Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCGCTGCGGAGGCCTTCCAGCAG[C/T]GCCTACAGGACGAGCTGGGGGGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608592 | ||||||||||||||||||||
Literature Links: |
CTDSPL 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 |
CTDSPL - CTD small phosphatase like | ||||||
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There are no transcripts associated with this gene. |
VILL - villin like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015873.3 | 594 | Missense Mutation | CGC,TGC | R,C 82 | NP_056957.3 | |
XM_005265191.3 | 594 | Missense Mutation | CGC,TGC | R,C 82 | XP_005265248.1 | |
XM_005265192.4 | 594 | Missense Mutation | CGC,TGC | R,C 82 | XP_005265249.1 | |
XM_006713184.3 | 594 | Missense Mutation | CGC,TGC | R,C 82 | XP_006713247.1 | |
XM_011533770.2 | 594 | Missense Mutation | CGC,TGC | R,C 82 | XP_011532072.1 | |
XM_011533771.1 | 594 | Missense Mutation | CGC,TGC | R,C 82 | XP_011532073.1 | |
XM_011533773.2 | 594 | Missense Mutation | CGC,TGC | R,C 82 | XP_011532075.1 |