Colon Cancer: Gene >> CHSY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130185339:130185339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2197G>T
AA Mutation	p.Asp733Tyr(p.D733Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184999:130184999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857G>T
AA Mutation	p.Lys619Asn(p.K619N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130185237:130185237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2095C>T
AA Mutation	p.Leu699Phe(p.L699F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130185057:130185057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1915G>C
AA Mutation	p.Glu639Gln(p.E639Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184845:130184845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703G>A
AA Mutation	p.Ser568Asn(p.S568N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	129904863:129904863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34G>A
AA Mutation	p.Val12Met(p.V12M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184678:130184678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1536C>A
AA Mutation	p.Ser512Arg(p.S512R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184272:130184272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130G>T
AA Mutation	p.Gly377Val(p.G377V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184532:130184532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390A>T
AA Mutation	p.Ile464Leu(p.I464L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184536:130184536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394A>C
AA Mutation	p.Glu465Ala(p.E465A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130185027:130185027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145272862
CDS Mutation	c.1885G>A
AA Mutation	p.Gly629Arg(p.G629R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	130185716:130185716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148231534
CDS Mutation	c.2574C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	130184639:130184639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1497C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	129908318:129908318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373792516
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	129908186:129908186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHSY3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305031
Start	130184443:130184443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301T>A
AA Mutation	p.Leu434His(p.L434H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	130185641:130185641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2499C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	130185330:130185330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	129908111:129908111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305031
Start	130184948:130184948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1806G>A
Mutation Classification	Silent
Feature Type	Transcript