Search Thermo Fisher Scientific
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CAACAGCTGCAAGCTAGATGAAGAC[A/G]ACACTGATAAATTAAAAGGCAAATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611212 | ||||||||||||||||||||
Literature Links: |
C4orf19 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 |
C4orf19 - chromosome 4 open reading frame 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001104629.1 | 356 | Missense Mutation | AAC,GAC | N,D 37 | NP_001098099.1 | |
NM_018302.2 | 356 | Missense Mutation | AAC,GAC | N,D 37 | NP_060772.2 | |
XM_011513712.2 | 356 | Missense Mutation | AAC,GAC | N,D 37 | XP_011512014.1 | |
XM_011513713.2 | 356 | Missense Mutation | AAC,GAC | N,D 37 | XP_011512015.1 | |
XM_017008361.1 | 356 | Missense Mutation | AAC,GAC | N,D 37 | XP_016863850.1 |
RELL1 - RELT like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085399.1 | 356 | Intron | NP_001078868.1 | |||
NM_001085400.1 | 356 | Intron | NP_001078869.1 | |||
XM_017008590.1 | 356 | Intron | XP_016864079.1 |