Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CIT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119735206:119735206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2984G>A
AA Mutation	p.Arg995His(p.R995H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119752133:119752133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2695G>A
AA Mutation	p.Ala899Thr(p.A899T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119758694:119758694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2302A>C
AA Mutation	p.Asn768His(p.N768H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119822826:119822826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754496604
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Cys(p.R369C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119857693:119857693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745580393
CDS Mutation	c.244G>A
AA Mutation	p.Asp82Asn(p.D82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261833
Start	119734356:119734356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3032C>T
AA Mutation	p.Thr1011Met(p.T1011M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119712615:119712615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4534G>A
AA Mutation	p.Glu1512Lys(p.E1512K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261833
Start	119850274:119850274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416T>G
AA Mutation	p.Val139Gly(p.V139G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119697988:119697988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763157071
CDS Mutation	c.5564G>A
AA Mutation	p.Arg1855His(p.R1855H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119752114:119752114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2714G>A
AA Mutation	p.Arg905His(p.R905H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119772864:119772864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1988G>A
AA Mutation	p.Arg663His(p.R663H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119714310:119714310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4067G>T
AA Mutation	p.Arg1356Leu(p.R1356L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119735246:119735246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2944G>A
AA Mutation	p.Asp982Asn(p.D982N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119713594:119713594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4235G>A
AA Mutation	p.Gly1412Asp(p.G1412D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119721343:119721343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3572G>T
AA Mutation	p.Arg1191Ile(p.R1191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119757480:119757480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2471G>A
AA Mutation	p.Gly824Glu(p.G824E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119850238:119850238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61735296
CDS Mutation	c.452G>A
AA Mutation	p.Arg151Gln(p.R151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119730581:119730581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3274G>A
AA Mutation	p.Ala1092Thr(p.A1092T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119775801:119775801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754514332
CDS Mutation	c.1926A>C
AA Mutation	p.Gln642His(p.Q642H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119782562:119782562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>T
AA Mutation	p.Asp541Tyr(p.D541Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119822913:119822913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018A>C
AA Mutation	p.Ser340Arg(p.S340R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119850253:119850253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757874504
CDS Mutation	c.437G>A
AA Mutation	p.Arg146Gln(p.R146Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119730599:119730599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3256C>T
AA Mutation	p.Arg1086Cys(p.R1086C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119776700:119776700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141341431
CDS Mutation	c.1808C>T
AA Mutation	p.Ala603Val(p.A603V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119735307:119735307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149750500
CDS Mutation	c.2883T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119825318:119825318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137928558
CDS Mutation	c.804G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119701944:119701944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5193A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119735325:119735325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2865G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119718405:119718405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3882C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119730621:119730621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138923592
CDS Mutation	c.3234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119697757:119697757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5658G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119784046:119784046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780631864
CDS Mutation	c.1407G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119697808:119697808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367573015
CDS Mutation	c.5607G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119730573:119730573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3282G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119734208:119734208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768920012
CDS Mutation	c.3180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000261833
Start	119735189:119735189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3001C>T
AA Mutation	p.Arg1001Ter(p.R1001*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000261833
Start	119734204:119734204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3184C>T
AA Mutation	p.Arg1062Ter(p.R1062*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CIT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119721441:119721441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3474A>C
AA Mutation	p.Lys1158Asn(p.K1158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119772883:119772883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778060632
CDS Mutation	c.1969G>A
AA Mutation	p.Glu657Lys(p.E657K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119735267:119735267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2923G>A
AA Mutation	p.Asp975Asn(p.D975N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119776772:119776772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736G>T
AA Mutation	p.Arg579Ile(p.R579I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119752059:119752059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2769G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119803280:119803280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000261833
Start	119713206:119713206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4450G>T
AA Mutation	p.Glu1484Ter(p.E1484*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript