List of variants in gene ARID1B reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001374828.1(ARID1B):c.5851G>A (p.Glu1951Lys)	rs1451259945	0.00004
NM_001374828.1(ARID1B):c.1319G>C (p.Gly440Ala)	rs1332073619	0.00001
NM_001374828.1(ARID1B):c.1451dup (p.Phe485fs)	rs1554248082
NM_001374828.1(ARID1B):c.2248-2A>G	rs2128462015
NM_001374828.1(ARID1B):c.2440G>T (p.Val814Leu)	rs765365713
NM_001374828.1(ARID1B):c.4263del (p.Gly1422fs)	rs1583491381
NM_001374828.1(ARID1B):c.4299C>A (p.Tyr1433Ter)	rs1583491515
NM_001374828.1(ARID1B):c.4479G>A (p.Pro1493=)	rs797045277
NM_001374828.1(ARID1B):c.5263+1G>T	rs2128377544
NM_001374828.1(ARID1B):c.5365del (p.Ser1789fs)	rs2128385522
NM_001374828.1(ARID1B):c.5652C>G (p.Ser1884Arg)	rs1195428885
NM_001374828.1(ARID1B):c.6793G>A (p.Asp2265Asn)	rs2128398514
NM_001374828.1(ARID1B):c.6896del (p.Gln2299fs)	rs1583518354

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