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CTTATTTTATCCATATTTTTGCTGT[A/G]AACATTAAGAAATATACCAAGGACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610845 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC35B3 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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SLC35B3 - solute carrier family 35 member B3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142541.2 | 1326 | Missense Mutation | CAC,TAC | H,Y 369 | NP_001136013.1 | |
NM_015948.4 | 1326 | Missense Mutation | CAC,TAC | H,Y 369 | NP_057032.2 | |
XM_005249156.3 | 1326 | Missense Mutation | CAC,TAC | H,Y 371 | XP_005249213.1 | |
XM_005249157.2 | 1326 | Missense Mutation | CAC,TAC | H,Y 369 | XP_005249214.1 | |
XM_005249158.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 337 | XP_005249215.1 | |
XM_006715102.3 | 1326 | Missense Mutation | CAC,TAC | H,Y 369 | XP_006715165.1 | |
XM_006715103.3 | 1326 | Missense Mutation | CAC,TAC | H,Y 340 | XP_006715166.1 | |
XM_011514648.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 337 | XP_011512950.1 | |
XM_011514650.2 | 1326 | Intron | XP_011512952.1 | |||
XM_017010910.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 369 | XP_016866399.1 | |
XM_017010911.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 369 | XP_016866400.1 | |
XM_017010912.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 338 | XP_016866401.1 | |
XM_017010913.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 338 | XP_016866402.1 | |
XM_017010914.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 337 | XP_016866403.1 | |
XM_017010915.1 | 1326 | Missense Mutation | CAC,TAC | H,Y 306 | XP_016866404.1 |