Colon Cancer: Gene >> NFATC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68191530:68191530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2861C>A
AA Mutation	p.Ser954Tyr(p.S954Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68191104:68191104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200413040
CDS Mutation	c.2435A>G
AA Mutation	p.Asn812Ser(p.N812S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68181481:68181481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772345934
CDS Mutation	c.1922G>A
AA Mutation	p.Arg641Gln(p.R641Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346183
Start	68126608:68126608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1399A>G
AA Mutation	p.Lys467Glu(p.K467E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68191402:68191402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2733A>T
AA Mutation	p.Gln911His(p.Q911H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68191710:68191710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3041C>A
AA Mutation	p.Pro1014His(p.P1014H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68122218:68122218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335A>G
AA Mutation	p.Gln112Arg(p.Q112R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68191761:68191761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3092T>C
AA Mutation	p.Ile1031Thr(p.I1031T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68122488:68122488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565797863
CDS Mutation	c.605G>A
AA Mutation	p.Arg202Gln(p.R202Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68157884:68157884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1417G>A
AA Mutation	p.Glu473Lys(p.E473K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68191496:68191496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2827C>T
AA Mutation	p.Pro943Ser(p.P943S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346183
Start	68190868:68190868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2199A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346183
Start	68122532:68122532(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.653delG
AA Mutation	p.Gly218AlafsTer38(p.G218Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346183
Start	68085763:68085763(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.86delC
AA Mutation	p.Pro29ArgfsTer21(p.P29Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000346183
Start	68166892:68166892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651C>T
AA Mutation	p.Arg551Ter(p.R551*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346183
Start	68174493:68174494(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1899dupT
AA Mutation	p.Leu634SerfsTer2(p.L634Sfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NFATC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346183
Start	68183348:68183348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751577319
CDS Mutation	c.2080C>T
AA Mutation	p.Arg694Cys(p.R694C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346183
Start	68122304:68122304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346183
Start	68191213:68191213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2544A>C
Mutation Classification	Silent
Feature Type	Transcript