Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTCTTTCTTGTCACTTCTAGTTCT[C/T]GCACAGTGAGGACAGGAAAAGTGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605490 | ||||||||||||||||||||
Literature Links: |
CATSPERD 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 |
CATSPERD - cation channel sperm associated auxiliary subunit delta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152784.3 | 429 | Missense Mutation | CGC,TGC | R,C 26 | NP_689997.3 | |
XM_011527885.2 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_011526187.1 | |
XM_011527886.2 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_011526188.1 | |
XM_011527887.2 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_011526189.1 | |
XM_011527888.2 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_011526190.1 | |
XM_011527889.2 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_011526191.1 | |
XM_011527890.2 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_011526192.1 | |
XM_011527891.1 | 429 | Intron | XP_011526193.1 | |||
XM_011527892.1 | 429 | Intron | XP_011526194.1 | |||
XM_017026564.1 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_016882053.1 | |
XM_017026565.1 | 429 | Intron | XP_016882054.1 | |||
XM_017026566.1 | 429 | Missense Mutation | CGC,TGC | R,C 26 | XP_016882055.1 |
LONP1 - lon peptidase 1, mitochondrial | ||||||
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There are no transcripts associated with this gene. |