Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGGCGCGAAACTCCTCGCTGGCTG[A/G]TGCCGCGTTCCTGCTGCTCTGCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 170995 | ||||||||||||||||||||
Literature Links: |
ABCD3 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 |
ABCD3 - ATP binding cassette subfamily D member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122674.1 | 152 | Missense Mutation | GAT,GGT | D,G 17 | NP_001116146.1 | |
NM_002858.3 | 152 | Missense Mutation | GAT,GGT | D,G 17 | NP_002849.1 | |
XM_006710802.2 | 152 | Missense Mutation | GAT,GGT | D,G 17 | XP_006710865.2 | |
XM_011541877.1 | 152 | Intron | XP_011540179.1 | |||
XM_017001952.1 | 152 | Intron | XP_016857441.1 | |||
XM_017001953.1 | 152 | Intron | XP_016857442.1 | |||
XM_017001954.1 | 152 | UTR 5 | XP_016857443.1 |