Related gene-specific medical variations for Gene (Select 4585) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3234243	NM_018406.7(MUC4):c.12072A>G (p.Ser4024=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3234161	NM_018406.7(MUC4):c.12053C>A (p.Pro4018His)	LOC126806930, MUC4 (P4018H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2672972	NM_018406.7(MUC4):c.12305T>C (p.Leu4102Pro)	LOC126806930, MUC4 (F5884S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2672971	NM_018406.7(MUC4):c.12657A>C (p.Thr4219=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654497	NC_000003.12:g.195817321A>G	MUC4	Single nucleotide variant	not provided	GBenign
Select item 2654389	NM_018406.7(MUC4):c.12078C>T (p.Ser4026=)	LOC126806930, MUC4	Single nucleotide variant (no sequence alteration +2 more)	not provided	GLikely benign
Select item 2654388	NM_018406.7(MUC4):c.12126C>T (p.Ser4042=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654387	NM_018406.7(MUC4):c.12097_12144del (p.Val4033_Pro4048del)	LOC126806930, MUC4	Deletion (inframe_deletion +1 more)	not provided	GLikely benign
Select item 2654386	NM_018406.7(MUC4):c.12256_12257insTCACCAGCC (p.Ala4086delinsValThrSerPro)	LOC126806930, MUC4	Insertion (inframe_indel +1 more)	not provided	GLikely benign
Select item 2654385	NM_018406.7(MUC4):c.12279C>T (p.His4093=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654384	NM_018406.7(MUC4):c.12366C>T (p.Ser4122=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654383	NM_018406.7(MUC4):c.12444C>T (p.Thr4148=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654382	NM_018406.7(MUC4):c.12446T>G (p.Ile4149Ser)	LOC126806930, MUC4 (I4149S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2654381	NM_018406.7(MUC4):c.12472A>G (p.Thr4158Ala)	LOC126806930, MUC4 (T4158A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2654380	NM_018406.7(MUC4):c.12520_12521del (p.Gly4174fs)	LOC126806930, MUC4 (A6020fs +1 more)	Deletion (frameshift variant +1 more)	not provided	GLikely benign
Select item 2654379	NM_018406.7(MUC4):c.12660T>A (p.Gly4220=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654378	NM_018406.7(MUC4):c.12684C>T (p.Thr4228=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2654377	NM_018406.7(MUC4):c.12705A>C (p.Thr4235=)	LOC126806930, MUC4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 403118	NM_018406.7(MUC4):c.12360T>G (p.Ser4120=)	LOC126806930, MUC4	Single nucleotide variant (no sequence alteration +2 more)	not specified	GBenign