Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCTTGATAGGACTTCCTCCCACAG[C/T]AGAGTTGGCTGTTGAAATGCCTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 162341 | ||||||||||||||||||||
Literature Links: |
NMBR 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 |
NMBR - neuromedin B receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324307.1 | 696 | Missense Mutation | TAC,TGC | Y,C 192 | NP_001311236.1 | |
NM_001324308.1 | 696 | Missense Mutation | TAC,TGC | Y,C 192 | NP_001311237.1 | |
NM_002511.3 | 696 | Missense Mutation | TAC,TGC | Y,C 340 | NP_002502.2 | |
XM_011535846.1 | 696 | Missense Mutation | TAC,TGC | Y,C 233 | XP_011534148.1 | |
XM_017010901.1 | 696 | Missense Mutation | TAC,TGC | Y,C 251 | XP_016866390.1 | |
XM_017010902.1 | 696 | Missense Mutation | TAC,TGC | Y,C 192 | XP_016866391.1 |