Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGAACACGTAGGCCAGGATGCGGC[A/G]GTCCAGCTGGAAGGCGATCTCGCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606806 MIM: 612412 | ||||||||||||||||||||
Literature Links: |
FTCD 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 |
FTCD - formimidoyltransferase cyclodeaminase | ||||||
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There are no transcripts associated with this gene. |
SPATC1L - spermatogenesis and centriole associated 1-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142854.1 | 352 | Missense Mutation | CGC,TGC | R,C 205 | NP_001136326.1 | |
NM_032261.4 | 352 | Missense Mutation | CGC,TGC | R,C 51 | NP_115637.3 | |
XM_005261188.4 | 352 | Missense Mutation | CGC,TGC | R,C 205 | XP_005261245.1 | |
XM_011529756.2 | 352 | Missense Mutation | CGC,TGC | R,C 91 | XP_011528058.1 | |
XM_017028480.1 | 352 | Missense Mutation | CGC,TGC | R,C 205 | XP_016883969.1 |