Product Details

SNP ID

rs145145100

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:61411920 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAATGGCTGTGAGCAGCGTCTCAA[C/T]TGCGTCACTGTAATCCCCTGATAAA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CPSF7 PubMed Links

Gene Details

Gene

CPSF7

Gene Name

cleavage and polyadenylation specific factor 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136040.2	1313	Missense Mutation	ATT,GTT	I368V	NP_001129512.1
NM_001142565.1	1313	Missense Mutation	ATT,GTT	I359V	NP_001136037.1
NM_024811.3	1313	Missense Mutation	ATT,GTT	I411V	NP_079087.3
XM_005274298.4	1313	Missense Mutation	ATT,GTT	I402V	XP_005274355.1
XM_005274299.4	1313	Missense Mutation	ATT,GTT	I368V	XP_005274356.1
XM_005274303.4	1313	Missense Mutation	ATT,GTT	I278V	XP_005274360.1
XM_011545257.2	1313	Missense Mutation	ATT,GTT	I344V	XP_011543559.1
XM_011545258.2	1313	Missense Mutation	ATT,GTT	I368V	XP_011543560.1
XM_011545259.2	1313	Missense Mutation	ATT,GTT	I359V	XP_011543561.1
XM_011545260.2	1313	Missense Mutation	ATT,GTT	I278V	XP_011543562.1
XM_011545261.2	1313	Missense Mutation	ATT,GTT	I278V	XP_011543563.1
XM_011545262.2	1313	Missense Mutation	ATT,GTT	I134V	XP_011543564.1
XM_011545263.2	1313	Missense Mutation	ATT,GTT	I134V	XP_011543565.1
XM_017018345.1	1313	Missense Mutation	ATT,GTT	I335V	XP_016873834.1

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