"PreventionGenetics, part of Exact Sciences"[submitter] AND "TTC28"[ge - ClinVar

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

Search results

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 778199	NM_001145418.2(TTC28):c.7304G>A (p.Arg2435His)	TTC28, TTC28-AS1 (R2435H +3 more)	Single nucleotide variant (missense variant)	TTC28-related condition +1 more	GLikely benign
Select item 3056496	NM_001145418.2(TTC28):c.7271C>G (p.Ala2424Gly)	TTC28, TTC28-AS1 (A2298G +3 more)	Single nucleotide variant (missense variant)	TTC28-related condition	GBenign
Select item 3041446	NM_001145418.2(TTC28):c.7197A>G (p.Pro2399=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3040223	NM_001145418.2(TTC28):c.6816C>T (p.Pro2272=)	TTC28-AS1, TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 785920	NM_001145418.2(TTC28):c.6597G>A (p.Ala2199=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition +1 more	GBenign
Select item 3037151	NM_001145418.2(TTC28):c.6393A>T (p.Ser2131=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition	GBenign
Select item 3029195	NM_001145418.2(TTC28):c.6174G>C (p.Gly2058=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3040953	NM_001145418.2(TTC28):c.5688C>T (p.His1896=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3050362	NM_001145418.2(TTC28):c.5552G>A (p.Arg1851Gln)	TTC28, TTC28-AS1 (R1733Q +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3041167	NM_001145418.2(TTC28):c.5437C>T (p.Arg1813Trp)	TTC28, TTC28-AS1 (R1695W +1 more)	Single nucleotide variant (missense variant)	TTC28-related condition	GLikely benign
Select item 716651	NM_001145418.2(TTC28):c.5372G>A (p.Arg1791Gln)	TTC28, TTC28-AS1 (R1791Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3046441	NM_001145418.2(TTC28):c.5205G>A (p.Pro1735=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 714028	NM_001145418.2(TTC28):c.4962C>T (p.Leu1654=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant +1 more)	TTC28-related condition +1 more	GBenign/Likely benign
Select item 3048180	NM_001145418.2(TTC28):c.4719C>T (p.Phe1573=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3031654	NM_001145418.2(TTC28):c.4319G>C (p.Ser1440Thr)	TTC28, TTC28-AS1 (S1322T +1 more)	Single nucleotide variant (missense variant +1 more)	TTC28-related condition	GUncertain significance
Select item 718658	NM_001145418.2(TTC28):c.4255C>T (p.Arg1419Trp)	TTC28, TTC28-AS1 (R1419W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3030448	NM_001145418.2(TTC28):c.4242C>T (p.Pro1414=)	TTC28, TTC28-AS1	Single nucleotide variant (synonymous variant +1 more)	TTC28-related condition	GLikely benign
Select item 3032467	NM_001145418.2(TTC28):c.3375C>T (p.Leu1125=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3051477	NM_001145418.2(TTC28):c.3015C>T (p.Gly1005=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3038279	NM_001145418.2(TTC28):c.2994C>T (p.Asp998=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GBenign
Select item 3033131	NM_001145418.2(TTC28):c.2829G>A (p.Arg943=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GBenign
Select item 3045306	NM_001145418.2(TTC28):c.2779C>T (p.His927Tyr)	TTC28 (H809Y +1 more)	Single nucleotide variant (missense variant)	TTC28-related condition	GLikely benign
Select item 3048851	NM_001145418.2(TTC28):c.2478G>A (p.Lys826=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 708994	NM_001145418.2(TTC28):c.2382C>T (p.Cys794=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition +1 more	GBenign
Select item 2635079	NM_001145418.2(TTC28):c.1729dup (p.Tyr577fs)	TTC28 (Y459fs +1 more)	Duplication (frameshift variant)	TTC28-related condition	GUncertain significance
Select item 3050967	NM_001145418.2(TTC28):c.1590C>T (p.Tyr530=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3038756	NM_001145418.2(TTC28):c.1005C>T (p.Ala335=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 3046638	NM_001145418.2(TTC28):c.966C>T (p.His322=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition	GLikely benign
Select item 732728	NM_001145418.2(TTC28):c.891C>T (p.His297=)	TTC28	Single nucleotide variant (synonymous variant)	TTC28-related condition +1 more	GLikely benign

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: 29