Product Details

SNP ID: rs145867502
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:10984227 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCGGGCCCTGGCCCTTCCCCTGGA[A/G]CCATGCTGGGCCCTAGCCCGGGTCC
Phenotype: MIM: 603254
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SMARCA4 PubMed Links

Gene Details

Gene: SMARCA4
Gene Name: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128844.1	357	Missense Mutation	ACC,GCC	T26A	NP_001122316.1
NM_001128845.1	357	Missense Mutation	ACC,GCC	T26A	NP_001122317.1
NM_001128846.1	357	Missense Mutation	ACC,GCC	T26A	NP_001122318.1
NM_001128847.1	357	Missense Mutation	ACC,GCC	T26A	NP_001122319.1
NM_001128848.1	357	Missense Mutation	ACC,GCC	T26A	NP_001122320.1
NM_001128849.1	357	Missense Mutation	ACC,GCC	T26A	NP_001122321.1
NM_003072.3	357	Missense Mutation	ACC,GCC	T26A	NP_003063.2
XM_006722845.2	357	Missense Mutation	ACC,GCC	T26A	XP_006722908.1
XM_006722846.2	357	Missense Mutation	ACC,GCC	T26A	XP_006722909.1
XM_011528198.1	357	Missense Mutation	ACC,GCC	T26A	XP_011526500.1
XM_017027160.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882649.1
XM_017027161.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882650.1
XM_017027162.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882651.1
XM_017027163.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882652.1
XM_017027164.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882653.1
XM_017027165.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882654.1
XM_017027166.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882655.1
XM_017027167.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882656.1
XM_017027168.1	357	Missense Mutation	ACC,GCC	T26A	XP_016882657.1