Product Details

SNP ID

rs199667306

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:113799371 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGACGATGATTTCTGCAGAAGGAT[C/T]TAGAAGTCTGGGTAGAAACTCCCCT

Phenotype

MIM: 610748

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC390251 PubMed Links

Gene Details

Gene

LOC390251

Gene Name

SH3 domain containing GRB2 like 1 pseudogene

There are no transcripts associated with this gene.

Gene

USP28

Gene Name

ubiquitin specific peptidase 28

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301029.1	3357	Missense Mutation	AAT,GAT	N878D	NP_001287958.1
NM_020886.3	3357	Missense Mutation	AAT,GAT	N1035D	NP_065937.1
XM_005271630.2	3357	Missense Mutation	AAT,GAT	N1098D	XP_005271687.1
XM_005271631.2	3357	Missense Mutation	AAT,GAT	N1097D	XP_005271688.1
XM_005271632.2	3357	Missense Mutation	AAT,GAT	N1095D	XP_005271689.1
XM_005271633.4	3357	Missense Mutation	AAT,GAT	N1076D	XP_005271690.1
XM_005271636.2	3357	Missense Mutation	AAT,GAT	N1038D	XP_005271693.1
XM_005271637.2	3357	Missense Mutation	AAT,GAT	N1036D	XP_005271694.1
XM_005271638.2	3357	Missense Mutation	AAT,GAT	N1004D	XP_005271695.1
XM_005271639.2	3357	Missense Mutation	AAT,GAT	N1003D	XP_005271696.1
XM_011542936.2	3357	Missense Mutation	AAT,GAT	N1072D	XP_011541238.1
XM_011542938.1	3357	Missense Mutation	AAT,GAT	N973D	XP_011541240.1
XM_011542941.1	3357	Missense Mutation	AAT,GAT	N745D	XP_011541243.1
XM_011542942.1	3357	Missense Mutation	AAT,GAT	N654D	XP_011541244.1
XM_017018056.1	3357	Missense Mutation	AAT,GAT	N1071D	XP_016873545.1
XM_017018057.1	3357	Missense Mutation	AAT,GAT	N1032D	XP_016873546.1
XM_017018058.1	3357	Missense Mutation	AAT,GAT	N1009D	XP_016873547.1
XM_017018059.1	3357	Missense Mutation	AAT,GAT	N977D	XP_016873548.1
XM_017018060.1	3357	Missense Mutation	AAT,GAT	N972D	XP_016873549.1
XM_017018061.1	3357	Missense Mutation	AAT,GAT	N911D	XP_016873550.1
XM_017018062.1	3357	Missense Mutation	AAT,GAT	N910D	XP_016873551.1
XM_017018063.1	3357	Missense Mutation	AAT,GAT	N810D	XP_016873552.1
XM_017018064.1	3357	Missense Mutation	AAT,GAT	N748D	XP_016873553.1
XM_017018065.1	3357	Missense Mutation	AAT,GAT	N683D	XP_016873554.1
XM_017018066.1	3357	Missense Mutation	AAT,GAT	N683D	XP_016873555.1
XM_017018067.1	3357	Missense Mutation	AAT,GAT	N683D	XP_016873556.1
XM_017018068.1	3357	Missense Mutation	AAT,GAT	N651D	XP_016873557.1
XM_017018069.1	3357	Intron			XP_016873558.1

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