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GCACTGCAGGACGTGTCTCGTTTTA[C/T]CTTTCCATTTCAAGTGCTGGGGGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 146631 MIM: 609950 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ICAM3 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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ICAM3 - intercellular adhesion molecule 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320605.1 | 1781 | Missense Mutation | GAT,GGT | D,G 319 | NP_001307534.1 | |
NM_001320606.1 | 1781 | Missense Mutation | GAT,GGT | D,G 338 | NP_001307535.1 | |
NM_001320608.1 | 1781 | Missense Mutation | GAT,GGT | D,G 154 | NP_001307537.1 | |
NM_002162.4 | 1781 | Missense Mutation | GAT,GGT | D,G 415 | NP_002153.2 |
RAVER1 - ribonucleoprotein, PTB binding 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_133452.2 | 1781 | Intron | NP_597709.2 | |||
XM_011527671.1 | 1781 | Intron | XP_011525973.1 |