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GTCCAGACACTGATTTGCTGACAGT[A/G]GAATGTGAACTCTCTCAAGTCTACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608929 MIM: 605520 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EMILIN3 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
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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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EMILIN3 - elastin microfibril interfacer 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052846.1 | 2788 | UTR 3 | NP_443078.1 |
LPIN3 - lipin 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301860.1 | 2788 | Intron | NP_001288789.1 | |||
XM_005260516.2 | 2788 | Intron | XP_005260573.1 | |||
XM_006723863.2 | 2788 | Intron | XP_006723926.1 | |||
XM_011528996.1 | 2788 | Intron | XP_011527298.1 | |||
XM_011528997.2 | 2788 | Intron | XP_011527299.1 | |||
XM_011528998.2 | 2788 | Intron | XP_011527300.1 | |||
XM_011528999.2 | 2788 | Intron | XP_011527301.1 | |||
XM_011529000.1 | 2788 | Intron | XP_011527302.1 | |||
XM_011529001.1 | 2788 | Intron | XP_011527303.1 | |||
XM_011529002.2 | 2788 | Intron | XP_011527304.1 | |||
XM_011529003.1 | 2788 | Intron | XP_011527305.1 | |||
XM_011529004.1 | 2788 | Intron | XP_011527306.1 | |||
XM_011529005.2 | 2788 | Intron | XP_011527307.1 | |||
XM_011529006.2 | 2788 | Intron | XP_011527308.1 | |||
XM_017028020.1 | 2788 | Intron | XP_016883509.1 |