Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGGCCCTGCCTGCCCTGCCGGCCC[A/G]CACCCGCCACCTTCTGCTGGCCAAC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 173515 | |||||||||||||||||||||||
Literature Links: |
GP9 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
GP9 - glycoprotein IX platelet | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000174.4 | 630 | Missense Mutation | CAC,CGC | H,R 52 | NP_000165.1 | |
XM_005247374.3 | 630 | Missense Mutation | CAC,CGC | H,R 52 | XP_005247431.1 | |
XM_011512701.1 | 630 | Missense Mutation | CAC,CGC | H,R 52 | XP_011511003.1 | |
XM_011512702.1 | 630 | Missense Mutation | CAC,CGC | H,R 52 | XP_011511004.1 |