Product Details
- SNP ID
-
rs75834225
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:56621535 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACATATATCAATGTGATTTCAGGGC[A/C]TTCTCCAGAAGCAAAAGGAGTTGGA
- Phenotype
-
MIM: 616493
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
CCDC66
PubMed Links
Gene Details
- Gene
- CCDC66
- Gene Name
- coiled-coil domain containing 66
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001012506.4 |
2199 |
Missense Mutation |
ATT,CTT |
I888L |
NP_001012524.4 |
NM_001141947.1 |
2199 |
Missense Mutation |
ATT,CTT |
I922L |
NP_001135419.1 |
XM_005265081.3 |
2199 |
Missense Mutation |
ATT,CTT |
I928L |
XP_005265138.1 |
XM_005265082.3 |
2199 |
Missense Mutation |
ATT,CTT |
I921L |
XP_005265139.1 |
XM_005265083.3 |
2199 |
Missense Mutation |
ATT,CTT |
I885L |
XP_005265140.1 |
XM_005265084.3 |
2199 |
Missense Mutation |
ATT,CTT |
I629L |
XP_005265141.1 |
XM_011533614.2 |
2199 |
Missense Mutation |
ATT,CTT |
I895L |
XP_011531916.1 |
XM_011533615.2 |
2199 |
Missense Mutation |
ATT,CTT |
I895L |
XP_011531917.1 |
XM_011533616.2 |
2199 |
Missense Mutation |
ATT,CTT |
I894L |
XP_011531918.1 |
XM_011533617.2 |
2199 |
Missense Mutation |
ATT,CTT |
I894L |
XP_011531919.1 |
XM_011533619.2 |
2199 |
Missense Mutation |
ATT,CTT |
I728L |
XP_011531921.1 |
XM_017006229.1 |
2199 |
Missense Mutation |
ATT,CTT |
I915L |
XP_016861718.1 |
XM_017006230.1 |
2199 |
Missense Mutation |
ATT,CTT |
I895L |
XP_016861719.1 |
XM_017006231.1 |
2199 |
Missense Mutation |
ATT,CTT |
I889L |
XP_016861720.1 |
XM_017006232.1 |
2199 |
Missense Mutation |
ATT,CTT |
I879L |
XP_016861721.1 |
XM_017006233.1 |
2199 |
Missense Mutation |
ATT,CTT |
I872L |
XP_016861722.1 |
XM_017006234.1 |
2199 |
Missense Mutation |
ATT,CTT |
I888L |
XP_016861723.1 |
XM_017006235.1 |
2199 |
Missense Mutation |
ATT,CTT |
I888L |
XP_016861724.1 |
XM_017006236.1 |
2199 |
Missense Mutation |
ATT,CTT |
I629L |
XP_016861725.1 |
XM_017006237.1 |
2199 |
Missense Mutation |
ATT,CTT |
I629L |
XP_016861726.1 |
XM_017006238.1 |
2199 |
Missense Mutation |
ATT,CTT |
I629L |
XP_016861727.1 |
XM_017006239.1 |
2199 |
Missense Mutation |
ATT,CTT |
I629L |
XP_016861728.1 |
XM_017006240.1 |
2199 |
Missense Mutation |
ATT,CTT |
I623L |
XP_016861729.1 |
XM_017006241.1 |
2199 |
Missense Mutation |
ATT,CTT |
I580L |
XP_016861730.1 |
XM_017006242.1 |
2199 |
Missense Mutation |
ATT,CTT |
I580L |
XP_016861731.1 |
XM_017006243.1 |
2199 |
Missense Mutation |
ATT,CTT |
I558L |
XP_016861732.1 |
XM_017006244.1 |
2199 |
Missense Mutation |
ATT,CTT |
I558L |
XP_016861733.1 |
XM_017006245.1 |
2199 |
Missense Mutation |
ATT,CTT |
I496L |
XP_016861734.1 |
- Gene
- FAM208A
- Gene Name
- family with sequence similarity 208 member A
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