Colon Cancer: Gene >> VSIG10L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51341215:51341215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760564636
CDS Mutation	c.833C>T
AA Mutation	p.Thr278Met(p.T278M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51341249:51341249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51341629:51341629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>T
AA Mutation	p.Thr140Ile(p.T140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51339050:51339050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567G>A
AA Mutation	p.Ala523Thr(p.A523T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51338908:51338908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1709G>A
AA Mutation	p.Arg570His(p.R570H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51338053:51338053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1885C>T
AA Mutation	p.Arg629Trp(p.R629W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51333870:51333870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2495G>A
AA Mutation	p.Ser832Asn(p.S832N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335624
Start	51337464:51337464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335624
Start	51341730:51341730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335624
Start	51334270:51334270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752884014
CDS Mutation	c.2340C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335624
Start	51337952:51337952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1986C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335624
Start	51341862:51341862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335624
Start	51341417:51341417(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.631delC
AA Mutation	p.Leu211Ter(p.L211*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335624
Start	51341261:51341261(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.787delG
AA Mutation	p.Val263PhefsTer72(p.V263Ffs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335624
Start	51338200:51338200(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1738delC
AA Mutation	p.Arg580GlufsTer108(p.R580Efs*108)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000335624
Start	51332639:51332640(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2575_2576insA
AA Mutation	p.Ala859AspfsTer24(p.A859Dfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> VSIG10L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51334199:51334199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746988635
CDS Mutation	c.2411G>A
AA Mutation	p.Arg804His(p.R804H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51337351:51337351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765141637
CDS Mutation	c.2192G>A
AA Mutation	p.Arg731Gln(p.R731Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335624
Start	51341281:51341281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767G>A
AA Mutation	p.Arg256Gln(p.R256Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335624
Start	51337978:51337978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1960C>T
Mutation Classification	Silent
Feature Type	Transcript