Colon Cancer: Gene >> NFATC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24376671:24376671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779918597
CDS Mutation	c.2434C>T
AA Mutation	p.Arg812Trp(p.R812W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24369778:24369778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>T
AA Mutation	p.Pro127Leu(p.P127L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24376068:24376068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2023C>T
AA Mutation	p.Arg675Cys(p.R675C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24369622:24369622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224C>T
AA Mutation	p.Pro75Leu(p.P75L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24376873:24376873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2636A>C
AA Mutation	p.Glu879Ala(p.E879A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24370020:24370020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24373706:24373706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778408359
CDS Mutation	c.1571C>T
AA Mutation	p.Ala524Val(p.A524V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24370204:24370204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806G>A
AA Mutation	p.Arg269Gln(p.R269Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24372595:24372595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138954014
CDS Mutation	c.1351G>A
AA Mutation	p.Val451Ile(p.V451I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24370389:24370389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.991C>T
AA Mutation	p.Arg331Trp(p.R331W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24376620:24376620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2383C>T
AA Mutation	p.Arg795Trp(p.R795W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24369673:24369673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766927800
CDS Mutation	c.275C>T
AA Mutation	p.Ser92Leu(p.S92L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24377677:24377677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2681C>T
AA Mutation	p.Ala894Val(p.A894V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24374394:24374394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1801G>T
AA Mutation	p.Gly601Cys(p.G601C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24369617:24369617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24375664:24375664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1878G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24372585:24372585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564143493
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24373704:24373704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552610225
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24370053:24370053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24376673:24376673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2436G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24372472:24372472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377116679
CDS Mutation	c.1228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250373
Start	24368408:24368408(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.74delC
AA Mutation	p.Pro25ArgfsTer69(p.P25Rfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250373
Start	24376395:24376395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2163delC
AA Mutation	p.Tyr722ThrfsTer122(p.Y722Tfs*122)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250373
Start	24376662:24376663(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2430dupC
AA Mutation	p.Phe811LeufsTer13(p.F811Lfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250373
Start	24376789:24376790(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2557dupG
AA Mutation	p.Ala853GlyfsTer31(p.A853Gfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NFATC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24369616:24369616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>T
AA Mutation	p.Ser73Leu(p.S73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250373
Start	24369769:24369769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>T
AA Mutation	p.Thr124Met(p.T124M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250373
Start	24376433:24376433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141569636
CDS Mutation	c.2196C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250373
Start	24376395:24376395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2163delC
AA Mutation	p.Tyr722ThrfsTer122(p.Y722Tfs*122)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript