TMEM68[gene] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153413	GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	LOC126860438, LOC126860439 +3663 more	Copy number gain	See cases	GPathogenic
Select item 154791	GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	AARD, ABRA +3663 more	Copy number gain	See cases	GPathogenic
Select item 59738	GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	AARD, ABRA +3661 more	Copy number gain	See cases	GPathogenic
Select item 57496	GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	LOC105379224, LOC105379230 +3657 more	Copy number gain	See cases	GPathogenic
Select item 149660	GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	AARD, ABRA +3661 more	Copy number gain	See cases	GPathogenic
Select item 153737	GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	LOC129999966, LOC129999967 +3111 more	Copy number gain	See cases	GPathogenic
Select item 150770	GRCh38/hg38 8p12-q12.1(chr8:36580103-59618998)x3	ADAM18, ADAM2 +543 more	Copy number gain	See cases	GPathogenic
Select item 144238	GRCh38/hg38 8q11.1-13.2(chr8:46031334-69303787)x3	ADHFE1, ALKAL1 +491 more	Copy number gain	See cases	GPathogenic
Select item 150723	GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	LOC126860489, LOC126860490 +1963 more	Copy number gain	See cases	GPathogenic
Select item 154575	GRCh38/hg38 8q11.21-12.1(chr8:49471778-57825470)x1	ALKAL1, ATP6V1H +175 more	Copy number loss	See cases	GPathogenic
Select item 155115	GRCh38/hg38 8q11.23-12.3(chr8:53325389-61863018)x1	ASPH, ATP6V1H +228 more	Copy number loss	See cases	GPathogenic
Select item 154925	GRCh38/hg38 8q12.1(chr8:54764950-56785299)x1	CERNA3, CHCHD7 +69 more	Copy number loss	See cases	GPathogenic
Select item 151958	GRCh38/hg38 8q12.1-12.2(chr8:54821357-61146302)x1	BPNT2, CA8 +175 more	Copy number loss	See cases	GPathogenic
Select item 148601	GRCh38/hg38 8q12.1-12.3(chr8:55315854-64952752)x3	ASPH, BHLHE22 +222 more	Copy number gain	See cases	GPathogenic
Select item 60362	GRCh38/hg38 8q12.1(chr8:55423413-58836753)x1	BPNT2, CERNA3 +105 more	Copy number loss	See cases	GPathogenic
Select item 2319377	NM_001286657.2(TMEM68):c.539G>A (p.Arg180Lys)	TMEM68 (R180K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 149469	GRCh38/hg38 8q12.1(chr8:55751116-55937248)x3	LOC116186928, LOC124174256 +29 more	Copy number gain	See cases	GLikely benign
Select item 2483943	NM_001286657.2(TMEM68):c.377T>C (p.Ile126Thr)	TMEM68 (I126T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322253	NM_001286657.2(TMEM68):c.373C>G (p.Leu125Val)	TMEM68 (L11V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3327174	NM_001286657.2(TMEM68):c.343A>G (p.Met115Val)	TMEM68 (M1V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3327172	NM_001286657.2(TMEM68):c.332A>C (p.Glu111Ala)	TMEM68 (E111A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3179618	NM_001286657.2(TMEM68):c.199A>G (p.Thr67Ala)	TMEM68 (T67A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3327175	NM_001286657.2(TMEM68):c.121G>A (p.Ala41Thr)	TMEM68 (A41T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2606268	NM_001286657.2(TMEM68):c.121G>T (p.Ala41Ser)	TMEM68 (A41S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3327173	NM_001286657.2(TMEM68):c.120T>G (p.Phe40Leu)	TMEM68 (F40L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2546728	NM_001286657.2(TMEM68):c.99G>C (p.Gln33His)	TMEM68 (Q33H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3327171	NM_001286657.2(TMEM68):c.67C>T (p.His23Tyr)	TMEM68 (H23Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3179619	NM_001286657.2(TMEM68):c.52A>G (p.Met18Val)	TMEM68 (M18V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3063025	GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	PREX2, PRKDC +240 more	Copy number gain	not specified	GPathogenic
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 1703544	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	AARD, ABRA +665 more	Copy number gain	Polydactyly	GPathogenic
Select item 979233	GRCh37/hg19 8q12.1(chr8:56550884-56875491)x3	TGS1, TMEM68 +1 more	Copy number gain	not provided	GUncertain significance
Select item 687787	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	BAALC, CNOT7 +665 more	Copy number gain	not provided	GPathogenic
Select item 687493	GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	HSF1, HTRA4 +474 more	Copy number gain	not provided	GPathogenic
Select item 685558	GRCh37/hg19 8p11.22-q12.3(chr8:39555657-64049089)x3	IDO1, IDO2 +78 more	Copy number gain	not provided	GPathogenic
Select item 563496	GRCh37/hg19 8q12.1(chr8:56288969-56854172)x3	XKR4, TGS1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 563467	GRCh37/hg19 8q12.1(chr8:56620114-56870065)x3	TMEM68, LYN +1 more	Copy number gain	not provided	GLikely benign
Select item 443619	GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	AARD, ABRA +593 more	Copy number gain	See cases	GPathogenic
Select item 442201	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	AARD, ABRA +665 more	Copy number gain	See cases	GPathogenic
Select item 442200	GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	FGF20, FGFR1 +665 more	Copy number gain	See cases	GPathogenic
Select item 394884	GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	SCRT1, SCX +665 more	Copy number gain	See cases	GPathogenic
Select item 253344	GRCh37/hg19 8q12.1(chr8:56405320-57358911)x1	TGS1, PENK +8 more	Copy number loss	See cases	GLikely pathogenic
Select item 252969	GRCh37/hg19 8q11.23-12.3(chr8:53436131-65195953)x3	ALKAL1, ASPH +36 more	Copy number gain	See cases	GPathogenic

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Items: 43