Colon Cancer: Gene >> CD22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35345668:35345668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2275G>A
AA Mutation	p.Gly759Ser(p.G759S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35332736:35332736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>T
AA Mutation	p.Arg75Ile(p.R75I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35345108:35345108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2190C>A
AA Mutation	p.Phe730Leu(p.F730L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35346188:35346188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2365G>T
AA Mutation	p.Asp789Tyr(p.D789Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35341788:35341788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369740146
CDS Mutation	c.1858G>A
AA Mutation	p.Ala620Thr(p.A620T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35346644:35346644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547905156
CDS Mutation	c.2491G>A
AA Mutation	p.Gly831Arg(p.G831R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35341070:35341070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439C>T
AA Mutation	p.Thr480Ile(p.T480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35344922:35344922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776104112
CDS Mutation	c.2129G>A
AA Mutation	p.Arg710Gln(p.R710Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000085219
Start	35341704:35341704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1774G>A
AA Mutation	p.Ala592Thr(p.A592T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35332837:35332837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325G>A
AA Mutation	p.Val109Met(p.V109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35341933:35341933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2003G>A
AA Mutation	p.Gly668Asp(p.G668D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35346577:35346577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2424G>T
AA Mutation	p.Glu808Asp(p.E808D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35346198:35346198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2375A>G
AA Mutation	p.Asp792Gly(p.D792G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35345068:35345068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150G>A
AA Mutation	p.Ser717Asn(p.S717N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35341891:35341891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771134417
CDS Mutation	c.1961C>T
AA Mutation	p.Ser654Leu(p.S654L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35341053:35341053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199643177
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35341023:35341023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35346202:35346202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371559984
CDS Mutation	c.2379G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35337996:35337996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550216523
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35332578:35332578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.66T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35344869:35344869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749416520
CDS Mutation	c.2076C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35336109:35336109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35337762:35337762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.726G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35336241:35336241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000085219
Start	35345612:35345612(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2224delC
AA Mutation	p.Leu742SerfsTer14(p.L742Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000085219
Start	35345118:35345201(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2200_2208+75delAATAAAAAGGTAGGATGGGGCTGGGCACGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CD22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35344888:35344888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2095C>A
AA Mutation	p.Leu699Ile(p.L699I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35332606:35332606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>A
AA Mutation	p.Leu32Ile(p.L32I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35340940:35340940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1309A>C
AA Mutation	p.Thr437Pro(p.T437P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000085219
Start	35346684:35346684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2531T>C
AA Mutation	p.Ile844Thr(p.I844T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35332740:35332740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139372163
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35337996:35337996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550216523
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000085219
Start	35336136:35336136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534159105
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000085219
Start	35337957:35337957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921C>A
AA Mutation	p.Tyr307Ter(p.Y307*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000085219
Start	35338296:35338296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114G>T
AA Mutation	p.Glu372Ter(p.E372*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript