Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.176093497delCA430224592HOXD13c.607del (p.Val203CysfsTer?)
c.725-983del (n.725-983del)
COSMIC
2g.176093497G>ACA349353098HOXD13c.607G>A (p.Val203Met)
c.725-983G>A (n.725-983G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.176093497G>CCA349353099HOXD13c.607G>C (p.Val203Leu)
c.725-983G>C (n.725-983G>C)
dbSNP gnomAD v4
2g.176093497G=CA1309431460HOXD13c.607G= (p.Val203=)
c.725-983G= (n.725-983G=)
2g.176093497G>TCA349353100HOXD13c.607G>T (p.Val203Leu)
c.725-983G>T (n.725-983G>T)
2g.176093498T>ACA349353101HOXD13c.608T>A (p.Val203Glu)
c.725-982T>A (n.725-982T>A)
dbSNP
2g.176093498T>CCA349353102HOXD13c.608T>C (p.Val203Ala)
c.725-982T>C (n.725-982T>C)
2g.176093498T>GCA349353103HOXD13c.608T>G (p.Val203Gly)
c.725-982T>G (n.725-982T>G)
2g.176093499G>ACA430224593HOXD13c.609G>A (p.Val203=)
c.725-981G>A (n.725-981G>A)
dbSNP
2g.176093499G>CCA430224594HOXD13c.609G>C (p.Val203=)
c.725-981G>C (n.725-981G>C)
dbSNP
2g.176093499G=CA1309431461HOXD13c.609G= (p.Val203=)
c.725-981G= (n.725-981G=)
2g.176093499G>TCA430224595HOXD13c.609G>T (p.Val203=)
c.725-981G>T (n.725-981G>T)
dbSNP gnomAD v2
2g.176093500C>ACA349353104HOXD13c.610C>A (p.Pro204Thr)
c.725-980C>A (n.725-980C>A)
dbSNP
2g.176093500C=CA1309431462HOXD13c.610C= (p.Pro204=)
c.725-980C= (n.725-980C=)
2g.176093500C>GCA349353105HOXD13c.610C>G (p.Pro204Ala)
c.725-980C>G (n.725-980C>G)
dbSNP gnomAD v3 gnomAD v4
2g.176093500C>TCA60846486HOXD13c.610C>T (p.Pro204Ser)
c.725-980C>T (n.725-980C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093502delCA2586965142HOXD13c.612del (p.Gly205AlafsTer?)
c.725-978del (n.725-978del)
2g.176093501C>ACA349353106HOXD13c.611C>A (p.Pro204His)
c.725-979C>A (n.725-979C>A)
gnomAD v4
2g.176093501C>GCA349353108HOXD13c.611C>G (p.Pro204Arg)
c.725-979C>G (n.725-979C>G)
dbSNP
2g.176093501C>TCA349353107HOXD13c.611C>T (p.Pro204Leu)
c.725-979C>T (n.725-979C>T)
COSMIC COSMIC
2g.176093502C>ACA430224596HOXD13c.612C>A (p.Pro204=)
c.725-978C>A (n.725-978C>A)
COSMIC COSMIC
2g.176093502C>GCA430224597HOXD13c.612C>G (p.Pro204=)
c.725-978C>G (n.725-978C>G)
2g.176093502C>TCA430224598HOXD13c.612C>T (p.Pro204=)
c.725-978C>T (n.725-978C>T)
gnomAD v4
2g.176093503G>ACA1976637HOXD13c.613G>A (p.Gly205Ser)
c.725-977G>A (n.725-977G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093503G>CCA349353109HOXD13c.613G>C (p.Gly205Arg)
c.725-977G>C (n.725-977G>C)
2g.176093503G=CA1309431463HOXD13c.613G= (p.Gly205=)
c.725-977G= (n.725-977G=)
2g.176093503G>TCA349353110HOXD13c.613G>T (p.Gly205Cys)
c.725-977G>T (n.725-977G>T)
