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TCTTCACCCAGGCTTAGGGTGCAGA[G/T]AAGAAAAGAAGTTTATATGGTACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606115 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RPP30 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
RPP30 - ribonuclease P/MRP subunit p30 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001104546.1 | Intron | NP_001098016.1 | ||||
NM_006413.4 | Intron | NP_006404.1 | ||||
XM_011539120.2 | Intron | XP_011537422.1 | ||||
XM_011539121.2 | Intron | XP_011537423.1 | ||||
XM_017015475.1 | Intron | XP_016870964.1 | ||||
XM_017015476.1 | Intron | XP_016870965.1 | ||||
XM_017015477.1 | Intron | XP_016870966.1 | ||||
XM_017015478.1 | Intron | XP_016870967.1 |