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AGCTTTCGCACACCTCATGGGCCTT[C/T]GTGGGCTGCTGGAGAGATGTTGGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604760 | ||||||||||||||||||||
Literature Links: |
LOC100131655 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 |
LOC100131655 - uncharacterized LOC100131655 | ||||||
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There are no transcripts associated with this gene. |
ZNF236 - zinc finger protein 236 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306089.1 | 362 | Intron | NP_001293018.1 | |||
NM_007345.3 | 362 | Missense Mutation | CGT,TGT | R,C 4 | NP_031371.3 | |
XM_005266762.3 | 362 | Intron | XP_005266819.1 | |||
XM_011526165.2 | 362 | Missense Mutation | CGT,TGT | R,C 4 | XP_011524467.1 | |
XM_011526166.2 | 362 | Intron | XP_011524468.1 | |||
XM_011526168.2 | 362 | Intron | XP_011524470.1 | |||
XM_011526169.2 | 362 | Intron | XP_011524471.1 |