Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609377 MIM: 610859 MIM: 607484 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACD PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ACD - adrenocortical dysplasia homolog | ||||||
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There are no transcripts associated with this gene. |
C16orf86 - chromosome 16 open reading frame 86 | ||||||
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There are no transcripts associated with this gene. |
CARMIL2 - capping protein regulator and myosin 1 linker 2 | ||||||
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There are no transcripts associated with this gene. |
ENKD1 - enkurin domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
PARD6A - par-6 family cell polarity regulator alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037281.1 | 915 | Missense Mutation | ATC,GTC | I,V 285 | NP_001032358.1 | |
NM_016948.2 | 915 | Missense Mutation | ATC,GTC | I,V 286 | NP_058644.1 | |
XM_005255977.3 | 915 | Missense Mutation | ATC,GTC | I,V 297 | XP_005256034.1 | |
XM_011523095.2 | 915 | Missense Mutation | ATC,GTC | I,V 296 | XP_011521397.1 | |
XM_011523096.2 | 915 | Missense Mutation | ATC,GTC | I,V 293 | XP_011521398.1 | |
XM_017023261.1 | 915 | Missense Mutation | ATC,GTC | I,V 281 | XP_016878750.1 |
Set Membership: |
HapMap |