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CACGATGATGGGGCAGGAGCGGCCC[C/T]GGTAGCACTTGTTCACCTTCCTGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604139 MIM: 601773 | ||||||||||||||||||||
Literature Links: |
DNAJB2 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 |
DNAJB2 - DnaJ heat shock protein family (Hsp40) member B2 | ||||||
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There are no transcripts associated with this gene. |
MIR153-1 - microRNA 153-1 | ||||||
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There are no transcripts associated with this gene. |
PTPRN - protein tyrosine phosphatase, receptor type N | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199763.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 870 | NP_001186692.1 | |
NM_001199764.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 809 | NP_001186693.1 | |
NM_002846.3 | 2480 | Missense Mutation | CAG,CGG | Q,R 899 | NP_002837.1 | |
XM_011511566.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 826 | XP_011509868.1 | |
XM_017004609.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 900 | XP_016860098.1 | |
XM_017004610.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 871 | XP_016860099.1 | |
XM_017004611.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 827 | XP_016860100.1 | |
XM_017004612.1 | 2480 | Missense Mutation | CAG,CGG | Q,R 797 | XP_016860101.1 |