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GCAGGTCTCTGCCCCGCGCCCTGCT[C/T]CTGCCGCATTCCTCTCCTGGACTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 608869 | ||||||||||||||||||||
Literature Links: |
LOC100996251 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 |
LOC100996251 - uncharacterized LOC100996251 | ||||||
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There are no transcripts associated with this gene. |
LRIG2 - leucine rich repeats and immunoglobulin like domains 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001312686.1 | 380 | UTR 5 | NP_001299615.1 | |||
NM_014813.2 | 380 | Missense Mutation | TCC,TTC | S,F 48 | NP_055628.1 | |
XM_005271369.2 | 380 | Missense Mutation | TCC,TTC | S,F 48 | XP_005271426.1 | |
XM_017002952.1 | 380 | Intron | XP_016858441.1 |