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- SNP ID:
- rs140176565
- Gene
-
CCDC191ZDHHC23 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.3: 113965359 - 113965359 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TCCGAAGGGTGATCCAGAGGATCCT[A/C]CTTTAAGAATAAAGAAGGAAAAAAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
CCDC191 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 |
| CCDC191 - coiled-coil domain containing 191 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_020817.1 | 2696 | Missense Mutation | AGG,AGT | R,S 869 | NP_065868.1 | |
| XM_005247681.3 | 2696 | Missense Mutation | AGG,AGT | R,S 548 | XP_005247738.1 | |
| XM_006713715.1 | 2696 | Missense Mutation | AGG,AGT | R,S 856 | XP_006713778.1 | |
| XM_011513051.1 | 2696 | Missense Mutation | AGG,AGT | R,S 827 | XP_011511353.1 | |
| XM_011513052.2 | 2696 | Missense Mutation | AGG,AGT | R,S 807 | XP_011511354.1 | |
| XM_011513053.1 | 2696 | Missense Mutation | AGG,AGT | R,S 784 | XP_011511355.1 | |
| XM_011513054.2 | 2696 | Missense Mutation | AGG,AGT | R,S 784 | XP_011511356.1 | |
| XM_017006956.1 | 2696 | Missense Mutation | AGG,AGT | R,S 847 | XP_016862445.1 | |
| XM_017006957.1 | 2696 | Missense Mutation | AGG,AGT | R,S 784 | XP_016862446.1 | |
| XM_017006958.1 | 2696 | Missense Mutation | AGG,AGT | R,S 784 | XP_016862447.1 | |
| XM_017006959.1 | 2696 | Missense Mutation | AGG,AGT | R,S 469 | XP_016862448.1 | |
| ZDHHC23 - zinc finger DHHC-type containing 23 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001320466.1 | 2696 | Intron | NP_001307395.1 | |||
| NM_001320467.1 | 2696 | Intron | NP_001307396.1 | |||
| NM_001320468.1 | 2696 | Intron | NP_001307397.1 | |||
| NM_173570.4 | 2696 | Intron | NP_775841.2 | |||
| XM_005247269.1 | 2696 | Intron | XP_005247326.1 | |||
| XM_005247270.3 | 2696 | Intron | XP_005247327.1 | |||
| XM_006713562.3 | 2696 | Intron | XP_006713625.1 | |||
| XM_011512618.2 | 2696 | Intron | XP_011510920.1 | |||
| XM_011512619.1 | 2696 | Intron | XP_011510921.1 | |||
| XM_017006084.1 | 2696 | Intron | XP_016861573.1 | |||
| XM_017006085.1 | 2696 | Intron | XP_016861574.1 | |||
| XM_017006086.1 | 2696 | Intron | XP_016861575.1 | |||
| XM_017006087.1 | 2696 | Intron | XP_016861576.1 | |||
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