Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGTCTGCACCAGCATCATTCTCT[G/T]TTGCCTCAGCATGTCCAGCACTCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 603271 MIM: 609868 | ||||||||||||||||||||
Literature Links: |
PTPN21 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
PTPN21 - protein tyrosine phosphatase, non-receptor type 21 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007039.3 | 3761 | Missense Mutation | AAG,CAG | K,Q 1146 | NP_008970.2 | |
XM_005267287.2 | 3761 | Missense Mutation | AAG,CAG | K,Q 1146 | XP_005267344.1 | |
XM_006720011.3 | 3761 | Missense Mutation | AAG,CAG | K,Q 1023 | XP_006720074.1 | |
XM_011536367.2 | 3761 | Missense Mutation | AAG,CAG | K,Q 1146 | XP_011534669.1 | |
XM_011536368.2 | 3761 | Missense Mutation | AAG,CAG | K,Q 1023 | XP_011534670.1 | |
XM_011536369.2 | 3761 | Missense Mutation | AAG,CAG | K,Q 942 | XP_011534671.1 | |
XM_017020938.1 | 3761 | Missense Mutation | AAG,CAG | K,Q 1023 | XP_016876427.1 | |
XM_017020939.1 | 3761 | Missense Mutation | AAG,CAG | K,Q 942 | XP_016876428.1 |
SPATA7 - spermatogenesis associated 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040428.3 | 3761 | Intron | NP_001035518.1 | |||
NM_018418.4 | 3761 | Intron | NP_060888.2 | |||
XM_005267851.1 | 3761 | Intron | XP_005267908.1 | |||
XM_005267852.1 | 3761 | Intron | XP_005267909.1 | |||
XM_005267854.1 | 3761 | Intron | XP_005267911.1 | |||
XM_005267855.1 | 3761 | Intron | XP_005267912.1 | |||
XM_006720204.1 | 3761 | Intron | XP_006720267.1 | |||
XM_006720205.1 | 3761 | Intron | XP_006720268.1 | |||
XM_011536951.1 | 3761 | Intron | XP_011535253.1 | |||
XM_011536952.1 | 3761 | Intron | XP_011535254.1 | |||
XM_011536953.1 | 3761 | Intron | XP_011535255.1 | |||
XM_017021452.1 | 3761 | Intron | XP_016876941.1 | |||
XM_017021453.1 | 3761 | Intron | XP_016876942.1 | |||
XM_017021454.1 | 3761 | Intron | XP_016876943.1 | |||
XM_017021455.1 | 3761 | Intron | XP_016876944.1 | |||
XM_017021456.1 | 3761 | Intron | XP_016876945.1 | |||
XM_017021457.1 | 3761 | Intron | XP_016876946.1 |