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GGTTCCTCTGCTCAGCCGCTGGATA[A/C]GGATGCCTGAACTTTAATCATCTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 607399 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MCOLN2 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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MCOLN2 - mucolipin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153259.3 | 1820 | UTR 3 | NP_694991.2 | |||
XM_005270719.3 | 1820 | UTR 3 | XP_005270776.1 | |||
XM_006710552.2 | 1820 | UTR 3 | XP_006710615.1 | |||
XM_011541187.2 | 1820 | UTR 3 | XP_011539489.1 | |||
XM_011541188.2 | 1820 | UTR 3 | XP_011539490.1 | |||
XM_017000923.1 | 1820 | Intron | XP_016856412.1 |