Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCATGGTGGCAGTTTGTCTGGCTG[A/T]TGGTAGTATTGCTGTCCTGCAAGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114350 | ||||||||||||||||||||
Literature Links: |
AIF1L 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 |
AIF1L - allograft inflammatory factor 1 like | ||||||
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There are no transcripts associated with this gene. |
NUP214 - nucleoporin 214 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318324.1 | 656 | Missense Mutation | GAT,GTT | D,V 171 | NP_001305253.1 | |
NM_001318325.1 | 656 | Intron | NP_001305254.1 | |||
NM_005085.3 | 656 | Missense Mutation | GAT,GTT | D,V 171 | NP_005076.3 | |
XM_005272216.3 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_005272273.1 | |
XM_005272218.3 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_005272275.1 | |
XM_005272219.3 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_005272276.1 | |
XM_006717292.3 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_006717355.1 | |
XM_011519053.2 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_011517355.1 | |
XM_011519055.2 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_011517357.1 | |
XM_017015167.1 | 656 | Missense Mutation | GAT,GTT | D,V 212 | XP_016870656.1 |