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TTGTTCTTGACCGTCACGAAGCACA[C/T]GGTGTTGATCATGCTGTTGCTCATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607123 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PROKR2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PROKR2 - prokineticin receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144773.3 | 1238 | Missense Mutation | ATG,GTG | M,V 331 | NP_658986.1 | |
XM_011529159.2 | 1238 | Missense Mutation | ATG,GTG | M,V 295 | XP_011527461.1 | |
XM_017027646.1 | 1238 | Missense Mutation | ATG,GTG | M,V 331 | XP_016883135.1 |