Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGATGGCGTTCACCTCCTCAGCCA[C/T]GGCTGTCAGCGCGAACTCAAACTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601698 | ||||||||||||||||||||
Literature Links: |
PTPRN2 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 |
PTPRN2 - protein tyrosine phosphatase, receptor type N2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308267.1 | 3137 | Missense Mutation | ATG,GTG | M,V 964 | NP_001295196.1 | |
NM_001308268.1 | 3137 | Missense Mutation | ATG,GTG | M,V 1025 | NP_001295197.1 | |
NM_002847.4 | 3137 | Missense Mutation | ATG,GTG | M,V 1002 | NP_002838.2 | |
NM_130842.3 | 3137 | Missense Mutation | ATG,GTG | M,V 985 | NP_570857.2 | |
NM_130843.3 | 3137 | Missense Mutation | ATG,GTG | M,V 973 | NP_570858.2 | |
XM_011516446.1 | 3137 | Intron | XP_011514748.1 | |||
XM_011516447.2 | 3137 | Intron | XP_011514749.1 | |||
XM_011516448.2 | 3137 | Intron | XP_011514750.1 | |||
XM_011516449.2 | 3137 | Intron | XP_011514751.1 | |||
XM_017012475.1 | 3137 | Missense Mutation | ATG,GTG | M,V 936 | XP_016867964.1 | |
XM_017012476.1 | 3137 | Intron | XP_016867965.1 |