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TCTGAGGGTATCAGCTGGGACCTGG[A/C]GTCCTTTGAAGAGCTGGTGGCATCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609737 MIM: 613634 MIM: 608746 | ||||||||||||||||||||
Literature Links: |
CRB3 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 |
CRB3 - crumbs 3, cell polarity complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_139161.4 | 1954 | Intron | NP_631900.1 | |||
NM_174881.3 | 1954 | Intron | NP_777377.1 | |||
NM_174882.2 | 1954 | Intron | NP_777378.1 | |||
XM_017027471.1 | 1954 | Intron | XP_016882960.1 |
DENND1C - DENN domain containing 1C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290331.1 | 1954 | Missense Mutation | GCC,TCC | A,S 594 | NP_001277260.1 | |
NM_024898.3 | 1954 | Missense Mutation | GCC,TCC | A,S 638 | NP_079174.2 | |
XM_006722905.2 | 1954 | Missense Mutation | GCC,TCC | A,S 552 | XP_006722968.2 | |
XM_006722906.3 | 1954 | Missense Mutation | GCC,TCC | A,S 594 | XP_006722969.1 | |
XM_011528318.2 | 1954 | Missense Mutation | GCC,TCC | A,S 594 | XP_011526620.1 |
SLC25A23 - solute carrier family 25 member 23 | ||||||
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There are no transcripts associated with this gene. |