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AGCATGTCGCTGCAGAGAATCGTGC[A/G]TGTGTCCCTGGAGCATCCCACCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 607934 MIM: 606755 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PADI1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PADI1 - peptidyl arginine deiminase 1 | ||||||
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There are no transcripts associated with this gene. |
PADI3 - peptidyl arginine deiminase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016233.2 | 63 | Missense Mutation | CAT,CGT | H,R 8 | NP_057317.2 | |
XM_011541571.2 | 63 | Intron | XP_011539873.1 | |||
XM_011541572.2 | 63 | Missense Mutation | CAT,CGT | H,R 8 | XP_011539874.1 | |
XM_017001463.1 | 63 | Intron | XP_016856952.1 |