"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC400499" - ClinVar - NCBI

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

Search results

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2646218	NM_001370704.1(LOC400499):c.7047G>A (p.Lys2349=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646219	NM_001370704.1(LOC400499):c.6561G>A (p.Glu2187=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646220	NM_001370704.1(LOC400499):c.6507C>T (p.Ser2169=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646221	NM_001370704.1(LOC400499):c.5877G>A (p.Pro1959=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646222	NM_001370704.1(LOC400499):c.5682C>T (p.Ser1894=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646223	NM_001370704.1(LOC400499):c.5112C>T (p.Asn1704=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646224	NM_001370704.1(LOC400499):c.4364G>A (p.Arg1455Gln)	LOC400499 (R1455Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2646225	NM_001370704.1(LOC400499):c.4266A>G (p.Thr1422=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646226	NM_001370704.1(LOC400499):c.3648C>T (p.Tyr1216=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646227	NM_001370704.1(LOC400499):c.3177C>T (p.His1059=)	LOC101927131, LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646228	NM_001370704.1(LOC400499):c.2691T>C (p.His897=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646229	NM_001370704.1(LOC400499):c.535C>A (p.Arg179=)	LOC400499	Single nucleotide variant (synonymous variant)	not provided	GLikely benign