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GTCAGGGCCTGTGTGGGACAGTGCT[G/T]TATGCTGTTGAAGAGCTTGGTGTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616243 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIAA0922 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
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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KIAA0922 - KIAA0922 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001131007.1 | Intron | NP_001124479.1 | ||||
NM_015196.3 | Intron | NP_056011.3 | ||||
XM_011531780.1 | Intron | XP_011530082.1 | ||||
XM_011531781.1 | Intron | XP_011530083.1 | ||||
XM_011531783.1 | Intron | XP_011530085.1 | ||||
XM_017007924.1 | Intron | XP_016863413.1 | ||||
XM_017007925.1 | Intron | XP_016863414.1 | ||||
XM_017007926.1 | Intron | XP_016863415.1 | ||||
XM_017007927.1 | Intron | XP_016863416.1 |