Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCCGCACGCCGCAGCTTCTCCCAG[A/C]AGTAATGGCGATTGCACTGGCGCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609150 MIM: 156535 | ||||||||||||||||||||
Literature Links: |
CXXC1 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 |
CXXC1 - CXXC finger protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001101654.1 | 2253 | Missense Mutation | TGC,TTC | C,F 596 | NP_001095124.1 | |
NM_014593.3 | 2253 | Missense Mutation | TGC,TTC | C,F 592 | NP_055408.2 | |
XM_011525940.2 | 2253 | Missense Mutation | TGC,TTC | C,F 596 | XP_011524242.1 | |
XM_011525941.2 | 2253 | Missense Mutation | TGC,TTC | C,F 471 | XP_011524243.1 | |
XM_017025718.1 | 2253 | Missense Mutation | TGC,TTC | C,F 592 | XP_016881207.1 | |
XM_017025719.1 | 2253 | Missense Mutation | TGC,TTC | C,F 467 | XP_016881208.1 |
MBD1 - methyl-CpG binding domain protein 1 | ||||||
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There are no transcripts associated with this gene. |