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CAAATAAAGACATTTTTTCAGAGTT[G/T]AGTTCAGCAGGTAAGAGAATTTAAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609803 | ||||||||||||||||||||
Literature Links: |
ANKAR 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 |
ANKAR - ankyrin and armadillo repeat containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144708.3 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | NP_653309.3 | |
XM_011510673.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508975.1 | |
XM_011510674.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508976.1 | |
XM_011510675.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508977.1 | |
XM_011510676.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508978.1 | |
XM_011510677.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508979.1 | |
XM_011510679.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508981.1 | |
XM_011510680.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508982.1 | |
XM_011510681.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508983.1 | |
XM_011510682.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508984.1 | |
XM_011510685.2 | 1165 | Missense Mutation | TTG,TTT | L,F 45 | XP_011508987.1 | |
XM_011510686.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508988.1 | |
XM_011510687.2 | 1165 | Intron | XP_011508989.1 | |||
XM_011510688.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508990.1 | |
XM_011510689.2 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_011508991.1 | |
XM_011510691.2 | 1165 | Intron | XP_011508993.1 | |||
XM_011510692.2 | 1165 | Intron | XP_011508994.1 | |||
XM_011510693.2 | 1165 | Intron | XP_011508995.1 | |||
XM_011510694.2 | 1165 | Intron | XP_011508996.1 | |||
XM_017003413.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_016858902.1 | |
XM_017003414.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_016858903.1 | |
XM_017003415.1 | 1165 | Intron | XP_016858904.1 | |||
XM_017003416.1 | 1165 | UTR 5 | XP_016858905.1 | |||
XM_017003417.1 | 1165 | Missense Mutation | TTG,TTT | L,F 197 | XP_016858906.1 | |
XM_017003418.1 | 1165 | Intron | XP_016858907.1 | |||
XM_017003419.1 | 1165 | Intron | XP_016858908.1 | |||
XM_017003420.1 | 1165 | Intron | XP_016858909.1 |
ASNSD1 - asparagine synthetase domain containing 1 | ||||||
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There are no transcripts associated with this gene. |