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Search Thermo Fisher Scientific
GTTGGGCCGTAGCCACGAAGTGATC[C/T]GGGCGCTGACGGCCCGTGGCATCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 108745 MIM: 611113 | ||||||||||||||||||||
Literature Links: |
AMDHD2 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 |
AMDHD2 - amidohydrolase domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145815.1 | 689 | Missense Mutation | CGG,TGG | R,W 198 | NP_001139287.1 | |
NM_015944.3 | 689 | Missense Mutation | CGG,TGG | R,W 198 | NP_057028.2 | |
XM_017023262.1 | 689 | Missense Mutation | CGG,TGG | R,W 198 | XP_016878751.1 | |
XM_017023263.1 | 689 | Missense Mutation | CGG,TGG | R,W 198 | XP_016878752.1 | |
XM_017023264.1 | 689 | Missense Mutation | CGG,TGG | R,W 198 | XP_016878753.1 | |
XM_017023265.1 | 689 | Missense Mutation | CGG,TGG | R,W 198 | XP_016878754.1 | |
XM_017023266.1 | 689 | Missense Mutation | CGG,TGG | R,W 35 | XP_016878755.1 | |
XM_017023267.1 | 689 | UTR 5 | XP_016878756.1 |
ATP6V0C - ATPase H+ transporting V0 subunit c | ||||||
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There are no transcripts associated with this gene. |
CEMP1 - cementum protein 1 | ||||||
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There are no transcripts associated with this gene. |
MIR3178 - microRNA 3178 | ||||||
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There are no transcripts associated with this gene. |