Product Details

SNP ID

rs140982927

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:76154472 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGCTGAGCCCCCGACAGCAGAGG[C/T]GGCAGCTTCGGAAACGCCGAGGTCG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

GPATCH2L PubMed Links

Gene Details

Gene

GPATCH2L

Gene Name

G-patch domain containing 2 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322026.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308955.1
NM_001322027.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308956.1
NM_001322028.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308957.1
NM_001322029.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308958.1
NM_001322030.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308959.1
NM_001322031.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308960.1
NM_001322032.1	426	Missense Mutation	CGG,TGG	R37W	NP_001308961.1
NM_017926.3	426	Missense Mutation	CGG,TGG	R37W	NP_060396.2
NM_017972.3	426	Missense Mutation	CGG,TGG	R37W	NP_060442.2
XM_006720191.2	426	Missense Mutation	CGG,TGG	R37W	XP_006720254.1
XM_017021427.1	426	Missense Mutation	CGG,TGG	R50W	XP_016876916.1
XM_017021428.1	426	Missense Mutation	CGG,TGG	R50W	XP_016876917.1
XM_017021429.1	426	Missense Mutation	CGG,TGG	R50W	XP_016876918.1
XM_017021430.1	426	Missense Mutation	CGG,TGG	R50W	XP_016876919.1
XM_017021431.1	426	Missense Mutation	CGG,TGG	R50W	XP_016876920.1
XM_017021432.1	426	Missense Mutation	CGG,TGG	R50W	XP_016876921.1
XM_017021433.1	426	Missense Mutation	CGG,TGG	R37W	XP_016876922.1

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