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GTCCAGAAGCCATCACTGCTATCAT[C/T]GTGGTCTTCTCCCTCTTGGCTGCCT
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 | |||
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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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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 | 402 | Silent Mutation | ATC,ATT | I,I 61 | NP_631900.1 | |
NM_174881.3 | 402 | Silent Mutation | ATC,ATT | I,I 61 | NP_777377.1 | |
NM_174882.2 | 402 | Silent Mutation | ATC,ATT | I,I 61 | NP_777378.1 | |
XM_017027471.1 | 402 | Silent Mutation | ATC,ATT | I,I 124 | 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 | 402 | Intron | NP_001277260.1 | |||
NM_024898.3 | 402 | Intron | NP_079174.2 | |||
XM_006722905.2 | 402 | Intron | XP_006722968.2 | |||
XM_006722906.3 | 402 | Intron | XP_006722969.1 | |||
XM_011528318.2 | 402 | Intron | XP_011526620.1 |
SLC25A23 - solute carrier family 25 member 23 | ||||||
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There are no transcripts associated with this gene. |