592.1 | |
XM_017015104.1 | 5133 | Intron | XP_016870593.1 |