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GGTGGCTGCGGGCCTGACGTGTCCC[C/T]GAGGCTTTCTTATGCTTCTGGTCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609447 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MZB1 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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MZB1 - marginal zone B and B1 cell specific protein | ||||||
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There are no transcripts associated with this gene. |
PROB1 - proline rich basic protein 1 | ||||||
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There are no transcripts associated with this gene. |
SPATA24 - spermatogenesis associated 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_194296.1 | 600 | Silent Mutation | TCA,TCG | S,S 191 | NP_919272.1 | |
XM_005271916.4 | 600 | Missense Mutation | CAG,CGG | Q,R 200 | XP_005271973.1 | |
XM_011543252.2 | 600 | Missense Mutation | CAG,CGG | Q,R 161 | XP_011541554.1 | |
XM_011543253.2 | 600 | Missense Mutation | CAG,CGG | Q,R 161 | XP_011541555.1 | |
XM_011543254.2 | 600 | Intron | XP_011541556.1 |