2g.176093504G>ACA349353111HOXD13c.614G>A (p.Gly205Asp)
c.725-976G>A (n.725-976G>A)
dbSNP COSMIC COSMIC
2g.176093504G>CCA349353112HOXD13c.614G>C (p.Gly205Ala)
c.725-976G>C (n.725-976G>C)
dbSNP gnomAD v4
2g.176093504G>TCA349353113HOXD13c.614G>T (p.Gly205Val)
c.725-976G>T (n.725-976G>T)
2g.176093505C>ACA430224599HOXD13c.615C>A (p.Gly205=)
c.725-975C>A (n.725-975C>A)
2g.176093505C=CA1309431464HOXD13c.615C= (p.Gly205=)
c.725-975C= (n.725-975C=)
2g.176093505C>GCA430224600HOXD13c.615C>G (p.Gly205=)
c.725-975C>G (n.725-975C>G)
2g.176093505C>TCA60846502HOXD13c.615C>T (p.Gly205=)
c.725-975C>T (n.725-975C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093506T>ACA349353114HOXD13c.616T>A (p.Tyr206Asn)
c.725-974T>A (n.725-974T>A)
dbSNP
2g.176093506T>CCA349353115HOXD13c.616T>C (p.Tyr206His)
c.725-974T>C (n.725-974T>C)
2g.176093506T>GCA349353116HOXD13c.616T>G (p.Tyr206Asp)
c.725-974T>G (n.725-974T>G)
2g.176093507A=CA1309431465HOXD13c.617A= (p.Tyr206=)
c.725-973A= (n.725-973A=)
2g.176093507A>CCA349353118HOXD13c.617A>C (p.Tyr206Ser)
c.725-973A>C (n.725-973A>C)
2g.176093507A>GCA1976638HOXD13c.617A>G (p.Tyr206Cys)
c.725-973A>G (n.725-973A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093507A>TCA349353117HOXD13c.617A>T (p.Tyr206Phe)
c.725-973A>T (n.725-973A>T)
dbSNP
2g.176093508T>ACA349353119HOXD13c.618T>A (p.Tyr206Ter)
c.725-972T>A (n.725-972T>A)
dbSNP
2g.176093508T>CCA430224601HOXD13c.618T>C (p.Tyr206=)
c.725-972T>C (n.725-972T>C)
2g.176093508T>GCA349353120HOXD13c.618T>G (p.Tyr206Ter)
c.725-972T>G (n.725-972T>G)
2g.176093509A=CA1309431466HOXD13c.619A= (p.Ile207=)
c.725-971A= (n.725-971A=)
2g.176093509A>CCA349353121HOXD13c.619A>C (p.Ile207Leu)
c.725-971A>C (n.725-971A>C)
dbSNP
2g.176093509A>GCA1976639HOXD13c.619A>G (p.Ile207Val)
c.725-971A>G (n.725-971A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093509A>TCA349353122HOXD13c.619A>T (p.Ile207Phe)
c.725-971A>T (n.725-971A>T)
dbSNP
2g.176093510T>ACA349353123HOXD13c.620T>A (p.Ile207Asn)
c.725-970T>A (n.725-970T>A)
gnomAD v4
2g.176093510T>CCA349353124HOXD13c.620T>C (p.Ile207Thr)
c.725-970T>C (n.725-970T>C)
dbSNP gnomAD v4
2g.176093510T>GCA349353125HOXD13c.620T>G (p.Ile207Ser)
c.725-970T>G (n.725-970T>G)
2g.176093511C>ACA430224602HOXD13c.621C>A (p.Ile207=)
c.725-969C>A (n.725-969C>A)
dbSNP
2g.176093511C>GCA349353126HOXD13c.621C>G (p.Ile207Met)
c.725-969C>G (n.725-969C>G)
dbSNP
2g.176093511C>TCA430224603HOXD13c.621C>T (p.Ile207=)
c.725-969C>T (n.725-969C>T)
dbSNP gnomAD v4
2g.176093512G>ACA349353127HOXD13c.622G>A (p.Asp208Asn)
c.725-968G>A (n.725-968G>A)
