"Ambry Genetics"[submitter] AND "MS4A6E"[gene] - ClinVar - NCBI

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

Search results

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2358389	NM_139249.4(MS4A6E):c.7T>A (p.Ser3Thr)	MS4A6E (S3T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529909	NM_139249.4(MS4A6E):c.13C>T (p.Pro5Ser)	MS4A6E (P5S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210775	NM_139249.4(MS4A6E):c.23A>G (p.Asn8Ser)	MS4A6E (N8S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324816	NM_139249.4(MS4A6E):c.24T>G (p.Asn8Lys)	MS4A6E (N8K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373786	NM_139249.4(MS4A6E):c.40C>T (p.Leu14Phe)	MS4A6E (L14F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367123	NM_139249.4(MS4A6E):c.59A>G (p.Asn20Ser)	MS4A6E (N20S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3296192	NM_139249.4(MS4A6E):c.82G>A (p.Glu28Lys)	MS4A6E (E28K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2283580	NM_139249.4(MS4A6E):c.118C>T (p.Arg40Cys)	MS4A6E (R40C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389638	NM_139249.4(MS4A6E):c.224C>T (p.Pro75Leu)	MS4A6E (P75L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2477870	NM_139249.4(MS4A6E):c.314C>T (p.Pro105Leu)	MS4A6E (P105L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3210785	NM_139249.4(MS4A6E):c.325G>C (p.Asp109His)	MS4A6E (D109H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371202	NM_139249.4(MS4A6E):c.335G>A (p.Arg112Lys)	MS4A6E (R112K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210787	NM_139249.4(MS4A6E):c.394T>A (p.Phe132Ile)	MS4A6E (F132I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232392	NM_139249.4(MS4A6E):c.425A>G (p.Gln142Arg)	MS4A6E (Q142R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign