ClinVar Miner

List of variants in gene CHD8 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 123
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001170629.2(CHD8):c.3477G>A (p.Val1159=) rs8022395 0.92426
NM_001170629.2(CHD8):c.6468+54G>T rs7152833 0.85917
NM_001170629.2(CHD8):c.5052-73G>T rs10134108 0.80476
NM_001170629.2(CHD8):c.2731-296A>G rs7147024 0.80426
NM_001170629.2(CHD8):c.2908-45C>G rs7155123 0.80426
NM_001170629.2(CHD8):c.5128-205G>A rs1952554 0.79871
NM_001170629.2(CHD8):c.3308-177A>C rs8011945 0.79828
NM_001170629.2(CHD8):c.7182+26del rs35057134 0.26916
NM_001170629.2(CHD8):c.172G>A (p.Val58Met) rs10467770 0.25299
NM_001170629.2(CHD8):c.1601+74T>G rs8015402 0.14733
NM_001170629.2(CHD8):c.1602-125A>G rs17197114 0.12764
NM_001170629.2(CHD8):c.844-122G>A rs57764234 0.10014
NM_001170629.2(CHD8):c.5391-116C>T rs61973167 0.09511
NM_001170629.2(CHD8):c.2730+327A>G rs61973170 0.07637
NM_001170629.2(CHD8):c.2731-285G>A rs7141803 0.07618
NM_001170629.2(CHD8):c.5051+73A>G rs61973169 0.06826
NM_001170629.2(CHD8):c.7182+162G>T rs575071320 0.04973
NM_001170629.2(CHD8):c.2365-68A>T rs11851628 0.04366
NM_001170629.2(CHD8):c.2908-234A>G rs74352743 0.04229
NM_001170629.2(CHD8):c.2364+322A>G rs77637570 0.03690
NM_001170629.2(CHD8):c.1968+253A>G rs61973175 0.03677
NM_001170629.2(CHD8):c.4063-36A>G rs199499304 0.03652
NM_001170629.2(CHD8):c.2226+105G>A rs116179240 0.03645
NM_001170629.2(CHD8):c.5007A>G (p.Ala1669=) rs61752837 0.02585
NM_001170629.2(CHD8):c.1602-151C>G rs11848144 0.02440
NM_001170629.2(CHD8):c.2908-71T>C rs73579663 0.02429
NM_001170629.2(CHD8):c.2364+236C>T rs8015439 0.01915
NM_001170629.2(CHD8):c.3715-85G>T rs80311097 0.01760
NM_001170629.2(CHD8):c.2227-182A>G rs114842481 0.01744
NM_001170629.2(CHD8):c.1601+243A>T rs141185930 0.01696
NM_001170629.2(CHD8):c.7665T>C (p.Asp2555=) rs61748933 0.01650
NM_001170629.2(CHD8):c.6537C>T (p.Ser2179=) rs61756312 0.01457
NM_001170629.2(CHD8):c.3307+86T>C rs116904182 0.01023
NM_001170629.2(CHD8):c.1716+80C>T rs79484978 0.00918
NM_001170629.2(CHD8):c.1437C>T (p.Asn479=) rs61744173 0.00897
NM_001170629.2(CHD8):c.2373G>A (p.Pro791=) rs61752838 0.00607
NM_001170629.2(CHD8):c.1843C>T (p.Pro615Ser) rs61744458 0.00579
NM_001170629.2(CHD8):c.4818-63T>A rs140676325 0.00543
NM_001170629.2(CHD8):c.5121T>C (p.Asp1707=) rs61729945 0.00441
NM_001170629.2(CHD8):c.27C>T (p.Phe9=) rs75191413 0.00436
NM_001170629.2(CHD8):c.4809G>A (p.Ala1603=) rs61736703 0.00383
NM_001170629.2(CHD8):c.1822A>G (p.Ile608Val) rs200056646 0.00371
NM_001170629.2(CHD8):c.145A>G (p.Met49Val) rs181830482 0.00300
NM_001170629.2(CHD8):c.6571T>C (p.Leu2191=) rs61741241 0.00297
NM_001170629.2(CHD8):c.5391-40T>C rs188442867 0.00262
NM_001170629.2(CHD8):c.456A>G (p.Pro152=) rs61752839 0.00255
NM_001170629.2(CHD8):c.262G>A (p.Glu88Lys) rs78640816 0.00245
NM_001170629.2(CHD8):c.2907+12A>T rs200189975 0.00186
NM_001170629.2(CHD8):c.4921+16T>A rs142564496 0.00185
NM_001170629.2(CHD8):c.4173+11T>C rs143716456 0.00160
NM_001170629.2(CHD8):c.5390+10A>T rs181227407 0.00133
NM_001170629.2(CHD8):c.2025-36A>G rs187044867 0.00125
NM_001170629.2(CHD8):c.6650G>A (p.Arg2217Gln) rs149307240 0.00125
NM_001170629.2(CHD8):c.4728-19C>T rs187327123 0.00111
NM_001170629.2(CHD8):c.2487-15A>G rs374458289 0.00104
NM_001170629.2(CHD8):c.871C>T (p.Leu291Phe) rs192989929 0.00101
NM_001170629.2(CHD8):c.4921+7A>G rs375587003 0.00100
NM_001170629.2(CHD8):c.341C>T (p.Thr114Met) rs111250264 0.00096
NM_001170629.2(CHD8):c.5195A>G (p.Gln1732Arg) rs201074234 0.00091
