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CACTGGGGCCAGTACTGCCGCCGAC[C/G]CCGCTGCTCCTGCTGGTACTGCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600805 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LAMA3 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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LAMA3 - laminin subunit alpha 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000227.4 | 298 | Intron | NP_000218.3 | |||
NM_001127717.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | NP_001121189.2 | |
NM_001127718.2 | 298 | Intron | NP_001121190.2 | |||
NM_001302996.1 | 298 | Silent Mutation | ACC,ACG | T,T 19 | NP_001289925.1 | |
NM_198129.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | NP_937762.2 | |
XM_011525978.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | XP_011524280.1 | |
XM_011525979.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | XP_011524281.1 | |
XM_011525980.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | XP_011524282.1 | |
XM_011525981.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | XP_011524283.1 | |
XM_011525982.2 | 298 | Silent Mutation | ACC,ACG | T,T 19 | XP_011524284.1 | |
XM_017025743.1 | 298 | Intron | XP_016881232.1 | |||
XM_017025744.1 | 298 | Intron | XP_016881233.1 |