Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCCGGGGATACTTCACTGGCTGG[C/G]GGCTGAAGTGGCCACGAGACTGTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609694 MIM: 605110 | ||||||||||||||||||||
Literature Links: |
GMIP 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 |
GMIP - GEM interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288998.1 | 2651 | Missense Mutation | CCC,CGC | P,R 838 | NP_001275927.1 | |
NM_001288999.1 | 2651 | Missense Mutation | CCC,CGC | P,R 841 | NP_001275928.1 | |
NM_016573.3 | 2651 | Missense Mutation | CCC,CGC | P,R 867 | NP_057657.2 | |
XM_005259927.2 | 2651 | Missense Mutation | CCC,CGC | P,R 864 | XP_005259984.1 | |
XM_011528048.2 | 2651 | Missense Mutation | CCC,CGC | P,R 746 | XP_011526350.1 | |
XM_017026861.1 | 2651 | Missense Mutation | CCC,GCC | P,A 882 | XP_016882350.1 | |
XM_017026862.1 | 2651 | Intron | XP_016882351.1 |
LPAR2 - lysophosphatidic acid receptor 2 | ||||||
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There are no transcripts associated with this gene. |