Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCGACGGTCCCGTCCACCACGGCC[C/G]CGTTCTTCAGTAGCAGCACGCTGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605533 | ||||||||||||||||||||
Literature Links: |
NRG3 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 |
NRG3 - neuregulin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010848.3 | 625 | Missense Mutation | CCG,GCG | P,A 199 | NP_001010848.2 | |
NM_001165972.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | NP_001159444.1 | |
NM_001165973.1 | 625 | Intron | NP_001159445.1 | |||
XM_005269444.4 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_005269501.1 | |
XM_011539172.2 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_011537474.1 | |
XM_011539173.2 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_011537475.1 | |
XM_011539175.2 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_011537477.1 | |
XM_011539178.2 | 625 | Intron | XP_011537480.1 | |||
XM_017015573.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871062.1 | |
XM_017015574.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871063.1 | |
XM_017015575.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871064.1 | |
XM_017015576.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871065.1 | |
XM_017015577.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871066.1 | |
XM_017015578.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871067.1 | |
XM_017015579.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871068.1 | |
XM_017015580.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871069.1 | |
XM_017015581.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871070.1 | |
XM_017015582.1 | 625 | Intron | XP_016871071.1 | |||
XM_017015583.1 | 625 | Intron | XP_016871072.1 | |||
XM_017015584.1 | 625 | Missense Mutation | CCG,GCG | P,A 199 | XP_016871073.1 |