ClinVar Miner

List of variants in gene ATR studied for Seckel syndrome 1

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Total variants: 23
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HGVS dbSNP
NM_001184.4(ATR):c.1350-3T>C rs587783323
NM_001184.4(ATR):c.151+4A>G rs1481733213
NM_001184.4(ATR):c.1903C>T (p.Arg635Ter) rs1378333855
NM_001184.4(ATR):c.2022A>G (p.Gly674=) rs587776690
NM_001184.4(ATR):c.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2634-1G>A rs372271245
NM_001184.4(ATR):c.2688G>A (p.Leu896=) rs117926957
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly) rs149008479
NM_001184.4(ATR):c.3477G>T (p.Met1159Ile) rs587777851
NM_001184.4(ATR):c.3799G>A (p.Val1267Ile) rs377689383
NM_001184.4(ATR):c.4306A>G (p.Asn1436Asp) rs587783328
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp) rs148064542
NM_001184.4(ATR):c.4641+15C>T rs200619976
NM_001184.4(ATR):c.4641+1G>T rs797045403
NM_001184.4(ATR):c.4995G>T (p.Lys1665Asn) rs1553761113
NM_001184.4(ATR):c.5196+1G>A rs1553760567
NM_001184.4(ATR):c.5635G>T (p.Asp1879Tyr) rs387907327
NM_001184.4(ATR):c.5732A>G (p.Asn1911Ser) rs587783334
NM_001184.4(ATR):c.5739-14G>T rs587783335
NM_001184.4(ATR):c.6897+464C>G rs587777852
NM_001184.4(ATR):c.6961T>C (p.Phe2321Leu) rs587783338
NM_001184.4(ATR):c.7041+4G>C rs113544835
NM_001184.4(ATR):c.7725G>A (p.Ala2575=) rs587783340

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