Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATGACGGATGTTCCTGTCGACACA[C/G]GTGTGGCTGCCCGGACTCCTGCTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603747 | ||||||||||||||||||||
Literature Links: |
ABHD16B 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 |
ABHD16B - abhydrolase domain containing 16B | ||||||
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There are no transcripts associated with this gene. |
TPD52L2 - tumor protein D52 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243891.1 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_001230820.1 | |
NM_001243892.1 | 226 | Intron | NP_001230821.1 | |||
NM_001243894.1 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_001230823.1 | |
NM_001243895.1 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_001230824.1 | |
NM_003288.3 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_003279.2 | |
NM_199359.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_955391.1 | |
NM_199360.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_955392.1 | |
NM_199361.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_955393.1 | |
NM_199362.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_955394.1 | |
NM_199363.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | NP_955395.1 | |
XM_011529034.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | XP_011527336.1 | |
XM_011529035.2 | 226 | Missense Mutation | CGT,GGT | R,G 30 | XP_011527337.1 | |
XM_017028038.1 | 226 | Missense Mutation | CGT,GGT | R,G 30 | XP_016883527.1 |