Search Thermo Fisher Scientific
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GCCCCGCCCTCACCGATCAGGCAGA[A/G]CCCCTCCTGGGCCCGCGTGACAGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611265 | ||||||||||||||||||||
Literature Links: |
FNDC11 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 |
FNDC11 - fibronectin type III domain containing 11 | ||||||
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There are no transcripts associated with this gene. |
HELZ2 - helicase with zinc finger 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037335.2 | 8705 | Missense Mutation | CTC,TTC | L,F 2605 | NP_001032412.2 | |
NM_033405.3 | 8705 | Missense Mutation | CTC,TTC | L,F 2036 | NP_208384.3 |