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GTGCTCTGGGCCCCATCTTCTGGGG[C/T]GTTCTGTGTGTCATCAGCGCCCTCT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 1603 | Intron | NP_001305133.1 | |||
NM_004560.3 | 1603 | Missense Mutation | NP_004551.2 | |||
XM_005252008.4 | 1603 | Missense Mutation | XP_005252065.1 | |||
XM_005252009.3 | 1603 | Missense Mutation | XP_005252066.1 | |||
XM_006717121.3 | 1603 | Missense Mutation | XP_006717184.1 | |||
XM_017014762.1 | 1603 | Missense Mutation | XP_016870251.1 | |||
XM_017014763.1 | 1603 | Missense Mutation | XP_016870252.1 |