Colon Cancer: Gene >> PIWIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24727977:24727977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2009T>G
AA Mutation	p.Val670Gly(p.V670G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24754122:24754122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748965457
CDS Mutation	c.869G>A
AA Mutation	p.Arg290Gln(p.R290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24755833:24755833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643A>T
AA Mutation	p.Thr215Ser(p.T215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24735714:24735714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1628C>T
AA Mutation	p.Ala543Val(p.A543V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24724929:24724929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780894038
CDS Mutation	c.2216C>T
AA Mutation	p.Ala739Val(p.A739V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24756622:24756622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779523659
CDS Mutation	c.439G>A
AA Mutation	p.Val147Ile(p.V147I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24754168:24754168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775556342
CDS Mutation	c.823G>A
AA Mutation	p.Glu275Lys(p.E275K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24754790:24754790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150240138
CDS Mutation	c.767G>A
AA Mutation	p.Arg256His(p.R256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24748933:24748933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761950809
CDS Mutation	c.1423G>A
AA Mutation	p.Ala475Thr(p.A475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24754077:24754077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914C>T
AA Mutation	p.Ala305Val(p.A305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24748925:24748925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201406937
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24748952:24748952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754382230
CDS Mutation	c.1404G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24728369:24728369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1740T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24725003:24725003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148843024
CDS Mutation	c.2142G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24728009:24728009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369368465
CDS Mutation	c.1977C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24725006:24725006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000332271
Start	24749480:24749480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>T
AA Mutation	p.Glu420Ter(p.E420*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000332271
Start	24719883:24719885(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2395_2397delTTT
AA Mutation	p.Phe799del(p.F799del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIWIL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24719768:24719768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2512C>T
AA Mutation	p.His838Tyr(p.H838Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24724999:24724999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2146C>T
AA Mutation	p.Pro716Ser(p.P716S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24754092:24754092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899G>A
AA Mutation	p.Arg300Lys(p.R300K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24728234:24728234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1875G>T
AA Mutation	p.Lys625Asn(p.K625N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332271
Start	24754830:24754830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142590557
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Cys(p.R243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24754187:24754187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24754129:24754129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773740105
CDS Mutation	c.862C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24719778:24719778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2502T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332271
Start	24755867:24755867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763366453
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript