Product Details

SNP ID
rs144020235
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:45396221 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGGGCCTCACCGTGGTCCACCTTA[C/T]AGCGTAGCTTCTGGATGGTGGCCAG
Phenotype
MIM: 610591
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ARHGAP27 PubMed Links

Gene Details

Gene
ARHGAP27
Gene Name
Rho GTPase activating protein 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282290.1 2637 Missense Mutation NP_001269219.1
NM_174919.3 2637 Intron NP_777579.2
NM_199282.2 2637 Missense Mutation NP_954976.1
XM_005257128.3 2637 Missense Mutation XP_005257185.1
XM_006721745.2 2637 Missense Mutation XP_006721808.1
XM_006721747.2 2637 Missense Mutation XP_006721810.1
XM_006721750.3 2637 Intron XP_006721813.1
XM_011524468.1 2637 Missense Mutation XP_011522770.1
XM_011524469.1 2637 Missense Mutation XP_011522771.1
XM_011524470.2 2637 Missense Mutation XP_011522772.1
XM_011524471.1 2637 Missense Mutation XP_011522773.1
XM_011524472.2 2637 Missense Mutation XP_011522774.1
XM_011524473.2 2637 Intron XP_011522775.1
XM_011524474.1 2637 Missense Mutation XP_011522776.1
XM_017024311.1 2637 Missense Mutation XP_016879800.1
XM_017024312.1 2637 Missense Mutation XP_016879801.1
XM_017024313.1 2637 Intron XP_016879802.1

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