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TCCCACCGGGTCTGAAATTTGTGCC[C/T]CCTCCATCCTCCGGTTCTGCTTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607287 MIM: 608239 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LSM7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LSM7 - LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016199.2 | Intron | NP_057283.1 | ||||
XM_017026869.1 | Intron | XP_016882358.1 |
SPPL2B - signal peptide peptidase like 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077238.1 | Intron | NP_001070706.1 | ||||
NM_152988.2 | Intron | NP_694533.1 | ||||
XM_011528138.2 | Intron | XP_011526440.1 | ||||
XM_011528139.1 | Intron | XP_011526441.1 | ||||
XM_011528140.1 | Intron | XP_011526442.1 | ||||
XM_017027016.1 | Intron | XP_016882505.1 | ||||
XM_017027017.1 | Intron | XP_016882506.1 | ||||
XM_017027018.1 | Intron | XP_016882507.1 | ||||
XM_017027019.1 | Intron | XP_016882508.1 |