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GCACAGAGATAGACCCCTGTGCAGA[C/T]GGCCTTAACGGAGGGTGTCACGAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611076 MIM: 608561 | ||||||||||||||||||||
Literature Links: |
NT5DC3 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 |
NT5DC3 - 5'-nucleotidase domain containing 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031701.2 | 6614 | Intron | NP_001026871.1 | |||
XM_011538476.2 | 6614 | Intron | XP_011536778.1 | |||
XM_017019454.1 | 6614 | Intron | XP_016874943.1 |
STAB2 - stabilin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017564.9 | 6614 | Silent Mutation | GAC,GAT | D,D 2129 | NP_060034.9 | |
XM_011538537.2 | 6614 | Silent Mutation | GAC,GAT | D,D 2129 | XP_011536839.1 | |
XM_011538538.2 | 6614 | Silent Mutation | GAC,GAT | D,D 2129 | XP_011536840.1 | |
XM_011538539.2 | 6614 | Silent Mutation | GAC,GAT | D,D 1572 | XP_011536841.1 | |
XM_011538541.2 | 6614 | Silent Mutation | GAC,GAT | D,D 1262 | XP_011536843.1 | |
XM_011538542.2 | 6614 | Silent Mutation | GAC,GAT | D,D 816 | XP_011536844.1 | |
XM_017019585.1 | 6614 | Silent Mutation | GAC,GAT | D,D 2129 | XP_016875074.1 |