Product Details

SNP ID
rs201385244
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:176529568 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGTCCGGGTTAAAGCGGTACGAC[A/G]GGAGCTGCTCTATGTCTGCTTTGGT
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RNF44 PubMed Links

Gene Details

Gene
RNF44
Gene Name
ring finger protein 44
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014901.4 1507 Missense Mutation CCG,CTG P364L NP_055716.1
XM_005265840.2 1507 Missense Mutation CCG,CTG P364L XP_005265897.1
XM_005265841.4 1507 Missense Mutation CCG,CTG P364L XP_005265898.1
XM_005265842.4 1507 Missense Mutation CCG,CTG P283L XP_005265899.1
XM_005265843.2 1507 Missense Mutation CCG,CTG P283L XP_005265900.1
XM_005265844.3 1507 Missense Mutation CCG,CTG P283L XP_005265901.1
XM_005265845.4 1507 Missense Mutation CCG,CTG P283L XP_005265902.1
XM_006714831.2 1507 Missense Mutation CCG,CTG P361L XP_006714894.1
XM_006714832.2 1507 Missense Mutation CCG,CTG P317L XP_006714895.1
XM_011534466.2 1507 Missense Mutation CCG,CTG P364L XP_011532768.1
XM_011534467.2 1507 Missense Mutation CCG,CTG P283L XP_011532769.1

View Full Product Details