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AGCCAATGCCAGGACTCCTGCAATC[A/C]CAGGATGGCAACACCACTTCTAAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612751 MIM: 612896 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LYZL6 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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LYZL6 - lysozyme like 6 | ||||||
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There are no transcripts associated with this gene. |
RDM1 - RAD52 motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001034836.1 | 559 | Missense Mutation | TGG,TGT | W,C 170 | NP_001030008.1 | |
NM_001163120.1 | 559 | Intron | NP_001156592.1 | |||
NM_001163121.1 | 559 | Missense Mutation | TGG,TGT | W,C 170 | NP_001156593.1 | |
NM_001163122.1 | 559 | Missense Mutation | TGG,TGT | W,C 147 | NP_001156594.1 | |
NM_001163124.1 | 559 | Intron | NP_001156596.1 | |||
NM_001163125.1 | 559 | Intron | NP_001156597.1 | |||
NM_001163130.1 | 559 | Missense Mutation | TGG,TGT | W,C 147 | NP_001156602.1 | |
NM_145654.3 | 559 | Missense Mutation | TGG,TGT | W,C 170 | NP_663629.1 | |
XM_011524509.2 | 559 | Missense Mutation | TGG,TGT | W,C 170 | XP_011522811.1 | |
XM_011524510.2 | 559 | Intron | XP_011522812.1 |