Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAGGTCTTGAGAGCACCTTGTGGC[A/G]CACCCAGTGTAACTGTGACGGTAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602015 | ||||||||||||||||||||
Literature Links: |
ODF2 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 |
ODF2 - outer dense fiber of sperm tails 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242352.1 | 488 | UTR 5 | NP_001229281.1 | |||
NM_001242353.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | NP_001229282.1 | |
NM_001242354.1 | 488 | UTR 5 | NP_001229283.1 | |||
NM_002540.4 | 488 | UTR 5 | NP_002531.3 | |||
NM_153432.1 | 488 | Missense Mutation | ACA,GCA | T,A 79 | NP_702910.1 | |
NM_153433.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | NP_702911.1 | |
NM_153435.1 | 488 | Missense Mutation | ACA,GCA | T,A 79 | NP_702913.1 | |
NM_153436.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | NP_702914.1 | |
NM_153437.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | NP_702915.1 | |
NM_153439.1 | 488 | Missense Mutation | ACA,GCA | T,A 79 | NP_702917.1 | |
NM_153440.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | NP_702918.1 | |
XM_005252010.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_005252067.1 | |
XM_005252011.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_005252068.1 | |
XM_005252012.3 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252069.1 | |
XM_005252013.3 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252070.1 | |
XM_005252014.3 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252071.1 | |
XM_005252017.4 | 488 | UTR 5 | XP_005252074.1 | |||
XM_005252018.2 | 488 | UTR 5 | XP_005252075.1 | |||
XM_005252019.3 | 488 | UTR 5 | XP_005252076.1 | |||
XM_005252022.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252079.1 | |
XM_005252023.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252080.1 | |
XM_005252024.3 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252081.1 | |
XM_005252026.4 | 488 | UTR 5 | XP_005252083.1 | |||
XM_005252029.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_005252086.1 | |
XM_006717126.3 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_006717189.1 | |
XM_011518722.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_011517024.1 | |
XM_011518723.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_011517025.1 | |
XM_011518724.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_011517026.1 | |
XM_011518725.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_011517027.1 | |
XM_011518726.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_011517028.1 | |
XM_011518728.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_011517030.1 | |
XM_011518729.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_011517031.1 | |
XM_011518730.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_011517032.1 | |
XM_011518731.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_011517033.1 | |
XM_011518732.2 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_011517034.1 | |
XM_011518733.2 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_011517035.1 | |
XM_011518744.1 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_011517046.1 | |
XM_017014764.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_016870253.1 | |
XM_017014765.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_016870254.1 | |
XM_017014766.1 | 488 | Missense Mutation | ACA,GCA | T,A 79 | XP_016870255.1 | |
XM_017014767.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_016870256.1 | |
XM_017014768.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_016870257.1 | |
XM_017014769.1 | 488 | Missense Mutation | ACA,GCA | T,A 35 | XP_016870258.1 | |
XM_017014770.1 | 488 | UTR 5 | XP_016870259.1 | |||
XM_017014771.1 | 488 | UTR 5 | XP_016870260.1 | |||
XM_017014772.1 | 488 | UTR 5 | XP_016870261.1 | |||
XM_017014773.1 | 488 | UTR 5 | XP_016870262.1 | |||
XM_017014774.1 | 488 | UTR 5 | XP_016870263.1 | |||
XM_017014775.1 | 488 | UTR 5 | XP_016870264.1 | |||
XM_017014776.1 | 488 | UTR 5 | XP_016870265.1 | |||
XM_017014777.1 | 488 | UTR 5 | XP_016870266.1 | |||
XM_017014778.1 | 488 | UTR 5 | XP_016870267.1 | |||
XM_017014779.1 | 488 | UTR 5 | XP_016870268.1 | |||
XM_017014780.1 | 488 | UTR 5 | XP_016870269.1 | |||
XM_017014781.1 | 488 | UTR 5 | XP_016870270.1 |