Product Details

SNP ID

rs3735165

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:150371282 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCAGGGGCCCCCTGGCCATGGGCC[T/C]GGCCCAGCCCCGACTCCTTTCTGGG

Phenotype

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

REPIN1 PubMed Links

Gene Details

Gene

REPIN1

Gene Name

replication initiator 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099695.1	114	Missense Mutation	CCG,CTG	P71L	NP_001093165.1
NM_001099696.2	114	Missense Mutation	CCG,CTG	P14L	NP_001093166.1
NM_013400.3	114	Missense Mutation	CCG,CTG	P14L	NP_037532.2
NM_014374.3	114	Missense Mutation	CCG,CTG	P14L	NP_055189.2
XM_005249985.1	114	Missense Mutation	CCG,CTG	P14L	XP_005250042.1
XM_006715947.3	114	Missense Mutation	CCG,CTG	P71L	XP_006716010.1
XM_006715948.3	114	Missense Mutation	CCG,CTG	P71L	XP_006716011.1
XM_006715949.3	114	Missense Mutation	CCG,CTG	P71L	XP_006716012.1
XM_006715950.3	114	Missense Mutation	CCG,CTG	P70L	XP_006716013.1
XM_006715951.2	114	Missense Mutation	CCG,CTG	P70L	XP_006716014.1
XM_006715952.2	114	Missense Mutation	CCG,CTG	P14L	XP_006716015.1
XM_006715953.2	114	Missense Mutation	CCG,CTG	P14L	XP_006716016.1
XM_011516112.1	114	Missense Mutation	CCG,CTG	P14L	XP_011514414.1
XM_017012081.1	114	Missense Mutation	CCG,CTG	P14L	XP_016867570.1
XM_017012082.1	114	Missense Mutation	CCG,CTG	P14L	XP_016867571.1

Gene

ZNF775

Gene Name

zinc finger protein 775

There are no transcripts associated with this gene.

View Full Product Details