Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGGATTCCAGGGGGTCCCATCTC[A/G]CCTCGGAGGCCAACTCCAGGTGCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610026 | ||||||||||||||||||||
Literature Links: |
COL22A1 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 |
COL22A1 - collagen type XXII alpha 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152888.2 | 3267 | Silent Mutation | GGC,GGT | G,G 1556 | NP_690848.1 | |
XM_011516883.2 | 3267 | Silent Mutation | GGC,GGT | G,G 1536 | XP_011515185.1 | |
XM_011516884.2 | 3267 | Silent Mutation | GGC,GGT | G,G 1523 | XP_011515186.1 | |
XM_011516885.2 | 3267 | Silent Mutation | GGC,GGT | G,G 1518 | XP_011515187.1 | |
XM_011516886.2 | 3267 | Silent Mutation | GGC,GGT | G,G 1507 | XP_011515188.1 | |
XM_011516887.2 | 3267 | Silent Mutation | GGC,GGT | G,G 1194 | XP_011515189.1 | |
XM_011516888.2 | 3267 | Intron | XP_011515190.1 | |||
XM_011516889.2 | 3267 | Silent Mutation | GGC,GGT | G,G 988 | XP_011515191.1 | |
XM_017013150.1 | 3267 | Silent Mutation | GGC,GGT | G,G 1494 | XP_016868639.1 | |
XM_017013151.1 | 3267 | Silent Mutation | GGC,GGT | G,G 1482 | XP_016868640.1 | |
XM_017013152.1 | 3267 | Silent Mutation | GGC,GGT | G,G 1194 | XP_016868641.1 |