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TTTTATATAAAGTTACCTGTGATTG[G/T]ATGGATGGAGTCGAGTGGAGAGGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605938 MIM: 602259 | ||||||||||||||||||||
Literature Links: |
LOC105372795 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 |
LOC105372795 - uncharacterized LOC105372795 | ||||||
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There are no transcripts associated with this gene. |
PIGP - phosphatidylinositol glycan anchor biosynthesis class P | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320480.1 | 446 | Missense Mutation | NP_001307409.1 | |||
NM_016430.3 | 446 | Missense Mutation | NP_057514.2 | |||
NM_153681.2 | 446 | Missense Mutation | NP_710148.1 | |||
NM_153682.2 | 446 | Missense Mutation | NP_710149.1 | |||
XM_005260990.4 | 446 | Intron | XP_005261047.1 | |||
XM_011529596.2 | 446 | Missense Mutation | XP_011527898.1 | |||
XM_017028364.1 | 446 | Missense Mutation | XP_016883853.1 | |||
XM_017028365.1 | 446 | Missense Mutation | XP_016883854.1 |
TTC3 - tetratricopeptide repeat domain 3 | ||||||
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There are no transcripts associated with this gene. |