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ACTTTGTTTTGAGCAAACTGTTCTG[G/T]TGTGGATTCCCTTGGGCTACCTATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601107 | ||||||||||||||||||||
Literature Links: |
ABCC2 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 |
ABCC2 - ATP binding cassette subfamily C member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000392.4 | 321 | Missense Mutation | GTG,TTG | V,L 33 | NP_000383.1 | |
XM_006717630.3 | 321 | Intron | XP_006717693.1 | |||
XM_006717631.3 | 321 | Missense Mutation | GTG,TTG | V,L 33 | XP_006717694.1 | |
XM_011539291.2 | 321 | Missense Mutation | GTG,TTG | V,L 33 | XP_011537593.1 | |
XM_017015675.1 | 321 | Missense Mutation | GTG,TTG | V,L 33 | XP_016871164.1 |