Mutation

Primary Site >> Pancreatic Cancer

Gene >> ABCA12

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	215026910:215026910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>A
AA Mutation	p.Ala364Thr(p.A364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	214974026:214974026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5485G>T
AA Mutation	p.Asp1829Tyr(p.D1829Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	214980581:214980581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754893598
CDS Mutation	c.4642G>A
AA Mutation	p.Ala1548Thr(p.A1548T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	214982318:214982318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763676072
CDS Mutation	c.4448T>C
AA Mutation	p.Met1483Thr(p.M1483T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	214997799:214997799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3190A>C
AA Mutation	p.Ser1064Arg(p.S1064R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	215011630:215011630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558822558
CDS Mutation	c.2141G>A
AA Mutation	p.Arg714Gln(p.R714Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272895
Start	214970372:214970372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191670598
CDS Mutation	c.5591C>T
AA Mutation	p.Pro1864Leu(p.P1864L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272895
Start	214983847:214983847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4182G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000272895
Start	215025677:215025677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>A
AA Mutation	p.Ser428Ter(p.S428*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript