List of variants in gene PIGG reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 27

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001127178.3(PIGG):c.771G>A (p.Thr257=)	rs35496504	0.00322
NM_001127178.3(PIGG):c.2204G>A (p.Arg735Gln)	rs138345843	0.00287
NM_001127178.3(PIGG):c.1628C>G (p.Pro543Arg)	rs112764712	0.00245
NM_001127178.3(PIGG):c.1114+8A>G	rs182522437	0.00233
NM_001127178.3(PIGG):c.1254G>A (p.Thr418=)	rs139518242	0.00227
NM_001127178.3(PIGG):c.750G>A (p.Leu250=)	rs145004132	0.00212
NM_001127178.3(PIGG):c.1387C>G (p.Leu463Val)	rs115766555	0.00164
NM_001127178.3(PIGG):c.1515G>A (p.Trp505Ter)	rs150259543	0.00073
NM_001127178.3(PIGG):c.864T>A (p.Pro288=)	rs145528951	0.00041
NM_001127178.3(PIGG):c.1614+247G>A	rs555564479	0.00017
NM_001127178.3(PIGG):c.2552A>C (p.Gln851Pro)	rs150802299	0.00014
NM_001127178.3(PIGG):c.2232G>A (p.Pro744=)	rs376232301	0.00011
NM_001127178.3(PIGG):c.2180G>A (p.Gly727Glu)	rs201842856	0.00005
NM_001127178.3(PIGG):c.1047A>G (p.Arg349=)	rs1397607565	0.00004
NM_001127178.3(PIGG):c.1461C>T (p.His487=)	rs893004331	0.00004
NM_001127178.3(PIGG):c.165T>A (p.Ser55=)	rs138983583	0.00004
NM_001127178.3(PIGG):c.1806C>T (p.Asp602=)	rs150599490	0.00004
NM_001127178.3(PIGG):c.2237G>A (p.Arg746Gln)	rs962499498	0.00004
NM_001127178.3(PIGG):c.883G>T (p.Ala295Ser)	rs201853289	0.00004
NM_001127178.3(PIGG):c.2625dup (p.Asp876fs)	rs1491240980	0.00001
NM_001127178.3(PIGG):c.2937A>G (p.Arg979=)	rs778211486	0.00001
GRCh37/hg19 4p16.3(chr4:499507-502759)x1
NM_001127178.3(PIGG):c.1020del (p.Gly341fs)	rs1209087083
NM_001127178.3(PIGG):c.1228A>C (p.Arg410=)
NM_001127178.3(PIGG):c.2250G>A (p.Lys750=)
NM_001127178.3(PIGG):c.2805C>A (p.Ile935=)	rs267600179
NM_001127178.3(PIGG):c.785del (p.Leu262fs)	rs2108814954

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.