Colon Cancer: Gene >> NFAT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69670023:69670023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1362C>A
AA Mutation	p.Ser454Arg(p.S454R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69692457:69692457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2578T>G
AA Mutation	p.Leu860Val(p.L860V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69692686:69692686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2807C>T
AA Mutation	p.Ser936Phe(p.S936F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69693683:69693683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3804T>G
AA Mutation	p.Ile1268Met(p.I1268M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69691892:69691892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2013C>G
AA Mutation	p.Asn671Lys(p.N671K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69693585:69693585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3706C>A
AA Mutation	p.His1236Asn(p.H1236N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69647529:69647529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701A>G
AA Mutation	p.His234Arg(p.H234R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354436
Start	69693953:69693953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4074T>G
AA Mutation	p.Ile1358Met(p.I1358M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354436
Start	69693371:69693371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762586717
CDS Mutation	c.3492G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354436
Start	69692993:69692993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3114C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000354436
Start	69659807:69659808(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1223_1224insTACAAAAGGGTAAATTCTAAACATT
AA Mutation	p.Arg410LysfsTer3(p.R410Kfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000354436
Start	69655800:69655800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NFAT5

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354436
Start	69693055:69693056(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3182dupT
AA Mutation	p.Leu1061PhefsTer35(p.L1061Ffs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript