Related gene-specific medical variations for Gene (Select 9575) - ClinVar

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Links from Gene

Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3267836	NM_004898.4(CLOCK):c.1464G>C (p.Gln488His)	CLOCK, TMEM165 (Q488H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267835	NM_004898.4(CLOCK):c.1246A>G (p.Ser416Gly)	CLOCK, TMEM165 (S416G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267834	NM_004898.4(CLOCK):c.1621A>C (p.Ile541Leu)	CLOCK, TMEM165 (I541L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267828	NM_004898.4(CLOCK):c.1831A>G (p.Met611Val)	CLOCK, TMEM165 (M611V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267827	NM_004898.4(CLOCK):c.1294G>C (p.Ala432Pro)	CLOCK, TMEM165 (A432P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145942	NM_004898.4(CLOCK):c.2186T>C (p.Met729Thr)	CLOCK, TMEM165 (M729T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145941	NM_004898.4(CLOCK):c.2096G>A (p.Arg699Lys)	CLOCK, TMEM165 (R699K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145940	NM_004898.4(CLOCK):c.1820T>G (p.Ile607Ser)	CLOCK, TMEM165 (I607S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145939	NM_004898.4(CLOCK):c.1369A>G (p.Thr457Ala)	CLOCK, TMEM165 (T457A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145938	NM_004898.4(CLOCK):c.1271T>C (p.Phe424Ser)	CLOCK, TMEM165 (F424S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145937	NM_004898.4(CLOCK):c.1157G>A (p.Arg386Gln)	CLOCK, TMEM165 (R386Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512461	NM_004898.4(CLOCK):c.2140G>A (p.Val714Met)	CLOCK, TMEM165 (V714M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495415	NM_004898.4(CLOCK):c.2192T>C (p.Met731Thr)	CLOCK, TMEM165 (M731T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456067	NM_004898.4(CLOCK):c.2017G>A (p.Gly673Arg)	CLOCK, TMEM165 (G673R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405460	NM_004898.4(CLOCK):c.1708T>A (p.Ser570Thr)	CLOCK, TMEM165 (S570T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375953	NM_004898.4(CLOCK):c.1229A>C (p.Asn410Thr)	CLOCK, TMEM165 (N410T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337285	NM_004898.4(CLOCK):c.2426A>G (p.Gln809Arg)	CLOCK, TMEM165 (Q809R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329406	NM_004898.4(CLOCK):c.1628G>A (p.Arg543Gln)	CLOCK, TMEM165 (R543Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317772	NM_004898.4(CLOCK):c.1807C>T (p.Pro603Ser)	CLOCK, TMEM165 (P603S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218547	NM_004898.4(CLOCK):c.1819A>T (p.Ile607Phe)	CLOCK, TMEM165 (I607F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784039	NM_004898.4(CLOCK):c.1206+10T>C	CLOCK, TMEM165	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 722817	NM_004898.4(CLOCK):c.1367C>T (p.Pro456Leu)	CLOCK, TMEM165 (P456L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 711412	NM_004898.4(CLOCK):c.1584C>T (p.Asp528=)	CLOCK, TMEM165	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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Links from Gene

Items: 23