Product Details

SNP ID
rs57492770
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:70304999 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTTCATGTGAGGCGTGTTTTATC[C/T]ATATATTTCAGTGTCTACTTTTTTG
Phenotype
MIM: 605812
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
DDX19B PubMed Links

Gene Details

Gene
DDX19B
Gene Name
DEAD-box helicase 19B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001014449.2 Intron NP_001014449.1
NM_001014451.2 Intron NP_001014451.1
NM_001257172.1 Intron NP_001244101.1
NM_001257173.1 Intron NP_001244102.1
NM_001257174.1 Intron NP_001244103.1
NM_001257175.1 Intron NP_001244104.1
NM_007242.5 Intron NP_009173.1
XM_006721127.2 Intron XP_006721190.1
XM_011522832.2 Intron XP_011521134.1
XM_011522833.2 Intron XP_011521135.1
XM_011522834.2 Intron XP_011521136.1
XM_017022890.1 Intron XP_016878379.1

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