Product Details
- SNP ID
-
rs142128886
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:128460598 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCAACTCCCCCCTTACATGTTCAC[A/G]TGGATGAGAACACCCCTGTCCACGT
- Phenotype
-
MIM: 602015
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ODF2
PubMed Links
Gene Details
- Gene
- ODF2
- Gene Name
- outer dense fiber of sperm tails 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001242352.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
NP_001229281.1 |
NM_001242353.1 |
772 |
Intron |
|
|
NP_001229282.1 |
NM_001242354.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
NP_001229283.1 |
NM_002540.4 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
NP_002531.3 |
NM_153432.1 |
772 |
Intron |
|
|
NP_702910.1 |
NM_153433.1 |
772 |
Intron |
|
|
NP_702911.1 |
NM_153435.1 |
772 |
Missense Mutation |
ATG,GTG |
M102V |
NP_702913.1 |
NM_153436.1 |
772 |
Intron |
|
|
NP_702914.1 |
NM_153437.2 |
772 |
Intron |
|
|
NP_702915.1 |
NM_153439.1 |
772 |
Intron |
|
|
NP_702917.1 |
NM_153440.1 |
772 |
Intron |
|
|
NP_702918.1 |
XM_005252010.2 |
772 |
Intron |
|
|
XP_005252067.1 |
XM_005252011.2 |
772 |
Intron |
|
|
XP_005252068.1 |
XM_005252012.3 |
772 |
Intron |
|
|
XP_005252069.1 |
XM_005252013.3 |
772 |
Intron |
|
|
XP_005252070.1 |
XM_005252014.3 |
772 |
Intron |
|
|
XP_005252071.1 |
XM_005252017.4 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_005252074.1 |
XM_005252018.2 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_005252075.1 |
XM_005252019.3 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_005252076.1 |
XM_005252022.2 |
772 |
Intron |
|
|
XP_005252079.1 |
XM_005252023.2 |
772 |
Intron |
|
|
XP_005252080.1 |
XM_005252024.3 |
772 |
Intron |
|
|
XP_005252081.1 |
XM_005252026.4 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_005252083.1 |
XM_005252029.2 |
772 |
Intron |
|
|
XP_005252086.1 |
XM_006717126.3 |
772 |
Intron |
|
|
XP_006717189.1 |
XM_011518722.2 |
772 |
Missense Mutation |
ATG,GTG |
M102V |
XP_011517024.1 |
XM_011518723.2 |
772 |
Missense Mutation |
ATG,GTG |
M102V |
XP_011517025.1 |
XM_011518724.2 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_011517026.1 |
XM_011518725.2 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_011517027.1 |
XM_011518726.2 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_011517028.1 |
XM_011518728.2 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_011517030.1 |
XM_011518729.2 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_011517031.1 |
XM_011518730.2 |
772 |
Missense Mutation |
ATG,GTG |
M102V |
XP_011517032.1 |
XM_011518731.2 |
772 |
Missense Mutation |
ATG,GTG |
M102V |
XP_011517033.1 |
XM_011518732.2 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_011517034.1 |
XM_011518733.2 |
772 |
Missense Mutation |
ATG,GTG |
M102V |
XP_011517035.1 |
XM_011518744.1 |
772 |
Intron |
|
|
XP_011517046.1 |
XM_017014764.1 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_016870253.1 |
XM_017014765.1 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_016870254.1 |
XM_017014766.1 |
772 |
Intron |
|
|
XP_016870255.1 |
XM_017014767.1 |
772 |
Missense Mutation |
ATG,GTG |
M58V |
XP_016870256.1 |
XM_017014768.1 |
772 |
Intron |
|
|
XP_016870257.1 |
XM_017014769.1 |
772 |
Intron |
|
|
XP_016870258.1 |
XM_017014770.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870259.1 |
XM_017014771.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870260.1 |
XM_017014772.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870261.1 |
XM_017014773.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870262.1 |
XM_017014774.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870263.1 |
XM_017014775.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870264.1 |
XM_017014776.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870265.1 |
XM_017014777.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870266.1 |
XM_017014778.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870267.1 |
XM_017014779.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870268.1 |
XM_017014780.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870269.1 |
XM_017014781.1 |
772 |
Missense Mutation |
ATG,GTG |
M14V |
XP_016870270.1 |
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