"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1268 - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2778917	NM_003701.4(TNFSF11):c.220-11C>T	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1596545	NM_003701.4(TNFSF11):c.220-9C>T	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2751685	NM_003701.4(TNFSF11):c.220-7T>C	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 312231	NM_003701.4(TNFSF11):c.239C>T (p.Ser80Leu)	LOC126861752, TNFSF11 (S7L +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive osteopetrosis 2 +2 more	GBenign/Likely benign
Select item 2018234	NM_003701.4(TNFSF11):c.246T>C (p.Asp82=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1396652	NM_003701.4(TNFSF11):c.254A>G (p.His85Arg)	LOC126861752, TNFSF11 (H12R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1012150	NM_003701.4(TNFSF11):c.263A>G (p.Tyr88Cys)	LOC126861752, TNFSF11 (Y15C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2115286	NM_003701.4(TNFSF11):c.268A>G (p.Ile90Val)	LOC126861752, TNFSF11 (I90V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2008357	NM_003701.4(TNFSF11):c.291A>C (p.Ala97=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1507289	NM_003701.4(TNFSF11):c.292G>C (p.Asp98His)	LOC126861752, TNFSF11 (D98H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2913780	NM_003701.4(TNFSF11):c.306A>G (p.Thr102=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1414339	NM_003701.4(TNFSF11):c.308C>T (p.Thr103Ile)	LOC126861752, TNFSF11 (T103I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1624527	NM_003701.4(TNFSF11):c.324T>C (p.Asp108=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2044087	NM_003701.4(TNFSF11):c.344C>T (p.Ser115Leu)	LOC126861752, TNFSF11 (S42L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1465276	NM_003701.4(TNFSF11):c.353G>T (p.Arg118Ile)	LOC126861752, TNFSF11 (R118I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1621646	NM_003701.4(TNFSF11):c.354A>G (p.Arg118=)	LOC126861752, TNFSF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2772810	NM_003701.4(TNFSF11):c.387+7C>T	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1926500	NM_003701.4(TNFSF11):c.387+13_387+14delinsGA	LOC126861752, TNFSF11	Indel (intron variant)	not provided	GUncertain significance
Select item 195202	NM_003701.4(TNFSF11):c.387+14G>A	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 2847224	NM_003701.4(TNFSF11):c.387+19T>C	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1933780	NM_003701.4(TNFSF11):c.387+20G>A	LOC126861752, TNFSF11	Single nucleotide variant (intron variant)	not provided	GLikely benign

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Items: 21