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GGCCATGCTTCAGATTGCCATAGAC[A/G]TTACTTTGGACCAGGACATCTTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
BEND2 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 |
BEND2 - BEN domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184767.1 | 2002 | Silent Mutation | AAC,AAT | N,N 616 | NP_001171696.1 | |
NM_153346.4 | 2002 | Silent Mutation | AAC,AAT | N,N 707 | NP_699177.2 | |
XM_011545447.1 | 2002 | Silent Mutation | AAC,AAT | N,N 721 | XP_011543749.1 | |
XM_017029266.1 | 2002 | Silent Mutation | AAC,AAT | N,N 679 | XP_016884755.1 | |
XM_017029267.1 | 2002 | Silent Mutation | AAC,AAT | N,N 721 | XP_016884756.1 |