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- SNP ID:
- rs199527404
- Gene
-
ZCCHC6 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.9: 86323826 - 86323826 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
ATACATGTAATTGCATTCAGAGGCT[G/T]TAGAAGGCTGGATTTTGTAATTTTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613467
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Literature Links: |
ZCCHC6 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 |
| ZCCHC6 - zinc finger CCHC-type containing 6 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001185059.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | NP_001171988.1 | |
| NM_001185074.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 519 | NP_001172003.1 | |
| NM_024617.3 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | NP_078893.2 | |
| XM_005252207.3 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_005252264.1 | |
| XM_005252208.2 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_005252265.1 | |
| XM_006717283.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_006717346.1 | |
| XM_011519011.2 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_011517313.1 | |
| XM_011519012.2 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_011517314.1 | |
| XM_011519013.2 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_011517315.1 | |
| XM_011519014.2 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_011517316.1 | |
| XM_011519015.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_011517317.1 | |
| XM_011519016.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_011517318.1 | |
| XM_017015130.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_016870619.1 | |
| XM_017015131.1 | 2741 | Missense Mutation | AAG,CAG | K,Q 642 | XP_016870620.1 | |
| XM_017015132.1 | 2741 | UTR 5 | XP_016870621.1 | |||
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