"GeneDx"[submitter] AND "INSL3"[gene] - ClinVar - NCBI

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

Search results

Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1174416	NM_005543.4(INSL3):c.*263G>A	INSL3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1249049	NM_005543.4(INSL3):c.191-30C>T	INSL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253265	NM_005543.4(INSL3):c.178A>G (p.Thr60Ala)	INSL3 (T60A)	Single nucleotide variant (missense variant)	Cryptorchidism +1 more	GBenign
Select item 1271020	NM_005543.4(INSL3):c.126A>G (p.Leu42=)	INSL3	Single nucleotide variant (synonymous variant)	Cryptorchidism +1 more	GBenign
Select item 1277901	NM_005543.4(INSL3):c.27G>A (p.Ala9=)	INSL3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1234596	NC_000019.10:g.17821871A>G	INSL3	Single nucleotide variant	not provided	GBenign
Select item 1281516	NC_000019.10:g.17821901del	INSL3	Deletion	not provided	GBenign
Select item 1240624	NC_000019.10:g.17821901_17821902insTTG	INSL3	Insertion	not provided	GBenign
Select item 1237411	NC_000019.10:g.17821906_17821907insA	INSL3	Insertion	not provided	GBenign
Select item 1259437	NC_000019.10:g.17821908T>A	INSL3	Single nucleotide variant	not provided	GBenign
Select item 1265469	NC_000019.10:g.17821909A>T	INSL3	Single nucleotide variant	not provided	GBenign
Select item 1288351	NC_000019.10:g.17821915A>T	INSL3	Single nucleotide variant	not provided	GBenign
Select item 1230160	NC_000019.10:g.17821918A>G	INSL3	Single nucleotide variant	not provided	GBenign