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TTTTCTCCATTTTAATGTTTTCCCA[C/T]GGCCAAAGCAGGGTGTCGGCTGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605211 MIM: 616533 | ||||||||||||||||||||
Literature Links: |
BARHL1 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 |
BARHL1 - BarH like homeobox 1 | ||||||
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There are no transcripts associated with this gene. |
DDX31 - DEAD-box helicase 31 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322340.1 | 2139 | Missense Mutation | NP_001309269.1 | |||
NM_001322341.1 | 2139 | Missense Mutation | NP_001309270.1 | |||
NM_001322342.1 | 2139 | Missense Mutation | NP_001309271.1 | |||
NM_001322343.1 | 2139 | Missense Mutation | NP_001309272.1 | |||
NM_001322344.1 | 2139 | Intron | NP_001309273.1 | |||
NM_022779.8 | 2139 | Missense Mutation | NP_073616.6 | |||
NM_138620.1 | 2139 | Intron | NP_619526.1 | |||
XM_005272207.4 | 2139 | Missense Mutation | XP_005272264.1 | |||
XM_006717236.3 | 2139 | UTR 3 | XP_006717299.1 | |||
XM_011518921.2 | 2139 | Intron | XP_011517223.1 | |||
XM_011518922.2 | 2139 | Intron | XP_011517224.1 |