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Search Thermo Fisher Scientific
CGTGGCCGTCATCCTCTACTTTGAC[A/G]TCTACGCCCAGCACCTGGCCTTCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
8 submissions
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Phenotype: |
MIM: 603717 MIM: 604013 MIM: 603456 | ||||||||||||||||||||
Literature Links: |
ATP6V0B 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 |
ATP6V0B - ATPase H+ transporting V0 subunit b | ||||||
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There are no transcripts associated with this gene. |
B4GALT2 - beta-1,4-galactosyltransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005417.2 | 263 | Missense Mutation | ATC,GTC | I,V 34 | NP_001005417.1 | |
NM_003780.4 | 263 | Missense Mutation | ATC,GTC | I,V 34 | NP_003771.1 | |
NM_030587.2 | 263 | Missense Mutation | ATC,GTC | I,V 63 | NP_085076.2 | |
XM_017002716.1 | 263 | Missense Mutation | ATC,GTC | I,V 34 | XP_016858205.1 | |
XM_017002717.1 | 263 | Missense Mutation | ATC,GTC | I,V 34 | XP_016858206.1 |
CCDC24 - coiled-coil domain containing 24 | ||||||
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There are no transcripts associated with this gene. |
DPH2 - DPH2 homolog | ||||||
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There are no transcripts associated with this gene. |