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ACACCGCGTCCCACTGACATTAACT[A/G]GCACTGGAAACTCCACCTCACTTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606526 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MLPH 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
|
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
|
MLPH - melanophilin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042467.2 | Intron | NP_001035932.1 | ||||
NM_001281473.1 | Intron | NP_001268402.1 | ||||
NM_001281474.1 | Intron | NP_001268403.1 | ||||
NM_024101.6 | Intron | NP_077006.1 | ||||
XM_006712737.1 | Intron | XP_006712800.1 | ||||
XM_006712739.1 | Intron | XP_006712802.1 | ||||
XM_006712740.1 | Intron | XP_006712803.1 | ||||
XM_011511812.1 | Intron | XP_011510114.1 | ||||
XM_017004893.1 | Intron | XP_016860382.1 | ||||
XM_017004894.1 | Intron | XP_016860383.1 |