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GACCCGGTGGCCGGGGGGCCCTGTG[C/T]CTCTGTAAGCAGGTTTGCAGGACTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603399 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNK15-AS1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KCNK15-AS1 - KCNK15 antisense RNA 1 (head to head) | ||||||
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There are no transcripts associated with this gene. |
WISP2 - WNT1 inducible signaling pathway protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323369.1 | 468 | Silent Mutation | TGC,TGT | C,C 91 | NP_001310298.1 | |
NM_001323370.1 | 468 | Silent Mutation | TGC,TGT | C,C 91 | NP_001310299.1 | |
NM_003881.3 | 468 | Silent Mutation | TGC,TGT | C,C 91 | NP_003872.1 | |
XM_017028116.1 | 468 | UTR 5 | XP_016883605.1 | |||
XM_017028117.1 | 468 | Silent Mutation | TGC,TGT | C,C 149 | XP_016883606.1 |