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GCTGGCAGGGCTGCTTGCACTGCTG[A/C]TGCTGGTAAGACATCTCTCCTCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
|
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Phenotype: |
MIM: 182269 | ||||||||||||||||||||
Literature Links: |
SPRR2C 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 |
SPRR2C - small proline rich protein 2C (pseudogene) | ||||||
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There are no transcripts associated with this gene. |
SPRR2G - small proline rich protein 2G | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014291.3 | 59 | Silent Mutation | NP_001014313.1 | |||
XM_017002177.1 | 59 | Missense Mutation | XP_016857666.1 | |||
XM_017002178.1 | 59 | Missense Mutation | XP_016857667.1 |