"PreventionGenetics, part of Exact Sciences"[submitter] AND "TEX14"[ge - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060778	NM_031272.5(TEX14):c.4227A>G (p.Glu1409=)	TEX14	Single nucleotide variant (synonymous variant)	TEX14-related disorder	GBenign
Select item 3059694	NM_031272.5(TEX14):c.4173A>G (p.Lys1391=)	TEX14	Single nucleotide variant (synonymous variant)	TEX14-related disorder	GBenign
Select item 3043470	NM_031272.5(TEX14):c.4158-10G>A	TEX14	Single nucleotide variant (intron variant)	TEX14-related disorder	GLikely benign
Select item 3058843	NM_031272.5(TEX14):c.3963T>C (p.Asn1321=)	TEX14	Single nucleotide variant (synonymous variant)	TEX14-related disorder	GBenign
Select item 3061002	NM_031272.5(TEX14):c.3172-1926G>A	TEX14 (G1082D +1 more)	Single nucleotide variant (missense variant +1 more)	TEX14-related disorder	GBenign
Select item 3042476	NM_031272.5(TEX14):c.2877C>T (p.Ser959=)	TEX14	Single nucleotide variant (synonymous variant)	TEX14-related disorder	GLikely benign
Select item 3049605	NM_031272.5(TEX14):c.2788+10_2788+11del	TEX14	Deletion (intron variant)	TEX14-related disorder	GLikely benign
Select item 3060802	NM_031272.5(TEX14):c.2338A>G (p.Asn780Asp)	TEX14 (N780D +1 more)	Single nucleotide variant (missense variant)	TEX14-related disorder	GBenign
Select item 3038862	NM_031272.5(TEX14):c.2218A>G (p.Ile740Val)	TEX14 (I740V +1 more)	Single nucleotide variant (missense variant)	TEX14-related disorder	GLikely benign
Select item 3055939	NM_031272.5(TEX14):c.1978A>G (p.Met660Val)	TEX14 (M660V +1 more)	Single nucleotide variant (missense variant)	TEX14-related disorder	GLikely benign
Select item 732060	NM_031272.5(TEX14):c.1384G>T (p.Val462Leu)	TEX14 (V462L +1 more)	Single nucleotide variant (missense variant)	TEX14-related disorder +1 more	GBenign
Select item 3049233	NM_031272.5(TEX14):c.1251C>T (p.Ala417=)	TEX14	Single nucleotide variant (synonymous variant)	TEX14-related disorder	GLikely benign
Select item 3051860	NM_031272.5(TEX14):c.1185-5C>T	TEX14	Single nucleotide variant (intron variant)	TEX14-related disorder	GLikely benign
Select item 3059541	NM_031272.5(TEX14):c.939A>G (p.Leu313=)	TEX14	Single nucleotide variant (synonymous variant)	TEX14-related disorder	GBenign
Select item 3056149	NM_031272.5(TEX14):c.637-11C>A	TEX14 (P215H)	Single nucleotide variant (missense variant +1 more)	TEX14-related disorder	GBenign