"PreventionGenetics, part of Exact Sciences"[submitter] AND "MAP3K6"[g - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 782369	NM_004672.5(MAP3K6):c.3747C>T (p.Leu1249=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder +1 more	GBenign
Select item 3055994	NM_004672.5(MAP3K6):c.3698G>C (p.Gly1233Ala)	MAP3K6 (G1225A +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3057500	NM_004672.5(MAP3K6):c.3530G>A (p.Arg1177His)	MAP3K6 (R1169H +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder +1 more	GLikely benign
Select item 2638557	NM_004672.5(MAP3K6):c.3373_3375del (p.Lys1125del)	MAP3K6 (K1117del +1 more)	Deletion (inframe_deletion)	MAP3K6-related disorder +1 more	GBenign
Select item 3037546	NM_004672.5(MAP3K6):c.3259-10C>T	MAP3K6	Single nucleotide variant (intron variant)	MAP3K6-related disorder	GBenign
Select item 3056146	NM_004672.5(MAP3K6):c.3181G>A (p.Ala1061Thr)	MAP3K6 (A1053T +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 3038494	NM_004672.5(MAP3K6):c.3070A>G (p.Lys1024Glu)	MAP3K6 (K1016E +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3031754	NM_004672.5(MAP3K6):c.2872C>A (p.Pro958Thr)	MAP3K6 (P950T +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 2638558	NM_004672.5(MAP3K6):c.2837C>T (p.Pro946Leu)	MAP3K6 (P938L +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder +1 more	GBenign/Likely benign
Select item 3053182	NM_004672.5(MAP3K6):c.2751C>T (p.Ser917=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder	GLikely benign
Select item 3056439	NM_004672.5(MAP3K6):c.2738G>A (p.Arg913His)	MAP3K6 (R905H +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3056282	NM_004672.5(MAP3K6):c.2584-6C>T	MAP3K6	Single nucleotide variant (intron variant)	MAP3K6-related disorder	GBenign
Select item 3048868	NM_004672.5(MAP3K6):c.2002C>G (p.Arg668Gly)	MAP3K6 (R660G +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 403071	NM_004672.5(MAP3K6):c.1866C>A (p.Asn622Lys)	MAP3K6 (N622K +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 775526	NM_004672.5(MAP3K6):c.1495C>T (p.Arg499Cys)	MAP3K6 (R499C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3035484	NM_004672.5(MAP3K6):c.1467C>T (p.Pro489=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder	GLikely benign
Select item 3037710	NM_004672.5(MAP3K6):c.1415+9C>T	MAP3K6	Single nucleotide variant (intron variant)	MAP3K6-related disorder	GLikely benign
Select item 3059762	NM_004672.5(MAP3K6):c.1364C>T (p.Thr455Ile)	MAP3K6 (T447I +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 718894	NM_004672.5(MAP3K6):c.1256-2A>G	MAP3K6	Single nucleotide variant (splice acceptor variant)	MAP3K6-related disorder +1 more	GLikely benign
Select item 718726	NM_004672.5(MAP3K6):c.1215C>T (p.Ala405=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder +1 more	GBenign
Select item 733210	NM_004672.5(MAP3K6):c.1182A>G (p.Ser394=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder +1 more	GLikely benign
Select item 3042635	NM_004672.5(MAP3K6):c.1162G>A (p.Val388Ile)	MAP3K6 (V380I +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 3038039	NM_004672.5(MAP3K6):c.1124G>A (p.Arg375Gln)	MAP3K6 (R367Q +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 733211	NM_004672.5(MAP3K6):c.744G>A (p.Glu248=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder +1 more	GLikely benign
Select item 2638560	NM_004672.5(MAP3K6):c.738G>A (p.Ala246=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder +1 more	GLikely benign
Select item 782682	NM_004672.5(MAP3K6):c.620T>G (p.Val207Gly)	MAP3K6 (V199G +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder +1 more	GBenign
Select item 3055009	NM_004672.5(MAP3K6):c.607G>A (p.Val203Ile)	MAP3K6 (V195I +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3050855	NM_004672.5(MAP3K6):c.598G>T (p.Asp200Tyr)	MAP3K6 (D192Y +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 3038960	NM_004672.5(MAP3K6):c.318T>C (p.Ala106=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder	GLikely benign

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Items: 29