Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGCAGGGCTGCCCTGTCTGCCATG[C/G]ATGTGTTGGAGGGGGCCGTGGTGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602337 | ||||||||||||||||||||
Literature Links: |
ROR2 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 |
ROR2 - receptor tyrosine kinase like orphan receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318204.1 | 1550 | Intron | NP_001305133.1 | |||
NM_004560.3 | 1550 | Missense Mutation | TCC,TGC | S,C 882 | NP_004551.2 | |
XM_005252008.4 | 1550 | Missense Mutation | TCC,TGC | S,C 742 | XP_005252065.1 | |
XM_005252009.3 | 1550 | Missense Mutation | TCC,TGC | S,C 481 | XP_005252066.1 | |
XM_006717121.3 | 1550 | Missense Mutation | TCC,TGC | S,C 742 | XP_006717184.1 | |
XM_017014762.1 | 1550 | Missense Mutation | TCC,TGC | S,C 879 | XP_016870251.1 | |
XM_017014763.1 | 1550 | Missense Mutation | TCC,TGC | S,C 742 | XP_016870252.1 |