Colon Cancer: Gene >> NFATC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79451032:79451032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1668G>T
AA Mutation	p.Lys556Asn(p.K556N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79486652:79486652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2497A>G
AA Mutation	p.Ser833Gly(p.S833G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410445:79410445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779010195
CDS Mutation	c.170C>T
AA Mutation	p.Pro57Leu(p.P57L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79461333:79461333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1926G>A
AA Mutation	p.Met642Ile(p.M642I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79486932:79486932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2777A>G
AA Mutation	p.Asp926Gly(p.D926G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410501:79410501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226A>G
AA Mutation	p.Thr76Ala(p.T76A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79451003:79451003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639C>T
AA Mutation	p.Arg547Trp(p.R547W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410945:79410945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150129624
CDS Mutation	c.670G>A
AA Mutation	p.Gly224Arg(p.G224R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410567:79410567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375266848
CDS Mutation	c.292G>A
AA Mutation	p.Ala98Thr(p.A98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79461353:79461353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1946A>T
AA Mutation	p.Asp649Val(p.D649V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410695:79410695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420G>T
AA Mutation	p.Glu140Asp(p.E140D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79433683:79433683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331C>T
AA Mutation	p.Thr444Met(p.T444M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79467559:79467559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779877080
CDS Mutation	c.2069G>A
AA Mutation	p.Arg690His(p.R690H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79486824:79486824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2669C>A
AA Mutation	p.Ala890Asp(p.A890D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79411375:79411375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367652299
CDS Mutation	c.1100C>T
AA Mutation	p.Ala367Val(p.A367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410843:79410843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>A
AA Mutation	p.Glu190Lys(p.E190K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79451682:79451682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1769G>A
AA Mutation	p.Arg590His(p.R590H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410736:79410736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752605795
CDS Mutation	c.461C>T
AA Mutation	p.Thr154Met(p.T154M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79410795:79410795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520G>A
AA Mutation	p.Ala174Thr(p.A174T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79411116:79411116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841C>G
AA Mutation	p.His281Asp(p.H281D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427363
Start	79410863:79410863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536523701
CDS Mutation	c.588G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427363
Start	79411121:79411121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746768849
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427363
Start	79410866:79410866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748514998
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427363
Start	79410998:79410998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61731548
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NFATC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427363
Start	79451016:79451016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652C>T
AA Mutation	p.Thr551Met(p.T551M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript