ClinVar for Gene (Select 221395) - ClinVar

Links from Gene

Items: 95

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271609	NM_001098518.2(ADGRF5):c.3215C>T (p.Ala1072Val)	ADGRF5 (A1072V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271600	NM_001098518.2(ADGRF5):c.616C>T (p.Arg206Trp)	ADGRF5 (R206W)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3271592	NM_001098518.2(ADGRF5):c.2424G>C (p.Leu808Phe)	ADGRF5 (L808F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271581	NM_001098518.2(ADGRF5):c.1364A>G (p.Tyr455Cys)	ADGRF5 (Y455C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271571	NM_001098518.2(ADGRF5):c.2404A>G (p.Ile802Val)	ADGRF5 (I802V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271560	NM_001098518.2(ADGRF5):c.1804T>C (p.Phe602Leu)	ADGRF5 (F602L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271550	NM_001098518.2(ADGRF5):c.2939G>C (p.Gly980Ala)	ADGRF5 (G980A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271539	NM_001098518.2(ADGRF5):c.2729C>G (p.Ala910Gly)	ADGRF5 (A910G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271528	NM_001098518.2(ADGRF5):c.1256A>G (p.Asp419Gly)	ADGRF5 (D419G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271517	NM_001098518.2(ADGRF5):c.2300C>T (p.Pro767Leu)	ADGRF5 (P767L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271506	NM_001098518.2(ADGRF5):c.2848G>A (p.Gly950Ser)	ADGRF5 (G950S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271495	NM_001098518.2(ADGRF5):c.491G>A (p.Cys164Tyr)	ADGRF5 (C164Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271484	NM_001098518.2(ADGRF5):c.127G>A (p.Gly43Ser)	ADGRF5 (G43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271474	NM_001098518.2(ADGRF5):c.2407C>A (p.Leu803Ile)	ADGRF5 (L803I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271465	NM_001098518.2(ADGRF5):c.902A>G (p.Asn301Ser)	ADGRF5 (N301S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271454	NM_001098518.2(ADGRF5):c.2512T>C (p.Ser838Pro)	ADGRF5 (S838P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085939	NM_001098518.2(ADGRF5):c.937A>G (p.Ile313Val)	ADGRF5 (I313V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085936	NM_001098518.2(ADGRF5):c.785A>G (p.Asp262Gly)	ADGRF5 (D262G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085931	NM_001098518.2(ADGRF5):c.617G>A (p.Arg206Gln)	ADGRF5 (R206Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085927	NM_001098518.2(ADGRF5):c.542G>A (p.Gly181Asp)	ADGRF5 (G181D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085925	NM_001098518.2(ADGRF5):c.506A>T (p.Asp169Val)	ADGRF5 (D169V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085921	NM_001098518.2(ADGRF5):c.424C>T (p.Arg142Cys)	ADGRF5 (R142C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085910	NM_001098518.2(ADGRF5):c.4001C>T (p.Ser1334Phe)	ADGRF5 (S1334F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085906	NM_001098518.2(ADGRF5):c.3992C>T (p.Thr1331Ile)	ADGRF5 (T1331I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085901	NM_001098518.2(ADGRF5):c.386C>T (p.Pro129Leu)	ADGRF5 (P129L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085899	NM_001098518.2(ADGRF5):c.3736G>C (p.Val1246Leu)	ADGRF5 (V1246L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085896	NM_001098518.2(ADGRF5):c.355T>C (p.Trp119Arg)	ADGRF5 (W119R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085891	NM_001098518.2(ADGRF5):c.3457C>T (p.Arg1153Trp)	ADGRF5 (R1153W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085887	NM_001098518.2(ADGRF5):c.3418C>T (p.Leu1140Phe)	ADGRF5 (L1140F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085874	NM_001098518.2(ADGRF5):c.3240A>G (p.Ile1080Met)	ADGRF5 (I1080M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085867	NM_001098518.2(ADGRF5):c.3214G>A (p.Ala1072Thr)	ADGRF5 (A1072T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085861	NM_001098518.2(ADGRF5):c.3044T>C (p.Ile1015Thr)	ADGRF5 (I1015T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085857	NM_001098518.2(ADGRF5):c.3019C>A (p.Leu1007Ile)	ADGRF5 (L1007I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085852	NM_001098518.2(ADGRF5):c.2991G>T (p.Met997Ile)	ADGRF5 (M997I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085844	NM_001098518.2(ADGRF5):c.2780C>T (p.Thr927Ile)	ADGRF5 (T927I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085834	NM_001098518.2(ADGRF5):c.2582G>A (p.Ser861Asn)	ADGRF5 (S861N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085829	NM_001098518.2(ADGRF5):c.2376G>A (p.Met792Ile)	ADGRF5 (M792I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085816	NM_001098518.2(ADGRF5):c.2239A>G (p.Thr747Ala)	ADGRF5 (T747A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085805	NM_001098518.2(ADGRF5):c.2134C>A (p.Gln712Lys)	ADGRF5 (Q712K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085801	NM_001098518.2(ADGRF5):c.2099T>C (p.Ile700Thr)	ADGRF5 (I700T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085790	NM_001098518.2(ADGRF5):c.1789G>C (p.Asp597His)	ADGRF5 (D597H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3085768	NM_001098518.2(ADGRF5):c.1154A>G (p.Asn385Ser)	ADGRF5 (N385S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619278	NM_001098518.2(ADGRF5):c.3250A>T (p.Thr1084Ser)	ADGRF5 (T1084S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618502	NM_001098518.2(ADGRF5):c.747A>C (p.Glu249Asp)	ADGRF5 (E249D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614443	NM_001098518.2(ADGRF5):c.1442C>T (p.Ser481Phe)	ADGRF5 (S481F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590024	NM_001098518.2(ADGRF5):c.4025C>A (p.Ser1342Tyr)	ADGRF5 (S1342Y)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2588006	NM_001098518.2(ADGRF5):c.388C>T (p.Arg130Trp)	ADGRF5 (R130W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551918	NM_001098518.2(ADGRF5):c.238A>G (p.Ile80Val)	ADGRF5 (I80V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546700	NM_001098518.2(ADGRF5):c.3532C>G (p.Pro1178Ala)	ADGRF5 (P1178A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541992	NM_001098518.2(ADGRF5):c.3413G>T (p.Cys1138Phe)	ADGRF5 (C1138F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541376	NM_001098518.2(ADGRF5):c.2686T>G (p.Ser896Ala)	ADGRF5 (S896A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540391	NM_001098518.2(ADGRF5):c.1369G>A (p.Ala457Thr)	ADGRF5 (A457T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534027	NM_001098518.2(ADGRF5):c.1028G>T (p.Gly343Val)	ADGRF5 (G343V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523874	NM_001098518.2(ADGRF5):c.2136G>C (p.Gln712His)	ADGRF5 (Q712H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521360	NM_001098518.2(ADGRF5):c.3325C>T (p.Leu1109Phe)	ADGRF5 (L1109F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516003	NM_001098518.2(ADGRF5):c.268C>T (p.Pro90Ser)	ADGRF5 (P90S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508799	NM_001098518.2(ADGRF5):c.3572T>C (p.Ile1191Thr)	ADGRF5 (I1191T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482730	NM_001098518.2(ADGRF5):c.3122T>C (p.Val1041Ala)	ADGRF5 (V1041A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479147	NM_001098518.2(ADGRF5):c.2269G>C (p.Asp757His)	ADGRF5 (D757H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478910	NM_001098518.2(ADGRF5):c.496C>T (p.Leu166Phe)	ADGRF5 (L166F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478909	NM_001098518.2(ADGRF5):c.2211G>T (p.Lys737Asn)	ADGRF5 (K737N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470975	NM_001098518.2(ADGRF5):c.845T>G (p.Ile282Ser)	ADGRF5 (I282S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463464	NM_001098518.2(ADGRF5):c.3389T>C (p.Ile1130Thr)	ADGRF5 (I1130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399918	NM_001098518.2(ADGRF5):c.122C>T (p.Pro41Leu)	ADGRF5 (P41L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2394964	