Product Details

SNP ID
rs117586079
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:154739627 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTGTTACCTTTAGTTATATTTAG[A/G]ATACCTAAATTCTTAGTATTTTTTG
Phenotype
MIM: 616024
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SCAF8 PubMed Links

Gene Details

Gene
SCAF8
Gene Name
SR-related CTD associated factor 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286188.1 Intron NP_001273117.1
NM_001286189.1 Intron NP_001273118.1
NM_001286194.1 Intron NP_001273123.1
NM_001286199.1 Intron NP_001273128.1
NM_014892.4 Intron NP_055707.3

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