Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGGGGTGTGGGGTACTTGCCCACA[A/G]AGGCTGGGAAAGGATGATAGGCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 600275 | ||||||||||||||||||||
Literature Links: |
NOTCH2 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 |
NOTCH2 - notch 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001200001.1 | 7433 | Intron | NP_001186930.1 | |||
NM_024408.3 | 7433 | Missense Mutation | TCT,TTT | S,F 2379 | NP_077719.2 | |
XM_005270901.3 | 7433 | Missense Mutation | TCT,TTT | S,F 2340 | XP_005270958.1 | |
XM_011541519.2 | 7433 | Missense Mutation | TCT,TTT | S,F 2375 | XP_011539821.1 | |
XM_011541520.2 | 7433 | Missense Mutation | TCT,TTT | S,F 2340 | XP_011539822.1 | |
XM_017001372.1 | 7433 | Missense Mutation | TCT,TTT | S,F 2363 | XP_016856861.1 | |
XM_017001373.1 | 7433 | Missense Mutation | TCT,TTT | S,F 2340 | XP_016856862.1 |