Product Details

SNP ID

rs3135550

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:33820146 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTCACCCACTCATCTTTATAGCCTT[C/T]ATAGCACTGGTTCCCAAACCAGACT

Phenotype

MIM: 600405

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RFC3 PubMed Links

Gene Details

Gene

RFC3

Gene Name

replication factor C subunit 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002915.3		Intron			NP_002906.1
NM_181558.2		Intron			NP_853536.2
XM_011535172.2		Intron			XP_011533474.1
XM_011535173.2		Intron			XP_011533475.1
XM_011535174.2		Intron			XP_011533476.1
XM_011535175.1		Intron			XP_011533477.1
XM_017020680.1		Intron			XP_016876169.1
XM_017020681.1		Intron			XP_016876170.1
XM_017020682.1		Intron			XP_016876171.1
XM_017020683.1		Intron			XP_016876172.1

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