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AGAGCCACAACCCGATCTCCGTCCT[G/T]GACAGCCCCTCCAGTGATTGCTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605452 MIM: 613474 | ||||||||||||||||||||
Literature Links: |
ABCB6 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 |
ABCB6 - ATP binding cassette subfamily B member 6 (Langereis blood group) | ||||||
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There are no transcripts associated with this gene. |
ZFAND2B - zinc finger AN1-type containing 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270998.1 | 631 | Missense Mutation | TGG,TTG | W,L 184 | NP_001257927.1 | |
NM_001270999.1 | 631 | Missense Mutation | TGG,TTG | W,L 140 | NP_001257928.1 | |
NM_138802.2 | 631 | Missense Mutation | TGG,TTG | W,L 184 | NP_620157.1 | |
XM_006712285.1 | 631 | Missense Mutation | TGG,TTG | W,L 184 | XP_006712348.1 | |
XM_006712286.3 | 631 | Missense Mutation | TGG,TTG | W,L 184 | XP_006712349.1 | |
XM_017003368.1 | 631 | Missense Mutation | TGG,TTG | W,L 184 | XP_016858857.1 |