Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGCTCAAGCGCCACCACGCCCGC[A/G]TGCAGCTGCTGCGTAAGTGCTCCTA
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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319152.1 | 278 | Missense Mutation | ATG,GTG | M,V 68 | NP_001306081.1 | |
NM_001319153.1 | 278 | Missense Mutation | ATG,GTG | M,V 68 | NP_001306082.1 | |
NM_024059.3 | 278 | Missense Mutation | ATG,GTG | M,V 68 | NP_076964.1 | |
XM_011529041.2 | 278 | Missense Mutation | ATG,GTG | M,V 68 | XP_011527343.1 | |
XM_017028060.1 | 278 | Missense Mutation | ATG,GTG | M,V 73 | XP_016883549.1 |
HELZ2 - helicase with zinc finger 2 | ||||||
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There are no transcripts associated with this gene. |
SRMS - src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites | ||||||
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There are no transcripts associated with this gene. |