MAP2K7[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2274348	NM_145185.4(MAP2K7):c.35G>T (p.Arg12Leu)	MAP2K7 (R12L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330960	NM_145185.4(MAP2K7):c.155G>T (p.Gly52Val)	MAP2K7 (G68V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122789	NM_145185.4(MAP2K7):c.164C>T (p.Ser55Leu)	MAP2K7 (S55L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324159	NM_145185.4(MAP2K7):c.200C>T (p.Pro67Leu)	MAP2K7 (P67L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122790	NM_145185.4(MAP2K7):c.251C>T (p.Pro84Leu)	MAP2K7 (P84L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537381	NM_145185.4(MAP2K7):c.253C>T (p.Arg85Cys)	MAP2K7 (R101C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777407	NM_145185.4(MAP2K7):c.393C>T (p.Cys131=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3122791	NM_145185.4(MAP2K7):c.418C>T (p.Arg140Trp)	MAP2K7 (R183W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555908	NM_145185.4(MAP2K7):c.427G>A (p.Gly143Ser)	MAP2K7 (G159S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347560	NM_145185.4(MAP2K7):c.566A>G (p.Asn189Ser)	MAP2K7 (N205S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710676	NM_145185.4(MAP2K7):c.606C>T (p.Cys202=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2374336	NM_145185.4(MAP2K7):c.626G>A (p.Arg209Gln)	MAP2K7 (R209Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 717082	NM_145185.4(MAP2K7):c.645C>T (p.Pro215=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 710280	NM_145185.4(MAP2K7):c.645C>A (p.Pro215=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2550876	NM_145185.4(MAP2K7):c.649C>T (p.Arg217Cys)	MAP2K7 (R233C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285309	NM_145185.4(MAP2K7):c.650G>A (p.Arg217His)	MAP2K7 (R260H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 438771	NM_145185.4(MAP2K7):c.752T>C (p.Leu251Pro)	MAP2K7 (L251P +1 more)	Single nucleotide variant (missense variant)	Neuroblastoma	Gother
Select item 2408778	NM_145185.4(MAP2K7):c.761G>A (p.Arg254Gln)	MAP2K7 (R297Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 734209	NM_145185.4(MAP2K7):c.795C>T (p.Ser265=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777408	NM_145185.4(MAP2K7):c.831C>T (p.Ser277=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777052	NM_145185.4(MAP2K7):c.855+10G>C	MAP2K7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243653	NM_145185.4(MAP2K7):c.856-19T>C	MAP2K7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 750380	NM_145185.4(MAP2K7):c.856-9C>G	MAP2K7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1222270	NM_145185.4(MAP2K7):c.856-8C>G	MAP2K7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2528913	NM_145185.4(MAP2K7):c.928A>G (p.Ile310Val)	MAP2K7 (I310V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 717113	NM_145185.4(MAP2K7):c.1079+9C>T	MAP2K7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2649185	NM_145185.4(MAP2K7):c.1080-4C>G	MAP2K7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2314510	NM_145185.4(MAP2K7):c.1114A>G (p.Asn372Asp)	MAP2K7 (N388D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292980	NM_145185.4(MAP2K7):c.1172C>T (p.Ala391Val)	MAP2K7 (A391V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596932	NM_145185.4(MAP2K7):c.1202C>T (p.Thr401Ile)	MAP2K7 (T408I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715594	NM_145185.4(MAP2K7):c.1212G>T (p.Pro404=)	MAP2K7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2296381	NM_145185.4(MAP2K7):c.1214G>A (p.Arg405Gln)	MAP2K7 (R421Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348110	NM_145185.4(MAP2K7):c.1232G>T (p.Ser411Ile)	MAP2K7 (S411I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292981	NM_145185.4(MAP2K7):c.1238C>T (p.Pro413Leu)	MAP2K7 (P413L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 34