Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGCTAAGTGCTCCGGGTCATCAG[A/G]GACCTTCATGCACATGTCCTGCAAG
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 |
---|---|---|
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 |
CRYL1 - crystallin lambda 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015974.2 | 771 | Missense Mutation | CCT,TCT | P,S 289 | NP_057058.2 | |
XM_005266415.3 | 771 | Missense Mutation | CCT,TCT | P,S 235 | XP_005266472.1 | |
XM_005266416.4 | 771 | Intron | XP_005266473.1 | |||
XM_017020624.1 | 771 | Missense Mutation | CCT,TCT | P,S 204 | XP_016876113.1 |