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AGAAGCTATCTCTTTAACACACTTA[C/G]GGAAAAATCCGAAAACATTTTCTAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616585 | ||||||||||||||||||||
Literature Links: |
FAM192A 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 |
FAM192A - family with sequence similarity 192 member A | ||||||
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There are no transcripts associated with this gene. |
RSPRY1 - ring finger and SPRY domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305163.1 | Intron | NP_001292092.1 | ||||
NM_001305164.1 | Intron | NP_001292093.1 | ||||
NM_001305182.1 | Intron | NP_001292111.1 | ||||
NM_133368.2 | Intron | NP_588609.1 | ||||
XM_005256220.1 | Intron | XP_005256277.1 | ||||
XM_011523427.1 | Intron | XP_011521729.1 | ||||
XM_011523428.1 | Intron | XP_011521730.1 | ||||
XM_011523430.1 | Intron | XP_011521732.1 | ||||
XM_017023844.1 | Intron | XP_016879333.1 |