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CACTGTCTTTTCGGAGGATGCCTGG[A/C]AGCCTTGTGTCCATCCGTCCCTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
QRICH2 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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QRICH2 - glutamine rich 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032134.2 | 6023 | Silent Mutation | CTG,CTT | L,L 1611 | NP_115510.1 | |
XM_005257728.3 | 6023 | Silent Mutation | CTG,CTT | L,L 1777 | XP_005257785.1 | |
XM_006722136.3 | 6023 | Silent Mutation | CTG,CTT | L,L 531 | XP_006722199.1 | |
XM_011525344.2 | 6023 | Silent Mutation | CTG,CTT | L,L 1537 | XP_011523646.1 | |
XM_017025206.1 | 6023 | Silent Mutation | CTG,CTT | L,L 1777 | XP_016880695.1 | |
XM_017025207.1 | 6023 | Silent Mutation | CTG,CTT | L,L 1757 | XP_016880696.1 | |
XM_017025208.1 | 6023 | Silent Mutation | CTG,CTT | L,L 455 | XP_016880697.1 |
UBALD2 - UBA like domain containing 2 | ||||||
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There are no transcripts associated with this gene. |