Search Thermo Fisher Scientific
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GGGAAGCGCGTCGCTCTGGGTCCTG[A/G]CAGAAGGAGGTAAGACCCAGCGCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 608863 | ||||||||||||||||||||
Literature Links: |
PDPN 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 |
PDPN - podoplanin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006624.1 | 335 | Intron | NP_001006625.1 | |||
NM_001006625.1 | 335 | Intron | NP_001006626.1 | |||
NM_006474.4 | 335 | Missense Mutation | ACA,GCA | T,A 96 | NP_006465.3 | |
NM_198389.2 | 335 | Missense Mutation | ACA,GCA | T,A 96 | NP_938203.2 | |
XM_006710295.1 | 335 | Intron | XP_006710358.1 |