NM_001170629.2(CHD8):c.2362G>A (p.Val788Met) rs191366877 0.00088
NM_001170629.2(CHD8):c.4571-10C>A rs150205863 0.00088
NM_001170629.2(CHD8):c.7203G>A (p.Val2401=) rs181239271 0.00084
NM_001170629.2(CHD8):c.6207G>A (p.Ser2069=) rs370827611 0.00080
NM_001170629.2(CHD8):c.3715-15T>G rs369876599 0.00076
NM_001170629.2(CHD8):c.6243T>A (p.Ser2081=) rs201856289 0.00075
NM_001170629.2(CHD8):c.2142+35C>T rs191496918 0.00070
NM_001170629.2(CHD8):c.5051+19T>A rs138127807 0.00066
NM_001170629.2(CHD8):c.3882+6T>C rs373037739 0.00059
NM_001170629.2(CHD8):c.6085G>A (p.Glu2029Lys) rs145300090 0.00058
NM_001170629.2(CHD8):c.1407T>C (p.Ile469=) rs190978463 0.00057
NM_001170629.2(CHD8):c.7620C>T (p.Asp2540=) rs367905297 0.00052
NM_001170629.2(CHD8):c.6119A>G (p.Asp2040Gly) rs148494847 0.00048
NM_001170629.2(CHD8):c.1717-4A>G rs191933523 0.00043
NM_001170629.2(CHD8):c.5128-34C>T rs58514360 0.00043
NM_001170629.2(CHD8):c.7472T>C (p.Met2491Thr) rs551653039 0.00041
NM_001170629.2(CHD8):c.3714+4A>G rs191258109 0.00039
NM_001170629.2(CHD8):c.6054T>C (p.Ser2018=) rs61752836 0.00037
NM_001170629.2(CHD8):c.5402G>A (p.Arg1801His) rs201604061 0.00036
NM_001170629.2(CHD8):c.6312G>A (p.Glu2104=) rs118140634 0.00030
NM_001170629.2(CHD8):c.6232C>T (p.Leu2078=) rs188900504 0.00028
NM_001170629.2(CHD8):c.7431G>A (p.Met2477Ile) rs375405457 0.00024
NM_001170629.2(CHD8):c.1601+29C>T rs375282372 0.00022
NM_001170629.2(CHD8):c.2487-37C>T rs541093415 0.00022
NM_001170629.2(CHD8):c.4921+5G>A rs377595194 0.00020
NM_001170629.2(CHD8):c.1325G>A (p.Gly442Glu) rs553367989 0.00019
NM_001170629.2(CHD8):c.1716+36C>A rs143279762 0.00016
NM_001170629.2(CHD8):c.2907+45C>T rs138832292 0.00013
NM_001170629.2(CHD8):c.5607C>T (p.Pro1869=) rs537080482 0.00009
NM_001170629.2(CHD8):c.1809T>C (p.Asp603=) rs755210469 0.00006
NM_001170629.2(CHD8):c.3396C>T (p.Ala1132=) rs200180762 0.00002
NM_001170629.2(CHD8):c.852G>A (p.Ser284=) rs765203840 0.00002
NM_001170629.2(CHD8):c.1216-21G>A rs377451081 0.00001
NM_001170629.2(CHD8):c.7253G>A (p.Arg2418Gln) rs573063062 0.00001
NM_001170629.2(CHD8):c.*142del rs370612022
NM_001170629.2(CHD8):c.1323G>A (p.Gly441=)
NM_001170629.2(CHD8):c.1395A>G (p.Val465=)
NM_001170629.2(CHD8):c.1494C>T (p.Gly498=)
NM_001170629.2(CHD8):c.1573T>C (p.Ser525Pro) rs771409666
NM_001170629.2(CHD8):c.1968+32ATTT[10] rs34695967
NM_001170629.2(CHD8):c.1968+32ATTT[7] rs34695967
NM_001170629.2(CHD8):c.2025-72C>A rs17792659
NM_001170629.2(CHD8):c.2226+16A>G
NM_001170629.2(CHD8):c.2487-28_2487-27dup rs111776414
NM_001170629.2(CHD8):c.2487-28dup rs111776414
NM_001170629.2(CHD8):c.2487-56dup rs145389674
NM_001170629.2(CHD8):c.2748C>T (p.Gly916=)
NM_001170629.2(CHD8):c.2763C>T (p.Asp921=)
NM_001170629.2(CHD8):c.2908-168_2908-167del rs141397644
NM_001170629.2(CHD8):c.2934A>G (p.Thr978=)
NM_001170629.2(CHD8):c.3051+24A>C rs150422713
NM_001170629.2(CHD8):c.3345T>C (p.Ala1115=)
NM_001170629.2(CHD8):c.3519-14C>T
NM_001170629.2(CHD8):c.3672C>T (p.Cys1224=)
NM_001170629.2(CHD8):c.4063-43dup rs113076568
NM_001170629.2(CHD8):c.4218C>T (p.Arg1406=)
NM_001170629.2(CHD8):c.4605A>G (p.Gly1535=)
NM_001170629.2(CHD8):c.4817+111A>G rs56229026
NM_001170629.2(CHD8):c.4922-19A>G
NM_001170629.2(CHD8):c.6168G>A (p.Arg2056=)
NM_001170629.2(CHD8):c.6468+117dup rs10646956
NM_001170629.2(CHD8):c.7182+163dup rs34364818
NM_001170629.2(CHD8):c.7182+177_7182+178del rs34364818
NM_001170629.2(CHD8):c.844-148G>T rs373148160

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.