NM_001098518.2(ADGRF5):c.1655C>T (p.Ser552Leu)	ADGRF5 (S552L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393121	NM_001098518.2(ADGRF5):c.1802C>T (p.Thr601Ile)	ADGRF5 (T601I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384370	NM_001098518.2(ADGRF5):c.3298G>A (p.Val1100Ile)	ADGRF5 (V1100I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381273	NM_001098518.2(ADGRF5):c.1852A>G (p.Lys618Glu)	ADGRF5 (K618E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373280	NM_001098518.2(ADGRF5):c.2851G>A (p.Glu951Lys)	ADGRF5 (E951K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2370909	NM_001098518.2(ADGRF5):c.2738T>G (p.Ile913Ser)	ADGRF5 (I913S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369390	NM_001098518.2(ADGRF5):c.295A>G (p.Ile99Val)	ADGRF5 (I99V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360147	NM_001098518.2(ADGRF5):c.2795C>T (p.Thr932Ile)	ADGRF5 (T932I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2355934	NM_001098518.2(ADGRF5):c.3662T>C (p.Ile1221Thr)	ADGRF5 (I1221T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350677	NM_001098518.2(ADGRF5):c.3247A>C (p.Lys1083Gln)	ADGRF5 (K1083Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338927	NM_001098518.2(ADGRF5):c.3460G>A (p.Glu1154Lys)	ADGRF5 (E1154K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328875	NM_001098518.2(ADGRF5):c.2831A>G (p.Asn944Ser)	ADGRF5 (N944S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313158	NM_001098518.2(ADGRF5):c.3233G>A (p.Arg1078His)	ADGRF5 (R1078H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2307875	NM_001098518.2(ADGRF5):c.1416T>A (p.Asn472Lys)	ADGRF5 (N472K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303913	NM_001098518.2(ADGRF5):c.484C>A (p.Pro162Thr)	ADGRF5 (P162T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291369	NM_001098518.2(ADGRF5):c.3948G>T (p.Leu1316Phe)	ADGRF5 (L1316F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275964	NM_001098518.2(ADGRF5):c.2334T>A (p.Asp778Glu)	ADGRF5 (D778E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268988	NM_001098518.2(ADGRF5):c.1319C>T (p.Ser440Leu)	ADGRF5 (S440L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254486	NM_001098518.2(ADGRF5):c.553G>C (p.Asp185His)	ADGRF5 (D185H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245816	NM_001098518.2(ADGRF5):c.913C>T (p.Arg305Cys)	ADGRF5 (R305C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227002	NM_001098518.2(ADGRF5):c.112G>C (p.Glu38Gln)	ADGRF5 (E38Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226712	NM_001098518.2(ADGRF5):c.1556C>G (p.Thr519Arg)	ADGRF5 (T519R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213569	NM_001098518.2(ADGRF5):c.2383G>A (p.Val795Met)	ADGRF5 (V795M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1676306	GRCh37/hg19 6p21.1-q12(chr6:43636308-64947206)x3	PAQR8, PGK2 +92 more	Copy number gain	not provided	GLikely pathogenic
Select item 1527236	GRCh37/hg19 6p21.1-12.3(chr6:43636308-50947320)	ADGRF5, ANKRD66 +50 more	Copy number loss	not specified	GPathogenic
Select item 625706	GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367)	ERVH-3, ETV7 +427 more	Copy number gain	not provided	GPathogenic
Select item 563178	GRCh37/hg19 6p12.3(chr6:46717940-46925746)x3	ANKRD66, MEP1A +1 more	Copy number gain	not provided	GLikely benign
Select item 443497	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	AARS2, ABCC10 +1028 more	Copy number gain	See cases	GPathogenic
Select item 443496	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	RING1, RIOK1 +1028 more	Copy number gain	See cases	GPathogenic
Select item 149301	GRCh38/hg38 6p21.1-12.1(chr6:45681671-54212044)x1	GSTA3, GSTA4 +228 more	Copy number loss	See cases	GPathogenic
Select item 146275	GRCh38/hg38 6p21.1-12.3(chr6:44985760-47986838)x3	ADGRF1, ADGRF2 +78 more	Copy number gain	See cases	GLikely pathogenic

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Links from Gene

Items: 95