Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCCACAAGCCCCAGGGTGAGAGAT[C/T]GATGCCCTGCTTTACCAAATATTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603756 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ABCG2 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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YRI (Yoruba) - Not Available | ||||||
SAS
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Japanese
|
CHB (Han Chinese) - Not Available | ||||||
AFR
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Chinese
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JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ABCG2 - ATP binding cassette subfamily G member 2 (Junior blood group) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257386.1 | 2465 | UTR 3 | NP_001244315.1 | |||
NM_004827.2 | 2465 | Missense Mutation | AAT,GAT | N,D 620 | NP_004818.2 | |
XM_005263354.3 | 2465 | Missense Mutation | AAT,GAT | N,D 620 | XP_005263411.1 | |
XM_005263355.3 | 2465 | Missense Mutation | AAT,GAT | N,D 620 | XP_005263412.1 | |
XM_005263356.3 | 2465 | Missense Mutation | AAT,GAT | N,D 618 | XP_005263413.1 | |
XM_011532420.2 | 2465 | Missense Mutation | AAT,GAT | N,D 620 | XP_011530722.1 | |
XM_017008852.1 | 2465 | Missense Mutation | AAT,GAT | N,D 618 | XP_016864341.1 | |
XM_017008853.1 | 2465 | Missense Mutation | AAT,GAT | N,D 620 | XP_016864342.1 |
Set Membership: |
DME Validated Inventoried |