Related gene-specific medical variations for Gene (Select 133584) - ClinVar - NCBI

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Links from Gene

Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274744	NM_152403.4(EGFLAM):c.1859C>T (p.Ala620Val)	EGFLAM, EGFLAM-AS1 +1 more (A620V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274742	NM_152403.4(EGFLAM):c.2951C>A (p.Thr984Asn)	EGFLAM, LOC126807367 (T750N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274737	NM_152403.4(EGFLAM):c.2962G>A (p.Asp988Asn)	EGFLAM, LOC126807367 (D754N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087653	NM_152403.4(EGFLAM):c.1990A>C (p.Ile664Leu)	EGFLAM, EGFLAM-AS1 +1 more (I664L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3087652	NM_152403.4(EGFLAM):c.1981T>A (p.Phe661Ile)	EGFLAM, EGFLAM-AS1 +1 more (F661I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3087651	NM_152403.4(EGFLAM):c.1870T>C (p.Trp624Arg)	EGFLAM, EGFLAM-AS1 +1 more (W624R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087649	NM_152403.4(EGFLAM):c.1756G>A (p.Asp586Asn)	EGFLAM-AS1, EGFLAM (D586N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2508711	NM_152403.4(EGFLAM):c.2929G>A (p.Val977Met)	EGFLAM, LOC126807367 (V120M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360494	NM_152403.4(EGFLAM):c.1877T>C (p.Leu626Pro)	EGFLAM, EGFLAM-AS1 +1 more (L392P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356343	NM_152403.4(EGFLAM):c.2929G>T (p.Val977Leu)	EGFLAM, LOC126807367 (V120L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355877	NM_152403.4(EGFLAM):c.2896C>G (p.Leu966Val)	EGFLAM, LOC126807367 (L109V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332763	NM_152403.4(EGFLAM):c.2024T>C (p.Phe675Ser)	EGFLAM, EGFLAM-AS1 +1 more (F441S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2314908	NM_152403.4(EGFLAM):c.2951C>T (p.Thr984Ile)	EGFLAM, LOC126807367 (T127I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303975	NM_152403.4(EGFLAM):c.1998G>C (p.Leu666Phe)	EGFLAM, EGFLAM-AS1 +1 more (L432F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2254544	NM_152403.4(EGFLAM):c.2016G>T (p.Glu672Asp)	EGFLAM, EGFLAM-AS1 +1 more (E672D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance