Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCCTGGCCTGCGCCACCGCGCAGC[A/C]CTACGGCATCGCGGGTGAGGCGGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601757 | ||||||||||||||||||||
Literature Links: |
PEX7 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 |
PEX7 - peroxisomal biogenesis factor 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000288.3 | 562 | Missense Mutation | CAC,CCC | H,P 39 | NP_000279.1 | |
XM_005267019.4 | 562 | Intron | XP_005267076.1 | |||
XM_006715502.1 | 562 | Missense Mutation | CAC,CCC | H,P 39 | XP_006715565.1 | |
XM_017010934.1 | 562 | Missense Mutation | CAC,CCC | H,P 39 | XP_016866423.1 |