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- SNP ID:
- rs148338405
- Gene
-
GGNPSMD8SPRED3 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 38385530 - 38385530 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
AAGGGCAGCCAGTGGCGCGCAGCGC[C/G]GGTGTTAGCTGCCCCAGTCTGAGAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609966
MIM: 609293
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Literature Links: |
GGN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
| GGN - gametogenetin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_152657.3 | 1979 | Missense Mutation | CGC,GGC | R,G 578 | NP_689870.3 | |
| XM_005258619.4 | 1979 | Missense Mutation | CGC,GGC | R,G 578 | XP_005258676.1 | |
| XM_011526603.2 | 1979 | Missense Mutation | CGC,GGC | R,G 495 | XP_011524905.1 | |
| XM_017026451.1 | 1979 | Missense Mutation | CGC,GGC | R,G 578 | XP_016881940.1 | |
| PSMD8 - proteasome 26S subunit, non-ATPase 8 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| SPRED3 - sprouty related EVH1 domain containing 3 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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