Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATAATGTTAAAGCCATGTTTCTCA[A/C]AGTCCCGAGCTCCACGTAAACTGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 600259 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PMS2 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
PMS2 - PMS1 homolog 2, mismatch repair system component | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000535.6 | Intron | NP_000526.2 | ||||
NM_001322003.1 | Intron | NP_001308932.1 | ||||
NM_001322004.1 | Intron | NP_001308933.1 | ||||
NM_001322005.1 | Intron | NP_001308934.1 | ||||
NM_001322006.1 | Intron | NP_001308935.1 | ||||
NM_001322007.1 | Intron | NP_001308936.1 | ||||
NM_001322008.1 | Intron | NP_001308937.1 | ||||
NM_001322009.1 | Intron | NP_001308938.1 | ||||
NM_001322010.1 | Intron | NP_001308939.1 | ||||
NM_001322011.1 | Intron | NP_001308940.1 | ||||
NM_001322012.1 | Intron | NP_001308941.1 | ||||
NM_001322013.1 | Intron | NP_001308942.1 | ||||
NM_001322014.1 | Intron | NP_001308943.1 | ||||
NM_001322015.1 | Intron | NP_001308944.1 | ||||
XM_006715744.3 | Intron | XP_006715807.1 | ||||
XM_017012342.1 | Intron | XP_016867831.1 |
Set Membership: |
HapMap |