Search Thermo Fisher Scientific
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GCCTGCCGTCCCCCCAACTCACCTG[C/T]GCAGTCCCCTAAGCCTGAGGTGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611289 MIM: 608873 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRG1 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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LRG1 - leucine rich alpha-2-glycoprotein 1 | ||||||
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There are no transcripts associated with this gene. |
SEMA6B - semaphorin 6B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032108.3 | 1997 | Missense Mutation | ACA,GCA | T,A 579 | NP_115484.2 | |
XM_011527639.2 | 1997 | Missense Mutation | ACA,GCA | T,A 585 | XP_011525941.1 | |
XM_011527640.2 | 1997 | Missense Mutation | ACA,GCA | T,A 585 | XP_011525942.1 | |
XM_011527641.1 | 1997 | UTR 3 | XP_011525943.1 |