Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGGTAAAGGGCGCGGGTGCCCTCT[C/T]GCTGCAAGATCTGCCTGGCGCAGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603445 MIM: 608746 MIM: 610822 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KHSRP PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KHSRP - KH-type splicing regulatory protein | ||||||
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There are no transcripts associated with this gene. |
SLC25A23 - solute carrier family 25 member 23 | ||||||
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There are no transcripts associated with this gene. |
SLC25A41 - solute carrier family 25 member 41 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321298.1 | 584 | Missense Mutation | NP_001308227.1 | |||
NM_173637.3 | 584 | Missense Mutation | NP_775908.2 | |||
XM_011527926.1 | 584 | Missense Mutation | XP_011526228.1 |