Colon Cancer: Gene >> HIPK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113968603:113968603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370415621
CDS Mutation	c.2726G>A
AA Mutation	p.Arg909Gln(p.R909Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113941387:113941387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004T>C
AA Mutation	p.Val335Ala(p.V335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113940757:113940757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374G>A
AA Mutation	p.Arg125Gln(p.R125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113970132:113970132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374760868
CDS Mutation	c.2948G>A
AA Mutation	p.Arg983His(p.R983H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113968506:113968506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2629A>G
AA Mutation	p.Thr877Ala(p.T877A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113957161:113957161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762593832
CDS Mutation	c.1630C>T
AA Mutation	p.Arg544Trp(p.R544W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113968501:113968501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2624G>A
AA Mutation	p.Arg875His(p.R875H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113940415:113940415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32C>T
AA Mutation	p.Pro11Leu(p.P11L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113968585:113968585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2708T>C
AA Mutation	p.Val903Ala(p.V903A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113963486:113963486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2203C>T
AA Mutation	p.Arg735Trp(p.R735W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113957150:113957150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1619A>G
AA Mutation	p.Glu540Gly(p.E540G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113941323:113941323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940G>A
AA Mutation	p.Ala314Thr(p.A314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113954704:113954704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113963395:113963395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113970133:113970133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2949C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113973218:113973218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757463911
CDS Mutation	c.3339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113958227:113958227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113963446:113963446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2163G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113940500:113940500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369558
Start	113940473:113940473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000369558
Start	113973034:113973034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3155C>G
AA Mutation	p.Ser1052Ter(p.S1052*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369558
Start	113955620:113955621(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1383dupT
AA Mutation	p.Asn462Ter(p.N462*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HIPK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369558
Start	113970072:113970072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2888G>A
AA Mutation	p.Gly963Asp(p.G963D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000369558
Start	113941188:113941188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>T
AA Mutation	p.Glu269Ter(p.E269*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript