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AATAAGTGATTAAGTTAAAATGGGG[A/T]CCTGTGGATGGGCCCTAACCCAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C7orf71 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 |
C7orf71 - chromosome 7 open reading frame 71 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145531.2 | 3213 | Missense Mutation | ACC,TCC | T,S 3 | NP_001139003.1 | |
NM_001302625.1 | 3213 | UTR 5 | NP_001289554.1 | |||
XM_017012010.1 | 3213 | Missense Mutation | ACC,TCC | T,S 3 | XP_016867499.1 | |
XM_017012011.1 | 3213 | Missense Mutation | ACC,TCC | T,S 3 | XP_016867500.1 | |
XM_017012012.1 | 3213 | Intron | XP_016867501.1 | |||
XM_017012013.1 | 3213 | Intron | XP_016867502.1 | |||
XM_017012014.1 | 3213 | Intron | XP_016867503.1 |