Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGAGTGCAGTCTTCTTTCATCCAG[C/G]GCTCCTCGGCCTTCCTTGGAACCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615904 | ||||||||||||||||||||
Literature Links: |
PXDNL 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 |
PXDNL - peroxidasin like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144651.4 | 5622 | Missense Mutation | CCC,CGC | P,R 1408 | NP_653252.3 | |
XM_005251168.3 | 5622 | Missense Mutation | CCC,CGC | P,R 793 | XP_005251225.1 | |
XM_006716420.3 | 5622 | Missense Mutation | CCC,CGC | P,R 1312 | XP_006716483.1 | |
XM_011517456.2 | 5622 | Missense Mutation | CCC,CGC | P,R 1384 | XP_011515758.1 | |
XM_011517457.2 | 5622 | Missense Mutation | CCC,CGC | P,R 1384 | XP_011515759.1 | |
XM_011517458.2 | 5622 | Missense Mutation | CCC,CGC | P,R 1273 | XP_011515760.1 | |
XM_011517459.2 | 5622 | Intron | XP_011515761.1 | |||
XM_017013041.1 | 5622 | Missense Mutation | CCC,CGC | P,R 1273 | XP_016868530.1 |