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AGTTCAAGTTCAATGCCATGAGAGC[A/G]TAGTGTAGGGGGAATTACCTAAGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 156225 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LAMA2 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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LAMA2 - laminin subunit alpha 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000426.3 | Intron | NP_000417.2 | ||||
NM_001079823.1 | Intron | NP_001073291.1 | ||||
XM_005266981.3 | Intron | XP_005267038.1 | ||||
XM_005266982.3 | Intron | XP_005267039.1 | ||||
XM_011535820.2 | Intron | XP_011534122.1 | ||||
XM_017010851.1 | Intron | XP_016866340.1 | ||||
XM_017010852.1 | Intron | XP_016866341.1 | ||||
XM_017010853.1 | Intron | XP_016866342.1 |