Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCCCACCGTCGCGGGGGTGGTCAT[A/G]CCGAAACCTGTGGAGACAGGGCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607366 MIM: 609309 | ||||||||||||||||||||
Literature Links: |
HCG2040054 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 |
HCG2040054 - uncharacterized LOC644093 | ||||||
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There are no transcripts associated with this gene. |
KCNK12 - potassium two pore domain channel subfamily K member 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022055.1 | 399 | Silent Mutation | GGC,GGT | G,G 133 | NP_071338.1 |
MSH2 - mutS homolog 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000251.2 | 399 | Intron | NP_000242.1 | |||
NM_001258281.1 | 399 | Intron | NP_001245210.1 | |||
XM_005264332.3 | 399 | Intron | XP_005264389.2 | |||
XM_011532867.1 | 399 | Intron | XP_011531169.1 |