Related gene-specific medical variations for Gene (Select 5236) - ClinVar

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Items: 79

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3354471	NM_002633.3(PGM1):c.125G>C (p.Ser42Thr)	LOC129930668, PGM1 (S42T)	Single nucleotide variant (missense variant)	PGM1-related disorder	GUncertain significance
Select item 3306003	NM_002633.3(PGM1):c.193T>G (p.Phe65Val)	LOC129930668, PGM1 (F65V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3306002	NM_002633.3(PGM1):c.155G>C (p.Arg52Pro)	LOC129930668, PGM1 (R52P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3247792	NC_000001.10:g.(?_64119983)_(64125346_?)del	PGM1	Deletion	PGM1-congenital disorder of glycosylation	GPathogenic
Select item 3211845	NM_002633.3(PGM1):c.130A>G (p.Ile44Val)	LOC129930668, PGM1 (I44V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3065803	NM_002633.3(PGM1):c.980G>C (p.Gly327Ala)	PGM1 (G130A +2 more)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2920589	NM_002633.3(PGM1):c.108G>A (p.Ala36=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2897490	NM_002633.3(PGM1):c.123G>A (p.Gln41=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2887266	NM_002633.3(PGM1):c.156G>C (p.Arg52=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2821223	NM_002633.3(PGM1):c.51G>C (p.Pro17=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2809146	NM_002633.3(PGM1):c.90G>A (p.Gln30=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2741013	NM_002633.3(PGM1):c.24G>T (p.Lys8Asn)	LOC129930668, PGM1 (K8N)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2729626	NM_002633.3(PGM1):c.180C>T (p.Gly60=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2690669	NM_002633.3(PGM1):c.689G>A (p.Gly230Glu)	PGM1 (G230E +2 more)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GLikely pathogenic
Select item 2603424	NM_002633.3(PGM1):c.143A>G (p.Glu48Gly)	LOC129930668, PGM1 (E48G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2581183	NM_002633.3(PGM1):c.87_94del (p.Phe29fs)	LOC129930668, PGM1 (F29fs)	Deletion (frameshift variant)	PGM1-congenital disorder of glycosylation	GPathogenic
Select item 2476057	NM_002633.3(PGM1):c.56C>G (p.Thr19Arg)	LOC129930668, PGM1 (T19R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2434675	NM_002633.3(PGM1):c.1138G>A (p.Gly380Arg)	PGM1 (G183R +2 more)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2389740	NM_002633.3(PGM1):c.158A>G (p.Gln53Arg)	LOC129930668, PGM1 (Q53R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304561	NM_002633.3(PGM1):c.244G>A (p.Gly82Arg)	LOC129930669, PGM1 (G82R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287194	NM_002633.3(PGM1):c.191G>A (p.Arg64Gln)	LOC129930668, PGM1 (R64Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236593	NM_002633.3(PGM1):c.23A>G (p.Lys8Arg)	LOC129930668, PGM1 (K8R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2180211	NM_002633.3(PGM1):c.120C>G (p.Ile40Met)	LOC129930668, PGM1 (I40M)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2171325	NM_002633.3(PGM1):c.134C>T (p.Ser45Phe)	LOC129930668, PGM1 (S45F)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2163043	NM_002633.3(PGM1):c.60C>T (p.Ser20=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2160644	NM_002633.3(PGM1):c.246G>A (p.Gly82=)	LOC129930669, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2155662	NM_002633.3(PGM1):c.243C>T (p.Asn81=)	LOC129930669, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2151877	NM_002633.3(PGM1):c.119del (p.Ile40fs)	LOC129930668, PGM1 (I40fs)	Deletion (frameshift variant)	PGM1-congenital disorder of glycosylation	GPathogenic
Select item 2140956	NM_002633.3(PGM1):c.246+20_246+21delinsAA	LOC129930669, PGM1	Indel (intron variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2108026	NM_002633.3(PGM1):c.105C>T (p.Tyr35=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2082775	NM_002633.3(PGM1):c.38A>C (p.Gln13Pro)	LOC129930668, PGM1 (Q13P)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2077737	NM_002633.3(PGM1):c.246+8A>G	LOC129930669, PGM1	Single nucleotide variant (intron variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2069140	NM_002633.3(PGM1):c.119T>C (p.Ile40Thr)	LOC129930668, PGM1 (I40T)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 2054172	NM_002633.3(PGM1):c.168G>C (p.Thr56=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2035925	NM_002633.3(PGM1):c.42C>T (p.Asp14=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 2010104	NM_002633.3(PGM1):c.152A>G (p.Gln51Arg)	LOC129930668, PGM1 (Q51R)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1991831	NM_002633.3(PGM1):c.129C>T (p.Ile43=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 1972730	NM_002633.3(PGM1):c.48G>A (p.Lys16=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 1951567	NM_002633.3(PGM1):c.171G>A (p.Leu57=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 1948608	NM_002633.3(PGM1):c.107C>T (p.Ala36Val)	LOC129930668, PGM1 (A36V)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1932812	NM_002633.3(PGM1):c.5T>G (p.Val2Gly)	LOC129930668, PGM1 (V2G)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1914919	NM_002633.3(PGM1):c.246+11C>T	LOC129930669, PGM1	Single nucleotide variant (intron variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 1911641	NM_002633.3(PGM1):c.97G>C (p.Ala33Pro)	LOC129930668, PGM1 (A33P)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1804740	NM_002633.3(PGM1):c.170T>C (p.Leu57Pro)	LOC129930668, PGM1 (L57P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1694516	NM_002633.3(PGM1):c.28_37del (p.Gln10fs)	PGM1, LOC129930668 (Q10fs)	Deletion (frameshift variant)	not provided +1 more	GPathogenic
