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GCCCGGGGCTTATCGCTCTGAGTCA[C/G]AGAAGGAAGAGGGCTTAGTCCATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616312 | ||||||||||||||||||||
Literature Links: |
LEMD2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
LEMD2 - LEM domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143944.1 | 928 | Missense Mutation | TCT,TGT | S,C 197 | NP_001137416.1 | |
NM_181336.3 | 928 | Missense Mutation | TCT,TGT | S,C 499 | NP_851853.1 | |
XM_017010437.1 | 928 | Intron | XP_016865926.1 |