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GGAAATTTGTCCAATTGTTCATATG[C/T]CAGCCGCCCATCTTCTCCTAAATAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611410 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C6orf229 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C6orf229 - chromosome 6 open reading frame 229 | ||||||
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There are no transcripts associated with this gene. |
FAM65B - family with sequence similarity 65 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286445.1 | 3410 | Missense Mutation | ACA,GCA | T,A 1021 | NP_001273374.1 | |
NM_001286446.1 | 3410 | Intron | NP_001273375.1 | |||
NM_001286447.1 | 3410 | Intron | NP_001273376.1 | |||
NM_014722.3 | 3410 | Missense Mutation | ACA,GCA | T,A 1042 | NP_055537.2 | |
NM_015864.3 | 3410 | Intron | NP_056948.2 | |||
XM_006715275.2 | 3410 | Missense Mutation | ACA,GCA | T,A 1026 | XP_006715338.1 | |
XM_006715277.1 | 3410 | Missense Mutation | ACA,GCA | T,A 992 | XP_006715340.1 | |
XM_006715279.2 | 3410 | Missense Mutation | ACA,GCA | T,A 992 | XP_006715342.1 | |
XM_006715281.3 | 3410 | Intron | XP_006715344.1 | |||
XM_011515007.1 | 3410 | Missense Mutation | ACA,GCA | T,A 1021 | XP_011513309.1 | |
XM_011515008.2 | 3410 | Missense Mutation | ACA,GCA | T,A 992 | XP_011513310.1 | |
XM_011515009.1 | 3410 | Missense Mutation | ACA,GCA | T,A 992 | XP_011513311.1 | |
XM_011515010.2 | 3410 | Missense Mutation | ACA,GCA | T,A 992 | XP_011513312.1 | |
XM_011515012.1 | 3410 | Missense Mutation | ACA,GCA | T,A 1076 | XP_011513314.1 | |
XM_017011523.1 | 3410 | Missense Mutation | ACA,GCA | T,A 992 | XP_016867012.1 | |
XM_017011524.1 | 3410 | Intron | XP_016867013.1 | |||
XM_017011525.1 | 3410 | Intron | XP_016867014.1 | |||
XM_017011526.1 | 3410 | Intron | XP_016867015.1 | |||
XM_017011527.1 | 3410 | Intron | XP_016867016.1 |