Colon Cancer: Gene >> CCDC88C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91289308:91289308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4238A>T
AA Mutation	p.Lys1413Ile(p.K1413I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91281482:91281482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4674T>A
AA Mutation	p.Phe1558Leu(p.F1558L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91273521:91273521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5191C>T
AA Mutation	p.Pro1731Ser(p.P1731S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91408693:91408693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236C>T
AA Mutation	p.Thr79Ile(p.T79I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91291015:91291015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4182C>A
AA Mutation	p.Phe1394Leu(p.F1394L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91297474:91297474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3797A>G
AA Mutation	p.His1266Arg(p.H1266R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91313564:91313564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2252G>A
AA Mutation	p.Gly751Asp(p.G751D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91277987:91277987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4993C>T
AA Mutation	p.Pro1665Ser(p.P1665S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91297465:91297465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3806A>G
AA Mutation	p.Lys1269Arg(p.K1269R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91291062:91291062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4135A>G
AA Mutation	p.Arg1379Gly(p.R1379G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91313754:91313754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375082540
CDS Mutation	c.2062G>A
AA Mutation	p.Val688Met(p.V688M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91299943:91299943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3763C>T
AA Mutation	p.Arg1255Trp(p.R1255W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91313166:91313166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185802741
CDS Mutation	c.2650G>A
AA Mutation	p.Gly884Ser(p.G884S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91307207:91307207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3026C>T
AA Mutation	p.Thr1009Ile(p.T1009I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91273140:91273140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763090813
CDS Mutation	c.5572C>T
AA Mutation	p.Arg1858Trp(p.R1858W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91339297:91339297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376282183
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Trp(p.R264W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91273185:91273185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5527C>T
AA Mutation	p.His1843Tyr(p.H1843Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91313613:91313613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770066487
CDS Mutation	c.2203C>T
AA Mutation	p.Arg735Cys(p.R735C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91273134:91273134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200488874
CDS Mutation	c.5578C>T
AA Mutation	p.Arg1860Trp(p.R1860W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91339971:91339971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756135471
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91278102:91278102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4878C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91339316:91339316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557999756
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91278096:91278096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759681446
CDS Mutation	c.4884C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91339962:91339962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531052845
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91343611:91343611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91321264:91321264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753079228
CDS Mutation	c.1383G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91309942:91309942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2781G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91272652:91272652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367661539
CDS Mutation	c.6060C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91303949:91303949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770294143
CDS Mutation	c.3387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91313674:91313674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2142G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91303790:91303790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771345343
CDS Mutation	c.3546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91294304:91294304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201259963
CDS Mutation	c.3981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91313284:91313284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2532G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389857
Start	91291049:91291049(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4148delA
AA Mutation	p.Lys1383SerfsTer29(p.K1383Sfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC88C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389857
Start	91278110:91278110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4870G>A
AA Mutation	p.Gly1624Arg(p.G1624R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389857
Start	91273443:91273443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5269C>T
Mutation Classification	Silent
Feature Type	Transcript