Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGTTGCTAAAATGGTGAAATGCTG[C/G]TCCGCCATTGGATGTGCTTCTCGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607680 MIM: 612535 | ||||||||||||||||||||
Literature Links: |
RCHY1 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 |
RCHY1 - ring finger and CHY zinc finger domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009922.2 | 125 | Intron | NP_001009922.1 | |||
NM_001278536.1 | 125 | Intron | NP_001265465.1 | |||
NM_001278537.1 | 125 | Intron | NP_001265466.1 | |||
NM_001278538.1 | 125 | Intron | NP_001265467.1 | |||
NM_001278539.1 | 125 | Intron | NP_001265468.1 | |||
NM_015436.3 | 125 | Intron | NP_056251.2 | |||
XM_011531838.2 | 125 | Intron | XP_011530140.1 | |||
XM_011531839.2 | 125 | Intron | XP_011530141.1 |
THAP6 - THAP domain containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317791.1 | 125 | Missense Mutation | TGC,TGG | C,W 5 | NP_001304720.1 | |
NM_144721.5 | 125 | Missense Mutation | TGC,TGG | C,W 5 | NP_653322.1 | |
XM_005262772.2 | 125 | Intron | XP_005262829.1 | |||
XM_005262774.3 | 125 | Missense Mutation | TGC,TGG | C,W 5 | XP_005262831.1 | |
XM_006714109.3 | 125 | Missense Mutation | TGC,TGG | C,W 5 | XP_006714172.1 | |
XM_011531666.2 | 125 | Missense Mutation | TGC,TGG | C,W 5 | XP_011529968.1 | |
XM_011531667.2 | 125 | Missense Mutation | TGC,TGG | C,W 5 | XP_011529969.1 | |
XM_017007800.1 | 125 | Missense Mutation | TGC,TGG | C,W 5 | XP_016863289.1 | |
XM_017007801.1 | 125 | Missense Mutation | TGC,TGG | C,W 5 | XP_016863290.1 |