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ATCTGGGGTTTATGCATTTGTAGAT[G/T]GATCTGGATACTATTGATGTAAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615661 MIM: 613295 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PDCD2L 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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PDCD2L - programmed cell death 2 like | ||||||
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There are no transcripts associated with this gene. |
UBA2 - ubiquitin like modifier activating enzyme 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005499.2 | 211 | Missense Mutation | ATG,ATT | M,I 47 | NP_005490.1 | |
XM_005258404.3 | 211 | Missense Mutation | ATG,ATT | M,I 159 | XP_005258461.2 | |
XM_006722962.2 | 211 | Intron | XP_006723025.1 | |||
XM_011526304.2 | 211 | Missense Mutation | ATG,ATT | M,I 159 | XP_011524606.1 | |
XM_017026134.1 | 211 | Missense Mutation | ATG,ATT | M,I 159 | XP_016881623.1 |