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SNP ID: rs201789727
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:74461488 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGGACCCTCCAGATGCCCATAGTG[A/G]TGGAGTGCTCCCAAAGCCAGGTAGT
Phenotype: MIM: 616456 MIM: 601336 MIM: 606961
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: INO80B PubMed Links

Gene Details

Gene: INO80B
Gene Name: INO80 complex subunit B

There are no transcripts associated with this gene.

Gene: INO80B-WBP1
Gene Name: INO80B-WBP1 readthrough (NMD candidate)

There are no transcripts associated with this gene.

Gene: MOGS
Gene Name: mannosyl-oligosaccharide glucosidase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146158.1	2227	Silent Mutation	CAC,CAT	H661H	NP_001139630.1
NM_006302.2	2227	Silent Mutation	CAC,CAT	H767H	NP_006293.2
XM_017004876.1	2227	Silent Mutation	CAC,CAT	H492H	XP_016860365.1
XM_017004877.1	2227	Silent Mutation	CAC,CAT	H492H	XP_016860366.1

Gene: WBP1
Gene Name: WW domain binding protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012477.3	2227	Intron			NP_036609.1

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