"Genome-Nilou Lab"[submitter] AND "ANLN"[gene] - ClinVar

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

Search results

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1165102	NM_018685.5(ANLN):c.100A>G (p.Met34Val)	ANLN (M34V)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis 8 +1 more	GBenign/Likely benign
Select item 1612035	NM_018685.5(ANLN):c.173-16A>G	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1166060	NM_018685.5(ANLN):c.194C>G (p.Ser65Trp)	ANLN (S65W)	Single nucleotide variant (missense variant)	Focal segmental glomerulosclerosis 8 +1 more	GBenign
Select item 261050	NM_018685.5(ANLN):c.553A>C (p.Arg185=)	ANLN	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 261051	NM_018685.5(ANLN):c.554G>A (p.Arg185Lys)	ANLN (R185K)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 1166061	NM_018685.5(ANLN):c.819A>G (p.Leu273=)	ANLN	Single nucleotide variant (synonymous variant)	Focal segmental glomerulosclerosis 8 +1 more	GBenign
Select item 1243870	NM_018685.5(ANLN):c.874-56A>G	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 261052	NM_018685.5(ANLN):c.883_885dup (p.Ser295dup)	ANLN	Duplication (inframe_insertion)	not specified +2 more	GBenign
Select item 1273279	NM_018685.5(ANLN):c.1096+35T>C	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1169283	NM_018685.5(ANLN):c.1245C>T (p.Asp415=)	ANLN	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1166062	NM_018685.5(ANLN):c.1506T>C (p.Ser502=)	ANLN	Single nucleotide variant (synonymous variant)	Focal segmental glomerulosclerosis 8 +1 more	GBenign
Select item 1281119	NM_018685.5(ANLN):c.1634-25G>A	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1170048	NM_018685.5(ANLN):c.1686G>A (p.Ser562=)	ANLN	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 737696	NM_018685.5(ANLN):c.1848A>G (p.Thr616=)	ANLN	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1693174	NM_018685.5(ANLN):c.2163+69del	ANLN	Deletion (intron variant)	Focal segmental glomerulosclerosis 8	GBenign
Select item 1290524	NM_018685.5(ANLN):c.2164-24T>C	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1242853	NM_018685.5(ANLN):c.2300-37G>A	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1286858	NM_018685.5(ANLN):c.2749-54T>C	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1693175	NM_018685.5(ANLN):c.2749-3dup	ANLN	Duplication (intron variant)	Focal segmental glomerulosclerosis 8	GBenign
Select item 1693176	NM_018685.5(ANLN):c.2749-3del	ANLN	Deletion (intron variant)	Focal segmental glomerulosclerosis 8	GBenign
Select item 1190421	NM_018685.5(ANLN):c.2770+69A>G	ANLN	Single nucleotide variant (intron variant)	Focal segmental glomerulosclerosis 8 +1 more	GBenign/Likely benign
Select item 1273916	NM_018685.5(ANLN):c.2883+32T>G	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1247391	NM_018685.5(ANLN):c.3251+31A>G	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1274511	NM_018685.5(ANLN):c.3252-41G>A	ANLN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1257449	NM_018685.5(ANLN):c.*3C>T	ANLN	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign

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: 25