CREB1[gene] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150620	GRCh38/hg38 2q31.3-36.2(chr2:180513793-224302848)x3	INPP1, ITGA4 +1097 more	Copy number gain	See cases	GPathogenic
Select item 59158	GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3	LOC129935343, LOC129935344 +1703 more	Copy number gain	See cases	GPathogenic
Select item 154206	GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3	AAMP, ABCA12 +1687 more	Copy number gain	See cases	GPathogenic
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	LOC129935726, LOC129935727 +1665 more	Copy number gain	See cases	GPathogenic
Select item 152738	GRCh38/hg38 2q32.3-35(chr2:192938826-215705052)x1	ABCA12, ABI2 +509 more	Copy number loss	See cases	GPathogenic
Select item 57419	GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3	LOC129935713, LOC129935714 +1299 more	Copy number gain	See cases	GPathogenic
Select item 155234	GRCh38/hg38 2q33.1-34(chr2:199937273-210031924)x1	ABI2, ADAM23 +298 more	Copy number loss	See cases	GPathogenic
Select item 152538	GRCh38/hg38 2q33.1-34(chr2:199946494-209985195)x1	ABI2, ADAM23 +293 more	Copy number loss	See cases	GPathogenic
Select item 150829	GRCh38/hg38 2q33.3-34(chr2:204906843-210031449)x1	ADAM23, C2orf80 +131 more	Copy number loss	See cases	GPathogenic
Select item 150477	GRCh38/hg38 2q33.3-34(chr2:207058886-211245603)x1	ACADL, C2orf80 +96 more	Copy number loss	See cases	GPathogenic
Select item 2464422	NM_004379.5(CREB1):c.22G>A (p.Glu8Lys)	CREB1 (E8K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375523	NM_004379.5(CREB1):c.67C>G (p.Gln23Glu)	CREB1 (Q23E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545123	NM_004379.5(CREB1):c.89A>G (p.Gln30Arg)	CREB1 (Q30R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077301	NM_004379.5(CREB1):c.137C>T (p.Ala46Val)	CREB1 (A46V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550269	NM_004379.5(CREB1):c.137C>G (p.Ala46Gly)	CREB1 (A46G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 719404	NM_004379.5(CREB1):c.216G>A (p.Ala72=)	CREB1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 718069	NM_004379.5(CREB1):c.243A>G (p.Pro81=)	CREB1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 29670	NM_004379.5(CREB1):c.305A>G (p.Asp102Gly)	CREB1 (D116G +2 more)	Single nucleotide variant (missense variant +1 more)	Variant of unknown significance	GUncertain significance
Select item 2382617	NM_004379.5(CREB1):c.442G>A (p.Ala148Thr)	CREB1 (A162T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248443	NM_004379.5(CREB1):c.448G>T (p.Ala150Ser)	CREB1 (A164S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316558	NM_004379.5(CREB1):c.527C>A (p.Ala176Glu)	CREB1 (A136E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 729120	NM_004379.5(CREB1):c.573A>G (p.Gln191=)	CREB1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 769581	NM_004379.5(CREB1):c.582C>G (p.Thr194=)	CREB1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3077302	NM_004379.5(CREB1):c.775G>A (p.Ala259Thr)	CREB1 (A219T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271415	NM_004379.5(CREB1):c.781C>A (p.Pro261Thr)	CREB1 (P221T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 729121	NM_004379.5(CREB1):c.943C>T (p.Leu315=)	CREB1, METTL21A	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 3062594	GRCh37/hg19 2q32.3-34(chr2:194305623-215261531)x1	ABI2, ACADL +95 more	Copy number loss	not specified	GPathogenic
Select item 3062481	GRCh37/hg19 2q33.2-34(chr2:204110688-211638554)x1	ABI2, ACADL +38 more	Copy number loss	not specified	GPathogenic
Select item 2580353	GRCh37/hg19 2q32.1-36.1(chr2:186698504-223918111)x3	AAMP, ABCA12 +208 more	Copy number gain	See cases	GPathogenic
Select item 1808483	GRCh37/hg19 2q32.2-34(chr2:189909904-209468383)x1	ABI2, ADAM23 +107 more	Copy number loss	not provided	GPathogenic
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1703524	GRCh37/hg19 2q32.1-34(chr2:185697659-213002074)	ABI2, ACADL +127 more	Copy number loss	Chromosome 2q32-q33 deletion syndrome	GPathogenic
Select item 1526943	GRCh37/hg19 2q33.1-34(chr2:200851079-209054267)	ABI2, ADAM23 +58 more	Copy number loss	not specified	GPathogenic
Select item 1526933	GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)	AGPS, ANKAR +217 more	Copy number gain	not specified	GPathogenic
Select item 1511552	NC_000002.11:g.(?_203420070)_(211811277_?)del	ABI2, ACADL +44 more	Deletion	Primary pulmonary hypertension	GUncertain significance
Select item 983184	GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3	AAMP, ABCA12 +384 more	Copy number gain	See cases	GPathogenic
Select item 979400	GRCh37/hg19 2q33.2-34(chr2:204445619-212580788)x1	ACADL, ADAM23 +36 more	Copy number loss	not provided	GPathogenic
Select item 814337	GRCh37/hg19 2q24.2-34(chr2:163233162-211927188)x3	CASP8, CAVIN2 +233 more	Copy number gain	not provided	GPathogenic
Select item 635897	Single allele	ACSL3, ADAM23 +208 more	Duplication	Neurodevelopmental disorder	GPathogenic
Select item 562677	GRCh37/hg19 2q33.3-35(chr2:205169148-219149293)x3	AAMP, ABCA12 +60 more	Copy number gain	not provided	GPathogenic
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	RGPD4, RGPD5 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	IL1F10, IL1R1 +1214 more	Copy number gain	See cases	GPathogenic

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Items: 42