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GGGAATGCAAGTTGCCGCCACCCTC[C/T]GCCCCCGCCAGCGAGTATTGTCCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
GPATCH1 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 |
GPATCH1 - G-patch domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
WDR88 - WD repeat domain 88 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173479.3 | 138 | Silent Mutation | TCC,TCT | S,S 22 | NP_775750.3 | |
XM_011526449.2 | 138 | Silent Mutation | TCC,TCT | S,S 22 | XP_011524751.1 | |
XM_011526450.2 | 138 | Silent Mutation | TCC,TCT | S,S 22 | XP_011524752.1 | |
XM_017026282.1 | 138 | Silent Mutation | TCC,TCT | S,S 22 | XP_016881771.1 | |
XM_017026283.1 | 138 | Silent Mutation | TCC,TCT | S,S 22 | XP_016881772.1 |