Product Details

SNP ID

rs1044414

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:21001138 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTGGTCACATGGGACCATTTCTGA[G/A]AATCTCGGCCCATCTCTGTTTCTCT

Phenotype

MIM: 612116

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

LOC105369205 PubMed Links

Gene Details

Gene

LOC105369205

Gene Name

uncharacterized LOC105369205

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011524128.2	3675	Intron			XP_011522430.1
XM_011524129.2	3675	Intron			XP_011522431.1
XM_011524131.2	3675	Intron			XP_011522433.1
XM_017025507.1	3675	Intron			XP_016880996.1
XM_017025508.1	3675	Intron			XP_016880997.1
XM_017025509.1	3675	Intron			XP_016880998.1

Gene

USP22

Gene Name

ubiquitin specific peptidase 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015276.1	3675	UTR 3			NP_056091.1
XM_005256575.2	3675	UTR 3			XP_005256632.1

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