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TTTGAGCTGGCAGCTATCTCCAGGG[G/T]TCTCCTCTAGCACCTCGCCTGGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604184 MIM: 616810 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGDCC3 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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IGDCC3 - immunoglobulin superfamily DCC subclass member 3 | ||||||
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There are no transcripts associated with this gene. |
IGDCC4 - immunoglobulin superfamily DCC subclass member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020962.2 | 3682 | Missense Mutation | NP_066013.1 | |||
XM_011521845.2 | 3682 | Missense Mutation | XP_011520147.1 | |||
XM_011521846.2 | 3682 | Missense Mutation | XP_011520148.1 | |||
XM_011521847.1 | 3682 | Missense Mutation | XP_011520149.1 | |||
XM_017022448.1 | 3682 | Missense Mutation | XP_016877937.1 | |||
XM_017022449.1 | 3682 | Intron | XP_016877938.1 |