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GAGTGAGTACTGCCAGCCGGTCCAG[A/G]AGGACCACTCCACGCCGTCGGCATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613357 MIM: 609795 | ||||||||||||||||||||
Literature Links: |
FIBCD1 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 |
FIBCD1 - fibrinogen C domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145106.1 | 1423 | Missense Mutation | TCC,TTC | S,F 439 | NP_001138578.1 | |
NM_032843.4 | 1423 | Missense Mutation | TCC,TTC | S,F 439 | NP_116232.3 |
QRFP - pyroglutamylated RFamide peptide | ||||||
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There are no transcripts associated with this gene. |