Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTCCCGCAAATACTGCATCCATAC[A/G]GCTCCATTTCCAAATGAGGTCTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF248 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 |
ZNF248 - zinc finger protein 248 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267597.1 | 1031 | Missense Mutation | CCG,CTG | P,L 269 | NP_001254526.1 | |
NM_001267605.1 | 1031 | Intron | NP_001254534.1 | |||
NM_001267606.1 | 1031 | Intron | NP_001254535.1 | |||
NM_001267607.1 | 1031 | Intron | NP_001254536.1 | |||
NM_021045.2 | 1031 | Missense Mutation | CCG,CTG | P,L 269 | NP_066383.1 | |
XM_006717485.3 | 1031 | Missense Mutation | CCG,CTG | P,L 269 | XP_006717548.1 | |
XM_011519597.2 | 1031 | Missense Mutation | CCG,CTG | P,L 269 | XP_011517899.1 | |
XM_011519598.2 | 1031 | Intron | XP_011517900.1 | |||
XM_011519599.1 | 1031 | Intron | XP_011517901.1 | |||
XM_011519600.2 | 1031 | Intron | XP_011517902.1 | |||
XM_017016444.1 | 1031 | Missense Mutation | CCG,CTG | P,L 297 | XP_016871933.1 | |
XM_017016445.1 | 1031 | Missense Mutation | CCG,CTG | P,L 269 | XP_016871934.1 | |
XM_017016446.1 | 1031 | Missense Mutation | CCG,CTG | P,L 269 | XP_016871935.1 | |
XM_017016447.1 | 1031 | Intron | XP_016871936.1 | |||
XM_017016448.1 | 1031 | Intron | XP_016871937.1 | |||
XM_017016449.1 | 1031 | Intron | XP_016871938.1 | |||
XM_017016450.1 | 1031 | Intron | XP_016871939.1 | |||
XM_017016451.1 | 1031 | Intron | XP_016871940.1 |