Colon Cancer: Gene >> PIWIL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22279463:22279463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77G>A
AA Mutation	p.Gly26Asp(p.G26D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22355485:22355485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768769441
CDS Mutation	c.2902G>A
AA Mutation	p.Glu968Lys(p.E968K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22289915:22289915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055T>G
AA Mutation	p.Leu352Arg(p.L352R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22311142:22311142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831C>A
AA Mutation	p.Pro611Thr(p.P611T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22311152:22311152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761129029
CDS Mutation	c.1841C>T
AA Mutation	p.Ala614Val(p.A614V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22279448:22279448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62C>A
AA Mutation	p.Ala21Asp(p.A21D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22353093:22353093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2538G>T
AA Mutation	p.Lys846Asn(p.K846N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22283060:22283060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181413985
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22304113:22304113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749111384
CDS Mutation	c.1274G>A
AA Mutation	p.Arg425His(p.R425H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22316324:22316324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2288G>A
AA Mutation	p.Ser763Asn(p.S763N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22316316:22316316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746837231
CDS Mutation	c.2280C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22354334:22354334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2721C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22316322:22316322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2286A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356766
Start	22304856:22304856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000356766
Start	22305926:22305926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PIWIL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22315085:22315085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2148G>T
AA Mutation	p.Lys716Asn(p.K716N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22281201:22281201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765790303
CDS Mutation	c.280C>T
AA Mutation	p.Pro94Ser(p.P94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22304195:22304195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1356C>A
AA Mutation	p.Phe452Leu(p.F452L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356766
Start	22287638:22287638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854T>C
AA Mutation	p.Leu285Pro(p.L285P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000356766
Start	22310010:22310010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1736C>A
AA Mutation	p.Ser579Ter(p.S579*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000356766
Start	22284163:22284163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634G>T
AA Mutation	p.Glu212Ter(p.E212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript