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GATGCTGTCTAACCTCCACGAGCTG[A/C]TTCCGAATCACCTGATGGAGACGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C6orf201 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 |
C6orf201 - chromosome 6 open reading frame 201 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085401.2 | 407 | Missense Mutation | ATT,CTT | I,L 9 | NP_001078870.1 | |
XM_005249112.3 | 407 | Missense Mutation | ATT,CTT | I,L 9 | XP_005249169.1 | |
XM_011514613.2 | 407 | Missense Mutation | ATT,CTT | I,L 9 | XP_011512915.1 | |
XM_017010861.1 | 407 | Intron | XP_016866350.1 |
FAM217A - family with sequence similarity 217 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173563.2 | 407 | Intron | NP_775834.2 | |||
XM_005248951.3 | 407 | Intron | XP_005249008.1 | |||
XM_006715025.2 | 407 | Intron | XP_006715088.1 | |||
XM_006715026.3 | 407 | Intron | XP_006715089.1 | |||
XM_011514413.2 | 407 | Intron | XP_011512715.1 | |||
XM_011514414.2 | 407 | Intron | XP_011512716.1 | |||
XM_011514415.1 | 407 | Intron | XP_011512717.1 | |||
XM_011514416.2 | 407 | Intron | XP_011512718.1 | |||
XM_011514417.1 | 407 | Intron | XP_011512719.1 | |||
XM_017010480.1 | 407 | Intron | XP_016865969.1 | |||
XM_017010481.1 | 407 | Intron | XP_016865970.1 | |||
XM_017010482.1 | 407 | Intron | XP_016865971.1 |