Select item 1433470	NM_002633.3(PGM1):c.91A>G (p.Ser31Gly)	LOC129930668, PGM1 (S31G)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1423448	NM_002633.3(PGM1):c.125G>A (p.Ser42Asn)	LOC129930668, PGM1 (S42N)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation +1 more	GUncertain significance
Select item 1416374	NM_002633.3(PGM1):c.76G>A (p.Val26Met)	LOC129930668, PGM1 (V26M)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1385170	NM_002633.3(PGM1):c.199A>G (p.Met67Val)	LOC129930668, PGM1 (M67V)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1366132	NM_002633.3(PGM1):c.155G>A (p.Arg52Gln)	LOC129930668, PGM1 (R52Q)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 1340759	GRCh37/hg19 1p31.3(chr1:64102589-64190341)x1	PGM1	Copy number loss	not provided	GLikely benign
Select item 1259045	NM_002633.3(PGM1):c.246+67C>T	LOC129930669, PGM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1216633	NM_002633.3(PGM1):c.246+88C>T	PGM1, LOC129930669	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1204360	NM_002633.3(PGM1):c.246+197C>T	LOC129930669, PGM1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1064684	PGM1, ARG521TER	PGM1	Single nucleotide variant	PGM1-congenital disorder of glycosylation	GPathogenic
Select item 1016026	NM_002633.3(PGM1):c.187G>T (p.Gly63Cys)	LOC129930668, PGM1 (G63C)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 965085	NM_002633.3(PGM1):c.157_158delinsG (p.Gln53fs)	LOC129930668, PGM1 (Q53fs)	Indel (frameshift variant)	not provided +1 more	GPathogenic
Select item 950179	NM_002633.3(PGM1):c.178G>C (p.Gly60Arg)	LOC129930668, PGM1 (G60R)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 937395	NM_002633.3(PGM1):c.138C>A (p.Thr46=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 931787	NM_002633.3(PGM1):c.873+6T>C	PGM1	Single nucleotide variant (intron variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 874605	NM_002633.3(PGM1):c.244G>T (p.Gly82Trp)	LOC129930669, PGM1 (G82W)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 874604	NM_002633.3(PGM1):c.160G>A (p.Glu54Lys)	LOC129930668, PGM1 (E54K)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 874603	NM_002633.3(PGM1):c.107C>A (p.Ala36Glu)	LOC129930668, PGM1 (A36E)	Single nucleotide variant (missense variant)	PGM1-related disorder +2 more	GUncertain significance
Select item 874602	NM_002633.3(PGM1):c.-39C>G	LOC129930668, PGM1	Single nucleotide variant (5 prime UTR variant)	PGM1-congenital disorder of glycosylation	GUncertain significance
Select item 806150	NM_002633.3(PGM1):c.74G>A (p.Arg25Gln)	LOC129930668, PGM1 (R25Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 745911	NM_002633.3(PGM1):c.159G>A (p.Gln53=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 739086	NM_002633.3(PGM1):c.57G>A (p.Thr19=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 704066	NM_002633.3(PGM1):c.12C>A (p.Ile4=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation	GLikely benign
Select item 676174	NM_002633.3(PGM1):c.246+239C>G	LOC129930669, PGM1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 668472	NM_002633.3(PGM1):c.-41G>A	LOC129930668, PGM1	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 663105	NM_002633.3(PGM1):c.87_88del (p.Phe29fs)	LOC129930668, PGM1 (F29fs)	Deletion (frameshift variant)	PGM1-congenital disorder of glycosylation	GPathogenic
Select item 631612	NM_002633.3(PGM1):c.105C>A (p.Tyr35Ter)	LOC129930668, PGM1 (Y35*)	Single nucleotide variant (nonsense)	PGM1-related disorder	GUncertain significance
Select item 511633	NM_002633.3(PGM1):c.64C>T (p.Leu22=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	PGM1-congenital disorder of glycosylation +1 more	GLikely benign
Select item 510436	NM_002633.3(PGM1):c.-49C>G	LOC129930668, PGM1	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 501053	NM_002633.3(PGM1):c.122A>G (p.Gln41Arg)	LOC129930668, PGM1 (Q41R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 384571	NM_002633.3(PGM1):c.18A>G (p.Thr6=)	PGM1, LOC129930668	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 382980	NM_002633.3(PGM1):c.99C>T (p.Ala33=)	LOC129930668, PGM1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 133288	NM_002633.3(PGM1):c.184G>C (p.Asp62His)	LOC129930668, PGM1 (D62H)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation +1 more	GConflicting classifications of pathogenicity
Select item 133287	NM_002633.3(PGM1):c.112A>T (p.Asn38Tyr)	LOC129930668, PGM1 (N38Y)	Single nucleotide variant (missense variant)	PGM1-congenital disorder of glycosylation +1 more	GPathogenic

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Links from Gene

Items: 79