dbSNP COSMIC
2g.176093512G>CCA349353128HOXD13c.622G>C (p.Asp208His)
c.725-968G>C (n.725-968G>C)
dbSNP
2g.176093512G>TCA349353129HOXD13c.622G>T (p.Asp208Tyr)
c.725-968G>T (n.725-968G>T)
2g.176093513A>CCA349353131HOXD13c.623A>C (p.Asp208Ala)
c.725-967A>C (n.725-967A>C)
dbSNP
2g.176093513A>GCA349353132HOXD13c.623A>G (p.Asp208Gly)
c.725-967A>G (n.725-967A>G)
dbSNP
2g.176093513A>TCA349353130HOXD13c.623A>T (p.Asp208Val)
c.725-967A>T (n.725-967A>T)
ClinVar dbSNP
2g.176093514C>ACA349353133HOXD13c.624C>A (p.Asp208Glu)
c.725-966C>A (n.725-966C>A)
dbSNP
2g.176093514C>GCA349353134HOXD13c.624C>G (p.Asp208Glu)
c.725-966C>G (n.725-966C>G)
dbSNP
2g.176093514C>TCA430224604HOXD13c.624C>T (p.Asp208=)
c.725-966C>T (n.725-966C>T)
2g.176093515A=CA1309431467HOXD13c.625A= (p.Met209=)
c.725-965A= (n.725-965A=)
2g.176093515A>CCA349353135HOXD13c.625A>C (p.Met209Leu)
c.725-965A>C (n.725-965A>C)
dbSNP gnomAD v4
2g.176093515A>GCA1976640HOXD13c.625A>G (p.Met209Val)
c.725-965A>G (n.725-965A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093515A>TCA349353136HOXD13c.625A>T (p.Met209Leu)
c.725-965A>T (n.725-965A>T)
dbSNP
2g.176093515_176093518delinsATGGCA1309431468HOXD13c.625_628delinsATGG (p.Met209=)
c.725-965_725-962delinsATGG (n.725-965_725-962delinsATGG)
2g.176093516T>ACA349353139HOXD13c.626T>A (p.Met209Lys)
c.725-964T>A (n.725-964T>A)
dbSNP
2g.176093516T>CCA349353137HOXD13c.626T>C (p.Met209Thr)
c.725-964T>C (n.725-964T>C)
2g.176093516T>GCA349353138HOXD13c.626T>G (p.Met209Arg)
c.725-964T>G (n.725-964T>G)
2g.176093518_176093520delCA537975473HOXD13c.628_630del (p.Val210del)
c.725-962_725-960del (n.725-962_725-960del)
dbSNP gnomAD v2 gnomAD v4
2g.176093517G>ACA349353140HOXD13c.627G>A (p.Met209Ile)
c.725-963G>A (n.725-963G>A)
dbSNP gnomAD v2 gnomAD v4
2g.176093517G>CCA349353141HOXD13c.627G>C (p.Met209Ile)
c.725-963G>C (n.725-963G>C)
dbSNP
2g.176093517G=CA1309431469HOXD13c.627G= (p.Met209=)
c.725-963G= (n.725-963G=)
2g.176093517G>TCA349353142HOXD13c.627G>T (p.Met209Ile)
c.725-963G>T (n.725-963G>T)
2g.176093518G>ACA349353143HOXD13c.628G>A (p.Val210Met)
c.725-962G>A (n.725-962G>A)
2g.176093518G>CCA349353144HOXD13c.628G>C (p.Val210Leu)
c.725-962G>C (n.725-962G>C)
dbSNP
2g.176093518G>TCA349353145HOXD13c.628G>T (p.Val210Leu)
c.725-962G>T (n.725-962G>T)
2g.176093519T>ACA349353147HOXD13c.629T>A (p.Val210Glu)
c.725-961T>A (n.725-961T>A)
2g.176093519T>CCA60846528HOXD13c.629T>C (p.Val210Ala)
c.725-961T>C (n.725-961T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093519T>GCA349353146HOXD13c.629T>G (p.Val210Gly)
c.725-961T>G (n.725-961T>G)
