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- SNP ID:
- rs201325200
- Gene
-
C22orf46MEI1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.22: 41703434 - 41703434 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TCTCAGGATCAGAGAGTCTGCATCC[A/G]CTTCATAAGTGTGCTTTTTGGTAAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608797
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Literature Links: |
C22orf46 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 |
| C22orf46 - chromosome 22 open reading frame 46 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| MEI1 - meiotic double-stranded break formation protein 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_152513.3 | 312 | Missense Mutation | CAC,CGC | H,R 93 | NP_689726.3 | |
| XM_011529935.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528237.1 | |
| XM_011529936.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528238.1 | |
| XM_011529937.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528239.1 | |
| XM_011529938.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528240.1 | |
| XM_011529939.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528241.1 | |
| XM_011529940.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528242.1 | |
| XM_011529941.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528243.1 | |
| XM_011529942.2 | 312 | Missense Mutation | CAC,CGC | H,R 29 | XP_011528244.1 | |
| XM_011529943.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528245.1 | |
| XM_011529944.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528246.1 | |
| XM_011529945.2 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528247.1 | |
| XM_011529946.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528248.1 | |
| XM_011529947.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528249.1 | |
| XM_011529948.2 | 312 | Intron | XP_011528250.1 | |||
| XM_011529949.1 | 312 | Intron | XP_011528251.1 | |||
| XM_011529950.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528252.1 | |
| XM_011529952.1 | 312 | Intron | XP_011528254.1 | |||
| XM_011529954.1 | 312 | Intron | XP_011528256.1 | |||
| XM_011529955.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528257.1 | |
| XM_011529956.2 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_011528258.1 | |
| XM_017028633.1 | 312 | Missense Mutation | CAC,CGC | H,R 93 | XP_016884122.1 | |
| XM_017028635.1 | 312 | Intron | XP_016884124.1 | |||
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