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ATTAGGATATTGATTATATTTAAAT[A/G]ATTATTTTTCTTTTTCCTTCTGTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602915 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LCA5L 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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LCA5L - LCA5L, lebercilin like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152505.3 | 1992 | Silent Mutation | ATC,ATT | I,I 669 | NP_689718.1 | |
XM_005260926.1 | 1992 | Silent Mutation | ATC,ATT | I,I 669 | XP_005260983.1 | |
XM_006723967.1 | 1992 | Silent Mutation | ATC,ATT | I,I 669 | XP_006724030.1 | |
XM_006723972.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_006724035.1 | |
XM_006723973.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_006724036.1 | |
XM_011529458.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527760.1 | |
XM_011529459.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527761.1 | |
XM_011529460.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527762.1 | |
XM_011529461.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527763.1 | |
XM_011529462.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527764.1 | |
XM_011529463.2 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527765.1 | |
XM_011529464.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527766.1 | |
XM_011529465.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527767.1 | |
XM_011529466.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527768.1 | |
XM_011529467.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527769.1 | |
XM_011529468.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527770.1 | |
XM_011529469.2 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527771.1 | |
XM_011529470.1 | 1992 | Silent Mutation | ATC,ATT | I,I 718 | XP_011527772.1 | |
XM_011529471.1 | 1992 | Silent Mutation | ATC,ATT | I,I 672 | XP_011527773.1 | |
XM_017028274.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_016883763.1 | |
XM_017028275.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_016883764.1 | |
XM_017028276.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_016883765.1 | |
XM_017028277.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_016883766.1 | |
XM_017028278.1 | 1992 | Silent Mutation | ATC,ATT | I,I 539 | XP_016883767.1 |
WRB - tryptophan rich basic protein | ||||||
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There are no transcripts associated with this gene. |
WRB-SH3BGR - WRB-SH3BGR readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317744.1 | 1992 | Intron | NP_001304673.1 |