ClinVar Miner

List of variants in gene SLC14A1 reported as uncertain significance for not specified

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_015865.7(SLC14A1):c.1118A>T (p.Asn373Ile) rs35942326 0.00035
NM_015865.7(SLC14A1):c.62A>G (p.Gln21Arg) rs146079238 0.00031
NM_015865.7(SLC14A1):c.770G>T (p.Cys257Phe) rs201451018 0.00005
NM_015865.7(SLC14A1):c.1121G>A (p.Arg374His) rs374937387 0.00003
NM_015865.7(SLC14A1):c.1111G>A (p.Glu371Lys) rs756254780 0.00002
NM_015865.7(SLC14A1):c.352G>A (p.Ala118Thr) rs778632720 0.00001
NM_015865.7(SLC14A1):c.399G>A (p.Met133Ile) rs768933061 0.00001
NM_015865.7(SLC14A1):c.428T>G (p.Phe143Cys) rs1415543271 0.00001
NM_015865.7(SLC14A1):c.501G>C (p.Met167Ile) rs368758488 0.00001
NM_015865.7(SLC14A1):c.61C>A (p.Gln21Lys) rs765284140 0.00001
NM_015865.7(SLC14A1):c.718T>C (p.Trp240Arg) rs760579000 0.00001
NM_015865.7(SLC14A1):c.742G>A (p.Ala248Thr) rs763095261 0.00001
NM_015865.7(SLC14A1):c.1039C>G (p.Leu347Val) rs759312861
NM_015865.7(SLC14A1):c.137C>A (p.Ala46Asp)
NM_015865.7(SLC14A1):c.219C>A (p.Asn73Lys) rs779835840
NM_015865.7(SLC14A1):c.238C>A (p.Leu80Met)
NM_015865.7(SLC14A1):c.287G>T (p.Gly96Val) rs2047018661
NM_015865.7(SLC14A1):c.313C>G (p.Leu105Val) rs959314162
NM_015865.7(SLC14A1):c.340A>G (p.Arg114Gly)
NM_015865.7(SLC14A1):c.368G>C (p.Gly123Ala)
NM_015865.7(SLC14A1):c.435G>C (p.Trp145Cys)
NM_015865.7(SLC14A1):c.457A>G (p.Met153Val)
NM_015865.7(SLC14A1):c.554C>T (p.Ser185Leu) rs765470894
NM_015865.7(SLC14A1):c.617T>A (p.Ile206Lys)
NM_015865.7(SLC14A1):c.635T>G (p.Ile212Ser)
NM_015865.7(SLC14A1):c.739G>A (p.Gly247Arg) rs2511246675
NM_015865.7(SLC14A1):c.848T>A (p.Phe283Tyr)

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