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CAGTACTCCGTGGCCTGAAGGAGGC[A/G]GGTAATGTTGTAGCTGTGGGTTCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 605492 | ||||||||||||||||||||
Literature Links: |
LOC105371692 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 |
LOC105371692 - uncharacterized LOC105371692 | ||||||
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There are no transcripts associated with this gene. |
LRRN2 - leucine rich repeat neuronal 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006338.2 | 2214 | Missense Mutation | CGC,TGC | R,C 586 | NP_006329.2 | |
NM_201630.1 | 2214 | Missense Mutation | CGC,TGC | R,C 586 | NP_963924.1 | |
XM_005244827.3 | 2214 | Missense Mutation | CGC,TGC | R,C 586 | XP_005244884.1 | |
XM_011509066.2 | 2214 | Missense Mutation | CGC,TGC | R,C 586 | XP_011507368.1 | |
XM_017000050.1 | 2214 | Missense Mutation | CGC,TGC | R,C 586 | XP_016855539.1 |