Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCAGCTCTGTAGGCCGCCCATCCC[A/G]CTCATGATCATAGCTGAGGGAGCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609552 | ||||||||||||||||||||
Literature Links: |
FER1L5 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 |
FER1L5 - fer-1 like family member 5 | ||||||
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There are no transcripts associated with this gene. |
LMAN2L - lectin, mannose binding 2 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142292.1 | 501 | Missense Mutation | CGG,TGG | R,W 201 | NP_001135764.1 | |
NM_001322346.1 | 501 | Missense Mutation | CGG,TGG | R,W 56 | NP_001309275.1 | |
NM_001322347.1 | 501 | Missense Mutation | CGG,TGG | R,W 63 | NP_001309276.1 | |
NM_001322350.1 | 501 | Missense Mutation | CGG,TGG | R,W 52 | NP_001309279.1 | |
NM_001322351.1 | 501 | Missense Mutation | CGG,TGG | R,W 45 | NP_001309280.1 | |
NM_001322352.1 | 501 | Missense Mutation | CGG,TGG | R,W 63 | NP_001309281.1 | |
NM_001322354.1 | 501 | Missense Mutation | CGG,TGG | R,W 56 | NP_001309283.1 | |
NM_001322355.1 | 501 | Missense Mutation | CGG,TGG | R,W 45 | NP_001309284.1 | |
NM_001322356.1 | 501 | Missense Mutation | CGG,TGG | R,W 45 | NP_001309285.1 | |
NM_030805.3 | 501 | Missense Mutation | CGG,TGG | R,W 190 | NP_110432.1 |