"PreventionGenetics, part of Exact Sciences"[submitter] AND "KDM3B"[ge - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055328	NM_016604.4(KDM3B):c.13G>A (p.Ala5Thr)	KDM3B, LOC129994737 (A5T)	Single nucleotide variant (missense variant)	KDM3B-related condition	GBenign
Select item 1227741	NM_016604.4(KDM3B):c.264C>T (p.Ile88=)	KDM3B	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 2632477	NM_016604.4(KDM3B):c.361A>G (p.Thr121Ala)	KDM3B (T121A)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 2634040	NM_016604.4(KDM3B):c.486T>G (p.Asp162Glu)	KDM3B (D162E)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 2634493	NM_016604.4(KDM3B):c.509A>G (p.Glu170Gly)	KDM3B (E170G)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3044100	NM_016604.4(KDM3B):c.580+7A>G	KDM3B	Single nucleotide variant (intron variant)	KDM3B-related condition	GLikely benign
Select item 758204	NM_016604.4(KDM3B):c.580+8C>T	KDM3B	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3031870	NM_016604.4(KDM3B):c.693G>A (p.Val231=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 1300056	NM_016604.4(KDM3B):c.714G>A (p.Glu238=)	KDM3B	Single nucleotide variant (synonymous variant)	Diets-Jongmans syndrome +1 more	GBenign
Select item 789583	NM_016604.4(KDM3B):c.804A>G (p.Lys268=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition +1 more	GLikely benign
Select item 3038562	NM_016604.4(KDM3B):c.810C>T (p.Ser270=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 2633375	NM_016604.4(KDM3B):c.847G>C (p.Asp283His)	KDM3B (D283H)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 2636967	NM_016604.4(KDM3B):c.880G>C (p.Gly294Arg)	KDM3B (G294R)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3046801	NM_016604.4(KDM3B):c.1028C>T (p.Pro343Leu)	KDM3B (P343L)	Single nucleotide variant (missense variant)	KDM3B-related condition	GLikely benign
Select item 2263415	NM_016604.4(KDM3B):c.1060A>G (p.Ile354Val)	KDM3B (I354V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 3046913	NM_016604.4(KDM3B):c.1134A>T (p.Thr378=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 3032134	NM_016604.4(KDM3B):c.1177C>T (p.Pro393Ser)	KDM3B (P393S)	Single nucleotide variant (missense variant)	KDM3B-related condition	GLikely benign
Select item 2636669	NM_016604.4(KDM3B):c.1204G>A (p.Glu402Lys)	KDM3B (E402K)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3036734	NM_016604.4(KDM3B):c.1225A>C (p.Thr409Pro)	KDM3B (T409P)	Single nucleotide variant (missense variant)	KDM3B-related condition	GLikely benign
Select item 2636771	NM_016604.4(KDM3B):c.1231G>C (p.Glu411Gln)	KDM3B (E411Q)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3046659	NM_016604.4(KDM3B):c.1259C>G (p.Ser420Cys)	KDM3B (S420C)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3032202	NM_016604.4(KDM3B):c.1312G>A (p.Asp438Asn)	KDM3B (D438N)	Single nucleotide variant (missense variant)	KDM3B-related condition	GLikely benign
Select item 3051778	NM_016604.4(KDM3B):c.1342G>C (p.Glu448Gln)	KDM3B (E448Q)	Single nucleotide variant (missense variant)	KDM3B-related condition	GLikely benign
Select item 3051041	NM_016604.4(KDM3B):c.1371C>T (p.Ala457=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 2655716	NM_016604.4(KDM3B):c.1437A>G (p.Ser479=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition +1 more	GLikely benign
Select item 3049377	NM_016604.4(KDM3B):c.1536A>G (p.Ala512=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 2655717	NM_016604.4(KDM3B):c.1720G>A (p.Val574Ile)	KDM3B (V574I)	Single nucleotide variant (missense variant)	KDM3B-related condition +1 more	GConflicting classifications of pathogenicity
Select item 715401	NM_016604.4(KDM3B):c.1848G>T (p.Glu616Asp)	KDM3B (E616D)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 2633883	NM_016604.4(KDM3B):c.2014C>G (p.Pro672Ala)	KDM3B (P672A)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 2655718	NM_016604.4(KDM3B):c.2340G>A (p.Pro780=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition +1 more	GBenign/Likely benign
Select item 784629	NM_016604.4(KDM3B):c.2430G>A (p.Ser810=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition +1 more	GBenign/Likely benign
Select item 2655719	NM_016604.4(KDM3B):c.2543A>G (p.Asn848Ser)	KDM3B (N848S)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 2636317	NM_016604.4(KDM3B):c.2594C>T (p.Ala865Val)	KDM3B (A865V)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3033925	NM_016604.4(KDM3B):c.2717A>T (p.Asn906Ile)	KDM3B (N906I)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3056882	NM_016604.4(KDM3B):c.2856A>G (p.Val952=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GBenign
Select item 2636608	NM_016604.4(KDM3B):c.3272A>C (p.Glu1091Ala)	KDM3B (E1091A)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 2655721	NM_016604.4(KDM3B):c.3452C>G (p.Pro1151Arg)	KDM3B (P1151R)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 1300058	NM_016604.4(KDM3B):c.3489T>C (p.Gly1163=)	KDM3B	Single nucleotide variant (synonymous variant)	Diets-Jongmans syndrome +2 more	GBenign
Select item 2635181	NM_016604.4(KDM3B):c.3493G>A (p.Gly1165Arg)	KDM3B (G1165R)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 776067	NM_016604.4(KDM3B):c.3505C>T (p.Pro1169Ser)	KDM3B (P1169S)	Single nucleotide variant (missense variant)	KDM3B-related condition +1 more	GBenign
Select item 719430	NM_016604.4(KDM3B):c.3592G>T (p.Ala1198Ser)	KDM3B (A1198S)	Single nucleotide variant (missense variant)	KDM3B-related condition +1 more	GBenign
Select item 1695140	NM_016604.4(KDM3B):c.3903G>A (p.Pro1301=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition +1 more	GLikely benign
Select item 2630664	NM_016604.4(KDM3B):c.3950del (p.Pro1317fs)	KDM3B (P1317fs)	Deletion (frameshift variant)	KDM3B-related condition	GLikely pathogenic
Select item 3047398	NM_016604.4(KDM3B):c.3992G>T (p.Ser1331Ile)	KDM3B (S1331I)	Single nucleotide variant (missense variant)	KDM3B-related condition +1 more	GLikely benign
Select item 2630417	NM_016604.4(KDM3B):c.4070G>A (p.Cys1357Tyr)	KDM3B (C1357Y)	Single nucleotide variant (missense variant)	KDM3B-related condition	GUncertain significance
Select item 3050957	NM_016604.4(KDM3B):c.4149C>T (p.Ser1383=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 3058258	NM_016604.4(KDM3B):c.4194C>T (p.Asn1398=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 3042492	NM_016604.4(KDM3B):c.4419A>G (p.Leu1473=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GLikely benign
Select item 713346	NM_016604.4(KDM3B):c.4776G>A (p.Glu1592=)	KDM3B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3056364	NM_016604.4(KDM3B):c.4893+9C>T	KDM3B	Single nucleotide variant (intron variant)	KDM3B-related condition	GBenign
Select item 3055794	NM_016604.4(KDM3B):c.5022G>A (p.Val1674=)	KDM3B	Single nucleotide variant (synonymous variant)	KDM3B-related condition	GBenign

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Items: 51