Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTGTGTGGCCTTATCCGCGCATG[T/A]GCGGAGGCCCTGCGCAGCCTGCAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616128 MIM: 606044 | ||||||||||||||||||||
Literature Links: |
EHBP1L1 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 |
EHBP1L1 - EH domain binding protein 1 like 1 | ||||||
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There are no transcripts associated with this gene. |
FAM89B - family with sequence similarity 89 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098784.1 | 687 | Intron | NP_001092254.1 | |||
NM_001098785.1 | 687 | Intron | NP_001092255.1 | |||
NM_152832.2 | 687 | Intron | NP_690045.1 |
SSSCA1 - Sjogren syndrome/scleroderma autoantigen 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303024.1 | 687 | Nonsense Mutation | TGA,TGT | *,C 150 | NP_001289953.1 | |
NM_006396.2 | 687 | Nonsense Mutation | TGA,TGT | *,C 187 | NP_006387.1 |
SSSCA1-AS1 - SSSCA1 antisense RNA 1 (head to head) | ||||||
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There are no transcripts associated with this gene. |