Colon Cancer: Gene >> FRMD4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13656819:13656819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2770G>A
AA Mutation	p.Val924Ile(p.V924I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13701383:13701383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932C>T
AA Mutation	p.Ala311Val(p.A311V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13693997:13693997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018G>A
AA Mutation	p.Asp340Asn(p.D340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13761657:13761657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>T
AA Mutation	p.Asp152Tyr(p.D152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13656727:13656727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2862C>G
AA Mutation	p.Asp954Glu(p.D954E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13782937:13782937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369G>C
AA Mutation	p.Lys123Asn(p.K123N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357447
Start	13675042:13675042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120T>C
AA Mutation	p.Ser374Pro(p.S374P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13660338:13660338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747029408
CDS Mutation	c.1876C>T
AA Mutation	p.Arg626Cys(p.R626C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13666208:13666208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1492A>C
AA Mutation	p.Thr498Pro(p.T498P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13657383:13657383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206C>T
AA Mutation	p.Arg736Cys(p.R736C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13657388:13657388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2201G>A
AA Mutation	p.Arg734Gln(p.R734Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13670521:13670521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259C>T
AA Mutation	p.Thr420Met(p.T420M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13666258:13666258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754642787
CDS Mutation	c.1442G>A
AA Mutation	p.Arg481His(p.R481H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357447
Start	13782923:13782923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383A>G
AA Mutation	p.Lys128Arg(p.K128R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13693926:13693926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751351710
CDS Mutation	c.1089C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13656751:13656751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2838G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13656807:13656807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2782C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13656982:13656982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2607G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13659409:13659409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368935593
CDS Mutation	c.1980C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13674986:13674986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13740541:13740541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780552624
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13656865:13656865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357447
Start	13670483:13670483(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1297delG
AA Mutation	p.Glu433ArgfsTer10(p.E433Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357447
Start	13654452:13654452(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3014delC
AA Mutation	p.Pro1005GlnfsTer8(p.P1005Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000357447
Start	13659441:13659441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1948G>T
AA Mutation	p.Gly650Ter(p.G650*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000357447
Start	13707074:13707074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>T
AA Mutation	p.Glu267Ter(p.E267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357447
Start	13654451:13654452(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs752538869
CDS Mutation	c.3014dupC
AA Mutation	p.Ser1006LysfsTer25(p.S1006Kfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FRMD4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13666180:13666180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1520T>A
AA Mutation	p.Leu507Gln(p.L507Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13660491:13660491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376696301
CDS Mutation	c.1723C>T
AA Mutation	p.Arg575Trp(p.R575W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357447
Start	13740232:13740232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634T>A
AA Mutation	p.Ser212Thr(p.S212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13656784:13656784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2805C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13666179:13666179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1521G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13701445:13701445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188864146
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357447
Start	13701427:13701427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779028865
CDS Mutation	c.888G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000357447
Start	13762659:13762659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406G>T
AA Mutation	p.Glu136Ter(p.E136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript