Product Details

SNP ID

rs193142220

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:24591299 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGATCTATGTTTGGCACTGGCTGG[A/G]AGTCTACTGTGCTTTCCTCCTGCAC

Phenotype

MIM: 609870

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ARHGAP21 PubMed Links

Gene Details

Gene

ARHGAP21

Gene Name

Rho GTPase activating protein 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020824.3	4825	Intron			NP_065875.3
XM_005252542.3	4825	Intron			XP_005252599.1
XM_005252544.4	4825	Missense Mutation	TCC,TTC	S1349F	XP_005252601.1
XM_011519602.2	4825	Missense Mutation	TCC,TTC	S1393F	XP_011517904.1
XM_011519603.2	4825	Missense Mutation	TCC,TTC	S1393F	XP_011517905.1
XM_011519604.2	4825	Intron			XP_011517906.1
XM_011519605.2	4825	Missense Mutation	TCC,TTC	S1383F	XP_011517907.1
XM_011519606.2	4825	Missense Mutation	TCC,TTC	S1325F	XP_011517908.1
XM_011519607.2	4825	Intron			XP_011517909.1
XM_017016459.1	4825	Missense Mutation	TCC,TTC	S1359F	XP_016871948.1
XM_017016460.1	4825	Missense Mutation	TCC,TTC	S1349F	XP_016871949.1
XM_017016461.1	4825	Intron			XP_016871950.1

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