ClinVar Miner

List of variants in gene SGCG reported as benign for not provided

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Gene type:
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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_000231.3(SGCG):c.703-53C>T rs9510700 0.77702
NM_000231.3(SGCG):c.196-282A>T rs9510643 0.66038
NM_000231.3(SGCG):c.505+335T>C rs9317612 0.63539
NM_000231.3(SGCG):c.312T>G (p.Leu104=) rs1800351 0.47318
NM_000231.3(SGCG):c.579-28T>G rs1536727 0.42785
NM_000231.3(SGCG):c.579-30T>G rs1536726 0.40128
NM_000231.3(SGCG):c.579-32T>G rs1536725 0.39650
NM_000231.3(SGCG):c.578+281T>C rs4411362 0.35909
NM_000231.3(SGCG):c.196-281A>T rs9510644 0.30340
NM_000231.3(SGCG):c.505+149T>C rs61946706 0.19761
NM_000231.3(SGCG):c.579-22del rs138499218 0.17470
NM_000231.3(SGCG):c.860= (p.Asn287=) rs1800354 0.16253
NM_000231.3(SGCG):c.196-197G>C rs7994953 0.15280
NM_000231.3(SGCG):c.228T>C (p.Asp76=) rs1800350 0.15152
NM_000231.3(SGCG):c.-88G>A rs4770403 0.15108
NM_000231.3(SGCG):c.297+63A>C rs4769246 0.14951
NM_000231.3(SGCG):c.386-30A>G rs66844808 0.10864
NM_000231.3(SGCG):c.505+83G>T rs17374896 0.08156
NM_000231.3(SGCG):c.702+252G>T rs4770431 0.06186
NM_000231.3(SGCG):c.702+326C>T rs4770432 0.06181
NM_000231.3(SGCG):c.385+164G>A rs111626620 0.04666
NM_000231.3(SGCG):c.578+145G>C rs41283950 0.03353
NM_000231.3(SGCG):c.297+108C>T rs17078517 0.03161
NM_000231.3(SGCG):c.505+46T>A rs17078558 0.02013
NM_000231.3(SGCG):c.435C>T (p.Asn145=) rs35628352 0.00973
NM_000231.3(SGCG):c.-6T>C rs141771521 0.00749
GRCh37/hg19 13q12.12(chr13:23760371-23766935)x1
NM_000231.3(SGCG):c.196-125_196-124insTTTA rs58174484
NM_000231.3(SGCG):c.196-300C>G rs71429830
NM_000231.3(SGCG):c.298-248del rs79337752
NM_000231.3(SGCG):c.385+147C>A rs113882306
NM_000231.3(SGCG):c.505+126_505+139del rs141669762
NM_000231.3(SGCG):c.579-22G>T rs111358030
NM_000231.3(SGCG):c.579-23del rs67528585
NM_000231.3(SGCG):c.579-23dup rs67528585
NM_000231.3(SGCG):c.579-24T>G rs1536729
NM_000231.3(SGCG):c.579-24_579-23dup rs67528585
NM_000231.3(SGCG):c.579-26T>G rs1536728

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