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GGTGAGGGGCTGACATTGGGGCTTG[C/G]ACTCCGGGGCTTGGAGCAGGGCAGG
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 |
---|---|---|
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 |
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 |