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GGCTGTCGGTATGTCGCGACAGAGC[A/C]CCCTGTACAGCTTCTTCCCCAAGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600678 | ||||||||||||||||||||
Literature Links: |
MSH6 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 |
MSH6 - mutS homolog 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000179.2 | 168 | Missense Mutation | ACC,CCC | T,P 6 | NP_000170.1 | |
NM_001281492.1 | 168 | Missense Mutation | ACC,CCC | T,P 6 | NP_001268421.1 | |
NM_001281493.1 | 168 | UTR 5 | NP_001268422.1 | |||
NM_001281494.1 | 168 | Intron | NP_001268423.1 | |||
XM_011532798.1 | 168 | Intron | XP_011531100.1 | |||
XM_011532799.1 | 168 | Intron | XP_011531101.1 |