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ACTTGGCGAGTCTCATGAGGCACTC[A/G]TCCCTCCACTGCCTCCTGGCAGCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609877 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CRYL1 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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CRYL1 - crystallin lambda 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015974.2 | 815 | Silent Mutation | NP_057058.2 | |||
XM_005266415.3 | 815 | Silent Mutation | XP_005266472.1 | |||
XM_005266416.4 | 815 | Intron | XP_005266473.1 | |||
XM_017020624.1 | 815 | Missense Mutation | XP_016876113.1 |