Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGAGGAGCACGTACCGTATTCTA[A/G]TATCTAACAATTCCTTAATCATTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 608100 | ||||||||||||||||||||
Literature Links: |
NFU1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
NFU1 - NFU1 iron-sulfur cluster scaffold | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002755.2 | 832 | Missense Mutation | ACT,ATT | T,I 179 | NP_001002755.1 | |
NM_001002756.2 | 832 | Missense Mutation | ACT,ATT | T,I 38 | NP_001002756.1 | |
NM_015700.3 | 832 | Missense Mutation | ACT,ATT | T,I 155 | NP_056515.2 | |
XM_017003808.1 | 832 | Intron | XP_016859297.1 |