Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCGCCGAGCTGCGGCTGGACTCGC[A/C]CCCGTGCCTGGAGGTGACGGCGGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 602675 | ||||||||||||||||||||
Literature Links: |
RNPEP 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 |
RNPEP - arginyl aminopeptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319182.1 | 277 | Intron | NP_001306111.1 | |||
NM_001319183.1 | 277 | UTR 5 | NP_001306112.1 | |||
NM_001319184.1 | 277 | UTR 5 | NP_001306113.1 | |||
NM_020216.3 | 277 | Missense Mutation | CAC,CCC | H,P 83 | NP_064601.3 | |
XM_005245421.1 | 277 | Intron | XP_005245478.1 | |||
XM_017002022.1 | 277 | Intron | XP_016857511.1 |