Colon Cancer: Gene >> ARHGAP24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85942069:85942069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395T>C
AA Mutation	p.Ile132Thr(p.I132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85977605:85977605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842A>G
AA Mutation	p.Asn281Ser(p.N281S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85994691:85994691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037A>T
AA Mutation	p.Asn346Ile(p.N346I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85721931:85721931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227A>T
AA Mutation	p.Asn76Ile(p.N76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	86000588:86000588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139260529
CDS Mutation	c.2113G>A
AA Mutation	p.Glu705Lys(p.E705K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85974951:85974951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796T>C
AA Mutation	p.Tyr266His(p.Y266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85994837:85994837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183C>A
AA Mutation	p.Leu395Ile(p.L395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85570595:85570595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>T
AA Mutation	p.Gln18His(p.Q18H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85995510:85995510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759004152
CDS Mutation	c.1856G>A
AA Mutation	p.Arg619Gln(p.R619Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000395184
Start	85995206:85995206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552G>T
AA Mutation	p.Glu518Ter(p.E518*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	86000521:86000521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046C>A
AA Mutation	p.Ser682Arg(p.S682R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395184
Start	85994940:85994940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>A
AA Mutation	p.Gly429Asp(p.G429D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395184
Start	85972114:85972114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779409795
CDS Mutation	c.678G>A
Mutation Classification	Silent
Feature Type	Transcript