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CAGATTGAAATCCCAGTGACACCCA[C/T]AGGCCAGTCGGTGCCCAGCTCCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610827 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC107985388 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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LOC107985388 - pre-mRNA-splicing factor cwc22-like | ||||||
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There are no transcripts associated with this gene. |
PCIF1 - PDX1 C-terminal inhibiting factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022104.3 | 688 | Missense Mutation | ACA,ATA | T,I 137 | NP_071387.1 | |
XM_011528980.2 | 688 | Missense Mutation | ACA,ATA | T,I 137 | XP_011527282.1 | |
XM_011528981.2 | 688 | Missense Mutation | ACA,ATA | T,I 137 | XP_011527283.1 | |
XM_017028013.1 | 688 | Missense Mutation | ACA,ATA | T,I 137 | XP_016883502.1 | |
XM_017028014.1 | 688 | UTR 5 | XP_016883503.1 |
ZNF335 - zinc finger protein 335 | ||||||
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There are no transcripts associated with this gene. |