Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.3256646A>GCA11632806MSANTD1c.729+789A>G (p.=)
n.753+789A>G
c.765+753A>G (p.=)
dbSNP gnomAD
4g.3256648_3256650delCA794017915MSANTD1c.729+791_729+793del (p.=)
n.753+791_753+793del
c.765+755_765+757del (p.=)
4g.3256649A>GCA91448510MSANTD1c.729+792A>G (p.=)
n.753+792A>G
c.765+756A>G (p.=)
dbSNP
4g.3256655G>CCA91448526MSANTD1c.729+798G>C (p.=)
n.753+798G>C
c.765+762G>C (p.=)
dbSNP gnomAD
4g.3256664A>GCA91448531MSANTD1c.729+807A>G (p.=)
n.753+807A>G
c.765+771A>G (p.=)
dbSNP gnomAD
4g.3256688T>CCA549307486MSANTD1c.729+831T>C (p.=)
n.753+831T>C
c.765+795T>C (p.=)
gnomAD
4g.3256692C>GCA91448532MSANTD1c.729+835C>G (p.=)
n.753+835C>G
c.765+799C>G (p.=)
dbSNP
4g.3256696T>GCA794017925MSANTD1c.729+839T>G (p.=)
n.753+839T>G
c.765+803T>G (p.=)
4g.3256698C>TCA794017931MSANTD1c.729+841C>T (p.=)
n.753+841C>T
c.765+805C>T (p.=)
4g.3256702delCA91448537MSANTD1c.729+845del (p.=)
n.753+845del
c.765+809del (p.=)
dbSNP gnomAD
4g.3256702G>TCA91448545MSANTD1c.729+845G>T (p.=)
n.753+845G>T
c.765+809G>T (p.=)
dbSNP
4g.3256704A>GCA91448553MSANTD1c.729+847A>G (p.=)
n.753+847A>G
c.765+811A>G (p.=)
dbSNP gnomAD
4g.3256713G>CCA91448555MSANTD1c.729+856G>C (p.=)
n.753+856G>C
c.765+820G>C (p.=)
dbSNP gnomAD
4g.3256714G>TCA91448559MSANTD1c.729+857G>T (p.=)
n.753+857G>T
c.765+821G>T (p.=)
dbSNP
4g.3256720A>GCA91448563MSANTD1c.729+863A>G (p.=)
n.753+863A>G
c.765+827A>G (p.=)
dbSNP
4g.3256723G>ACA91448566MSANTD1c.729+866G>A (p.=)
n.753+866G>A
c.765+830G>A (p.=)
dbSNP
4g.3256727T>CCA91448570MSANTD1c.729+870T>C (p.=)
n.753+870T>C
c.765+834T>C (p.=)
dbSNP
4g.3256729G>ACA794017942MSANTD1c.729+872G>A (p.=)
n.753+872G>A
c.765+836G>A (p.=)
4g.3256730T>CCA794017946MSANTD1c.729+873T>C (p.=)
n.753+873T>C
c.765+837T>C (p.=)
4g.3256736G>ACA91448584MSANTD1c.729+879G>A (p.=)
n.753+879G>A
c.765+843G>A (p.=)
dbSNP
4g.3256739delCA794017949MSANTD1c.729+882del (p.=)
n.753+882del
c.765+846del (p.=)
4g.3256740T>GCA794017954MSANTD1c.729+883T>G (p.=)
n.753+883T>G
c.765+847T>G (p.=)
4g.3256742A>GCA91448587MSANTD1c.729+885A>G (p.=)
n.753+885A>G
c.765+849A>G (p.=)
dbSNP
4g.3256745A>CCA794017956MSANTD1c.729+888A>C (p.=)
n.753+888A>C
c.765+852A>C (p.=)

Number of alleles fetched