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ACTTCCGTTGTATCTGTTTCTTCCT[A/C]CATGTTTCCGCTGTCTTGTTTGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608134 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PALM 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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PALM - paralemmin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040134.1 | Intron | NP_001035224.1 | ||||
NM_002579.2 | Intron | NP_002570.2 | ||||
XM_005259565.4 | Intron | XP_005259622.1 | ||||
XM_005259566.4 | Intron | XP_005259623.1 | ||||
XM_017026850.1 | Intron | XP_016882339.1 |