Product Details

SNP ID
rs148616899
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:44977418 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAGTTCATGGATCACCGGGAGGT[C/G]CGAGTAGAGTGTTCTGAGGACACTG
Phenotype
MIM: 611309 MIM: 610559
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C10orf10 PubMed Links

Gene Details

Gene
C10orf10
Gene Name
chromosome 10 open reading frame 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007021.3 903 Missense Mutation CAC,GAC H205D NP_008952.1
Gene
RASSF4
Gene Name
Ras association domain family member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032023.3 903 Intron NP_114412.2
XM_005271833.4 903 Intron XP_005271890.1
XM_005271835.4 903 Intron XP_005271892.1
XM_006718013.3 903 Intron XP_006718076.1
XM_006718014.3 903 Intron XP_006718077.1
XM_011540255.2 903 Intron XP_011538557.1
XM_017016754.1 903 Intron XP_016872243.1
XM_017016755.1 903 Intron XP_016872244.1
XM_017016756.1 903 Intron XP_016872245.1
XM_017016757.1 903 Intron XP_016872246.1
XM_017016758.1 903 Intron XP_016872247.1

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