Product Details

SNP ID

rs146593098

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:54171993 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACTCCTCATCACCTCTGCTGCCA[T/-]CTCCCTGGTCCTGGCCCTCATCCCC

Phenotype

MIM: 607753

Polymorphism

T/-, Insertion/deletion

Allele Nomenclature

Literature Links

SMUG1 PubMed Links

Gene Details

Gene

SMUG1

Gene Name

single-strand-selective monofunctional uracil-DNA glycosylase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243787.1	942	Intron			NP_001230716.1
NM_001243788.1	942	Intron			NP_001230717.1
NM_001243789.1	942	Intron			NP_001230718.1
NM_001243790.1	942	Intron			NP_001230719.1
NM_001243791.1	942	Intron			NP_001230720.1
NM_014311.2	942	Intron			NP_055126.1
XM_006719319.3	942	Intron			XP_006719382.1
XM_006719320.3	942	Intron			XP_006719383.1
XM_006719321.3	942	Intron			XP_006719384.1
XM_006719322.3	942	Intron			XP_006719385.1
XM_011538109.2	942	Intron			XP_011536411.1
XM_011538110.2	942	Intron			XP_011536412.1
XM_011538111.2	942	Intron			XP_011536413.1
XM_011538112.2	942	Intron			XP_011536414.1
XM_011538113.2	942	Intron			XP_011536415.1
XM_011538114.2	942	Intron			XP_011536416.1
XM_011538115.2	942	Intron			XP_011536417.1
XM_011538116.2	942	Intron			XP_011536418.1
XM_011538117.2	942	Intron			XP_011536419.1
XM_011538118.2	942	Intron			XP_011536420.1
XM_011538119.2	942	Intron			XP_011536421.1
XM_011538120.2	942	Intron			XP_011536422.1
XM_011538121.2	942	Intron			XP_011536423.1
XM_011538122.2	942	Intron			XP_011536424.1
XM_011538123.2	942	UTR 3			XP_011536425.1
XM_017019113.1	942	Intron			XP_016874602.1
XM_017019114.1	942	Intron			XP_016874603.1
XM_017019115.1	942	Intron			XP_016874604.1
XM_017019116.1	942	Intron			XP_016874605.1
XM_017019117.1	942	Intron			XP_016874606.1
XM_017019118.1	942	Intron			XP_016874607.1
XM_017019119.1	942	Intron			XP_016874608.1
XM_017019120.1	942	Intron			XP_016874609.1

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