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TTCCTGGGAATTCTGATTTTCCAAA[A/G]TGCTTCCCAAAATGTAGTTCTGGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614106 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MLIP 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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
MLIP - muscular LMNA-interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281746.1 | Intron | NP_001268675.1 | ||||
NM_001281747.1 | Intron | NP_001268676.1 | ||||
NM_138569.2 | Intron | NP_612636.2 | ||||
XM_005249476.4 | Intron | XP_005249533.1 | ||||
XM_005249478.4 | Intron | XP_005249535.1 | ||||
XM_005249480.4 | Intron | XP_005249537.1 | ||||
XM_006715245.3 | Intron | XP_006715308.2 | ||||
XM_017011465.1 | Intron | XP_016866954.1 | ||||
XM_017011466.1 | Intron | XP_016866955.1 | ||||
XM_017011467.1 | Intron | XP_016866956.1 | ||||
XM_017011468.1 | Intron | XP_016866957.1 | ||||
XM_017011469.1 | Intron | XP_016866958.1 | ||||
XM_017011470.1 | Intron | XP_016866959.1 |