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TGTGCAGGGTGACCGGCCCCATGAG[C/T]AGATCCAGGTCGTTGAAGAATTCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601464 | ||||||||||||||||||||
Literature Links: |
AFF3 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 |
AFF3 - AF4/FMR2 family member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001025108.1 | 3753 | Silent Mutation | CTA,CTG | L,L 1219 | NP_001020279.1 | |
NM_002285.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1194 | NP_002276.2 | |
XM_005263943.3 | 3753 | Silent Mutation | CTA,CTG | L,L 1194 | XP_005264000.2 | |
XM_005263945.3 | 3753 | Silent Mutation | CTA,CTG | L,L 863 | XP_005264002.1 | |
XM_011511169.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1218 | XP_011509471.1 | |
XM_011511170.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1271 | XP_011509472.1 | |
XM_011511171.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1203 | XP_011509473.1 | |
XM_011511172.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1203 | XP_011509474.1 | |
XM_011511173.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1219 | XP_011509475.1 | |
XM_011511174.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1219 | XP_011509476.1 | |
XM_011511175.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1194 | XP_011509477.1 | |
XM_011511176.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1194 | XP_011509478.1 | |
XM_011511177.2 | 3753 | Silent Mutation | CTA,CTG | L,L 1194 | XP_011509479.1 | |
XM_011511178.2 | 3753 | Silent Mutation | CTA,CTG | L,L 833 | XP_011509480.1 | |
XM_011511179.2 | 3753 | Silent Mutation | CTA,CTG | L,L 832 | XP_011509481.1 | |
XM_017004085.1 | 3753 | Silent Mutation | CTA,CTG | L,L 862 | XP_016859574.1 | |
XM_017004086.1 | 3753 | Silent Mutation | CTA,CTG | L,L 830 | XP_016859575.1 | |
XM_017004087.1 | 3753 | Silent Mutation | CTA,CTG | L,L 829 | XP_016859576.1 |