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TGGCCTTGCATTGCCCCCTGTCTTC[A/G]CAGCGGAGCTTCTTTATCTGACCCG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600700 | |||||||||||||||||||||||
Literature Links: |
FLJ42393 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
FLJ42393 - uncharacterized LOC401105 | ||||||
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There are no transcripts associated with this gene. |
LPP - LIM domain containing preferred translocation partner in lipoma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167671.2 | Intron | NP_001161143.1 | ||||
NM_001167672.2 | Intron | NP_001161144.1 | ||||
NM_005578.4 | Intron | NP_005569.1 | ||||
XM_005247446.4 | Intron | XP_005247503.1 | ||||
XM_005247450.4 | Intron | XP_005247507.1 | ||||
XM_005247451.4 | Intron | XP_005247508.1 | ||||
XM_005247453.2 | Intron | XP_005247510.1 | ||||
XM_011512820.2 | Intron | XP_011511122.1 | ||||
XM_011512823.2 | Intron | XP_011511125.1 | ||||
XM_011512827.2 | Intron | XP_011511129.1 | ||||
XM_011512828.2 | Intron | XP_011511130.1 | ||||
XM_011512831.2 | Intron | XP_011511133.1 | ||||
XM_011512833.2 | Intron | XP_011511135.1 | ||||
XM_011512834.2 | Intron | XP_011511136.1 | ||||
XM_011512836.2 | Intron | XP_011511138.1 | ||||
XM_017006377.1 | Intron | XP_016861866.1 | ||||
XM_017006378.1 | Intron | XP_016861867.1 | ||||
XM_017006379.1 | Intron | XP_016861868.1 | ||||
XM_017006380.1 | Intron | XP_016861869.1 | ||||
XM_017006381.1 | Intron | XP_016861870.1 | ||||
XM_017006382.1 | Intron | XP_016861871.1 |