"PreventionGenetics, part of Exact Sciences"[submitter] AND "CCAR2"[ge - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051469	NM_001393997.1(CCAR2):c.33G>A (p.Pro11=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3059932	NM_001393997.1(CCAR2):c.84C>T (p.Gly28=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 3059619	NM_001393997.1(CCAR2):c.150+8C>G	CCAR2	Single nucleotide variant (intron variant)	CCAR2-related disorder	GBenign
Select item 3053112	NM_001393997.1(CCAR2):c.519T>G (p.Leu173=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3056349	NM_001393997.1(CCAR2):c.705-8dup	CCAR2	Duplication (intron variant)	CCAR2-related disorder	GLikely benign
Select item 3048593	NM_001393997.1(CCAR2):c.876C>T (p.Asp292=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3060085	NM_001393997.1(CCAR2):c.924G>A (p.Ser308=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 3041917	NM_001393997.1(CCAR2):c.1014G>A (p.Thr338=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3040793	NM_001393997.1(CCAR2):c.1062A>G (p.Glu354=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3058620	NM_001393997.1(CCAR2):c.1116C>T (p.Asp372=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3037246	NM_001393997.1(CCAR2):c.1218C>T (p.Ala406=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 3036073	NM_001393997.1(CCAR2):c.1253G>A (p.Arg418Gln)	CCAR2 (R418Q)	Single nucleotide variant (missense variant)	CCAR2-related disorder	GLikely benign
Select item 3059635	NM_001393997.1(CCAR2):c.1407T>C (p.Asp469=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 3044821	NM_001393997.1(CCAR2):c.1479G>A (p.Thr493=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3049038	NM_001393997.1(CCAR2):c.1530C>T (p.Ile510=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3060419	NM_001393997.1(CCAR2):c.1609-5A>G	CCAR2	Single nucleotide variant (intron variant)	CCAR2-related disorder	GBenign
Select item 3041953	NM_001393997.1(CCAR2):c.1730A>C (p.Glu577Ala)	CCAR2 (E577A)	Single nucleotide variant (missense variant)	CCAR2-related disorder	GLikely benign
Select item 3038827	NM_001393997.1(CCAR2):c.1809G>C (p.Gln603His)	CCAR2 (Q603H)	Single nucleotide variant (missense variant)	CCAR2-related disorder	GBenign
Select item 3039673	NM_001393997.1(CCAR2):c.1821G>A (p.Pro607=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 2658472	NM_001393997.1(CCAR2):c.1845+3G>A	CCAR2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 3035618	NM_001393997.1(CCAR2):c.1911C>T (p.Gly637=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 719716	NM_001393997.1(CCAR2):c.2074-8C>T	CCAR2	Single nucleotide variant (intron variant)	CCAR2-related disorder +1 more	GBenign
Select item 3044794	NM_001393997.1(CCAR2):c.2316C>T (p.Pro772=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3045813	NM_001393997.1(CCAR2):c.2373G>A (p.Lys791=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign
Select item 3043228	NM_001393997.1(CCAR2):c.2457G>A (p.Ala819=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GBenign
Select item 3048106	NM_001393997.1(CCAR2):c.2522-3C>T	CCAR2	Single nucleotide variant (intron variant)	CCAR2-related disorder	GLikely benign
Select item 3048365	NM_001393997.1(CCAR2):c.2541C>T (p.Phe847=)	CCAR2	Single nucleotide variant (synonymous variant)	CCAR2-related disorder	GLikely benign

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Items: 27