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- SNP ID:
- rs140425896
- Gene
-
ZSWIM4 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 13799722 - 13799722 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
TAACCCACTGGCCCTTCCTACAGGT[G/T]GAGGAGCGGTTCTCCCGGGTGCCTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZSWIM4 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 |
| ZSWIM4 - zinc finger SWIM-type containing 4 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_023072.2 | 156 | Silent Mutation | GTG,GTT | V,V 52 | NP_075560.2 | |
| XM_005260023.3 | 156 | Silent Mutation | GTG,GTT | V,V 52 | XP_005260080.1 | |
| XM_017027153.1 | 156 | Silent Mutation | GTG,GTT | V,V 52 | XP_016882642.1 | |
| XM_017027154.1 | 156 | Silent Mutation | GTG,GTT | V,V 52 | XP_016882643.1 | |
| XM_017027155.1 | 156 | Silent Mutation | GTG,GTT | V,V 52 | XP_016882644.1 | |
| XM_017027156.1 | 156 | Intron | XP_016882645.1 | |||
| XM_017027157.1 | 156 | Silent Mutation | GTG,GTT | V,V 52 | XP_016882646.1 | |
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