Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGGGCTCGTTTGTAAAAAGAAACT[C/G]TTTTCCCCTGATGAATGAAGAGAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 611342 | ||||||||||||||||||||
Literature Links: |
C9orf64 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 |
C9orf64 - chromosome 9 open reading frame 64 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317997.1 | 847 | Missense Mutation | ACA,AGA | T,R 61 | NP_001304926.1 | |
NM_032307.4 | 847 | Missense Mutation | ACA,AGA | T,R 202 | NP_115683.3 | |
XM_005252271.4 | 847 | Intron | XP_005252328.1 |