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TGGCATCAGCAGGTACTGCCGTCCT[C/T]GGTAGTTGGACAGCTCGTAGAGGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 123680 MIM: 123690 | ||||||||||||||||||||
Literature Links: |
CRYGC PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
CRYGC - crystallin gamma C | ||||||
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There are no transcripts associated with this gene. |
CRYGD - crystallin gamma D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006891.3 | 535 | Missense Mutation | CAA,CGA | Q,R 140 | NP_008822.2 |
LOC100507443 - uncharacterized LOC100507443 | ||||||
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There are no transcripts associated with this gene. |