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GACTACCTGCAGGGTTGTCGAGCTG[C/T]TCTGCAGGTAACGAATCCCTGTCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
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Literature Links: |
FAM63A 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 |
FAM63A - family with sequence similarity 63 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040217.2 | 260 | Intron | NP_001035307.1 | |||
NM_001163258.1 | 260 | Intron | NP_001156730.1 | |||
NM_001163259.1 | 260 | Intron | NP_001156731.1 | |||
NM_001163260.1 | 260 | Intron | NP_001156732.1 | |||
NM_001319998.1 | 260 | Intron | NP_001306927.1 | |||
NM_018379.4 | 260 | Intron | NP_060849.2 | |||
XM_005245321.3 | 260 | Intron | XP_005245378.1 | |||
XM_005245325.3 | 260 | Intron | XP_005245382.1 | |||
XM_005245327.3 | 260 | Intron | XP_005245384.1 | |||
XM_005245328.3 | 260 | Intron | XP_005245385.1 | |||
XM_011509757.2 | 260 | Intron | XP_011508059.1 | |||
XM_011509759.2 | 260 | Intron | XP_011508061.1 | |||
XM_017001770.1 | 260 | Intron | XP_016857259.1 | |||
XM_017001771.1 | 260 | Intron | XP_016857260.1 | |||
XM_017001772.1 | 260 | Intron | XP_016857261.1 | |||
XM_017001773.1 | 260 | Intron | XP_016857262.1 | |||
XM_017001774.1 | 260 | Intron | XP_016857263.1 | |||
XM_017001775.1 | 260 | Intron | XP_016857264.1 | |||
XM_017001776.1 | 260 | Intron | XP_016857265.1 | |||
XM_017001777.1 | 260 | Intron | XP_016857266.1 |
PRUNE1 - prune exopolyphosphatase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303229.1 | 260 | UTR 5 | NP_001290158.1 | |||
NM_001303242.1 | 260 | Missense Mutation | GCT,GTT | A,V 11 | NP_001290171.1 | |
NM_001303243.1 | 260 | UTR 5 | NP_001290172.1 | |||
NM_021222.2 | 260 | Missense Mutation | GCT,GTT | A,V 11 | NP_067045.1 | |
XM_005245393.4 | 260 | Missense Mutation | GCT,GTT | A,V 11 | XP_005245450.1 | |
XM_011509832.2 | 260 | UTR 5 | XP_011508134.1 | |||
XM_017001955.1 | 260 | Missense Mutation | GCT,GTT | A,V 11 | XP_016857444.1 | |
XM_017001956.1 | 260 | UTR 5 | XP_016857445.1 | |||
XM_017001957.1 | 260 | UTR 5 | XP_016857446.1 |