Product Details

SNP ID

rs1728647

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:105539040 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGATTGTCAGGCTTCAGAAAGTAA[C/G]CTTTGTTATCTATCTCTACTTTTTG

Phenotype

MIM: 610089

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RINT1 PubMed Links

Gene Details

Gene

RINT1

Gene Name

RAD50 interactor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021930.4		Intron			NP_068749.3
XM_005250524.3		Intron			XP_005250581.1
XM_011516458.2		Intron			XP_011514760.1
XM_017012496.1		Intron			XP_016867985.1
XM_017012497.1		Intron			XP_016867986.1
XM_017012498.1		Intron			XP_016867987.1

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