"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC22A4"[ - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039399	NM_003059.3(SLC22A4):c.-10A>T	SLC22A4	Single nucleotide variant (5 prime UTR variant)	SLC22A4-related condition	GLikely benign
Select item 1878310	NM_003059.3(SLC22A4):c.393+1G>A	SLC22A4	Single nucleotide variant (splice donor variant)	SLC22A4-related condition +1 more	GUncertain significance
Select item 1426958	NM_003059.3(SLC22A4):c.456C>T (p.Gly152=)	MIR3936HG, SLC22A4	Single nucleotide variant (non-coding transcript variant +1 more)	SLC22A4-related condition +1 more	GLikely benign
Select item 785802	NM_003059.3(SLC22A4):c.465C>T (p.Leu155=)	MIR3936HG, SLC22A4	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GBenign
Select item 1615351	NM_003059.3(SLC22A4):c.498-7T>C	MIR3936HG, SLC22A4	Single nucleotide variant (intron variant)	SLC22A4-related condition +1 more	GBenign
Select item 2065067	NM_003059.3(SLC22A4):c.699A>T (p.Leu233Phe)	MIR3936HG, SLC22A4 (L233F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3048998	NM_003059.3(SLC22A4):c.769C>A (p.Arg257=)	MIR3936HG, SLC22A4	Single nucleotide variant (synonymous variant)	SLC22A4-related condition	GLikely benign
Select item 3033025	NM_003059.3(SLC22A4):c.792G>A (p.Thr264=)	MIR3936HG, SLC22A4	Single nucleotide variant (synonymous variant)	SLC22A4-related condition	GLikely benign
Select item 2629323	NM_003059.3(SLC22A4):c.1071T>A (p.Phe357Leu)	MIR3936HG, SLC22A4 (F357L)	Single nucleotide variant (missense variant)	SLC22A4-related condition	GUncertain significance
Select item 2636579	NM_003059.3(SLC22A4):c.1205C>T (p.Ala402Val)	MIR3936HG, SLC22A4 (A402V)	Single nucleotide variant (non-coding transcript variant +1 more)	SLC22A4-related condition	GUncertain significance
Select item 1628142	NM_003059.3(SLC22A4):c.1445-8C>T	MIR3936HG, SLC22A4	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2629254	NM_003059.3(SLC22A4):c.1471A>G (p.Ile491Val)	MIR3936HG, SLC22A4 (I491V)	Single nucleotide variant (missense variant)	SLC22A4-related condition	GUncertain significance
Select item 733605	NM_003059.3(SLC22A4):c.1500T>C (p.Ile500=)	MIR3936HG, SLC22A4	Single nucleotide variant (synonymous variant)	SLC22A4-related condition +1 more	GBenign/Likely benign
Select item 2037451	NM_003059.3(SLC22A4):c.1647T>C (p.Thr549=)	MIR3936HG, SLC22A4	Single nucleotide variant (synonymous variant)	SLC22A4-related condition +1 more	GLikely benign
Select item 3035927	NM_003059.3(SLC22A4):c.*5A>G	MIR3936HG, SLC22A4	Single nucleotide variant (3 prime UTR variant)	SLC22A4-related condition	GLikely benign