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TTCATTGTAATTCTCATATTTGCCT[G/T]TGAAAGCAAATATGAAGCAAATGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613572 | ||||||||||||||||||||
Literature Links: |
GPRC6A 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 |
GPRC6A - G protein-coupled receptor class C group 6 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286354.1 | 2359 | Missense Mutation | AAA,ACA | K,T 597 | NP_001273283.1 | |
NM_001286355.1 | 2359 | Missense Mutation | AAA,ACA | K,T 701 | NP_001273284.1 | |
NM_148963.3 | 2359 | Missense Mutation | AAA,ACA | K,T 772 | NP_683766.2 | |
XM_017010475.1 | 2359 | Missense Mutation | AAA,ACA | K,T 725 | XP_016865964.1 | |
XM_017010476.1 | 2359 | Intron | XP_016865965.1 |