2g.176093519T=CA1309431470HOXD13c.629T= (p.Val210=)
c.725-961T= (n.725-961T=)
2g.176093520G>ACA430224605HOXD13c.630G>A (p.Val210=)
c.725-960G>A (n.725-960G>A)
dbSNP
2g.176093520G>CCA430224606HOXD13c.630G>C (p.Val210=)
c.725-960G>C (n.725-960G>C)
dbSNP
2g.176093520G>TCA430224607HOXD13c.630G>T (p.Val210=)
c.725-960G>T (n.725-960G>T)
2g.176093521T>ACA349353149HOXD13c.631T>A (p.Ser211Thr)
c.725-959T>A (n.725-959T>A)
2g.176093521T>CCA349353148HOXD13c.631T>C (p.Ser211Pro)
c.725-959T>C (n.725-959T>C)
2g.176093521T>GCA349353150HOXD13c.631T>G (p.Ser211Ala)
c.725-959T>G (n.725-959T>G)
2g.176093522C>ACA349353151HOXD13c.632C>A (p.Ser211Tyr)
c.725-958C>A (n.725-958C>A)
2g.176093522C>GCA349353152HOXD13c.632C>G (p.Ser211Cys)
c.725-958C>G (n.725-958C>G)
gnomAD v4
2g.176093522C>TCA349353153HOXD13c.632C>T (p.Ser211Phe)
c.725-958C>T (n.725-958C>T)
2g.176093523delCA2701097024HOXD13c.633del (p.Thr212LeufsTer?)
c.725-957del (n.725-957del)
dbSNP
2g.176093523C>ACA430224608HOXD13c.633C>A (p.Ser211=)
c.725-957C>A (n.725-957C>A)
2g.176093523C=CA1309431471HOXD13c.633C= (p.Ser211=)
c.725-957C= (n.725-957C=)
2g.176093523C>GCA430224609HOXD13c.633C>G (p.Ser211=)
c.725-957C>G (n.725-957C>G)
2g.176093523C>TCA430224610HOXD13c.633C>T (p.Ser211=)
c.725-957C>T (n.725-957C>T)
dbSNP gnomAD v4
2g.176093523_176093524insGGGGCTATATCGCA2662046507HOXD13c.633_634insGGGGCTATATCG (p.Ser211_Thr212insGlyAlaIleSer)
c.725-957_725-956insGGGGCTATATCG (n.725-957_725-956insGGGGCTATATCG)
gnomAD v4
2g.176093524delCA2701097050HOXD13c.634del (p.Thr212LeufsTer?)
c.725-956del (n.725-956del)
dbSNP
2g.176093524A>CCA349353154HOXD13c.634A>C (p.Thr212Pro)
c.725-956A>C (n.725-956A>C)
dbSNP
2g.176093524A>GCA349353155HOXD13c.634A>G (p.Thr212Ala)
c.725-956A>G (n.725-956A>G)
dbSNP
2g.176093524A>TCA349353156HOXD13c.634A>T (p.Thr212Ser)
c.725-956A>T (n.725-956A>T)
dbSNP
2g.176093525C>ACA349353157HOXD13c.635C>A (p.Thr212Asn)
c.725-955C>A (n.725-955C>A)
2g.176093525C>GCA349353158HOXD13c.635C>G (p.Thr212Ser)
c.725-955C>G (n.725-955C>G)
2g.176093525C>TCA349353159HOXD13c.635C>T (p.Thr212Ile)
c.725-955C>T (n.725-955C>T)
2g.176093526T>ACA430224611HOXD13c.636T>A (p.Thr212=)
c.725-954T>A (n.725-954T>A)
2g.176093526T>CCA430224613HOXD13c.636T>C (p.Thr212=)
c.725-954T>C (n.725-954T>C)
2g.176093526T>GCA430224612HOXD13c.636T>G (p.Thr212=)
c.725-954T>G (n.725-954T>G)
2g.176093527T>ACA349353160HOXD13c.637T>A (p.Phe213Ile)
c.725-953T>A (n.725-953T>A)
dbSNP
2g.176093527T>CCA349353161HOXD13c.637T>C (p.Phe213Leu)
c.725-953T>C (n.725-953T>C)
dbSNP
2g.176093527T>GCA349353162HOXD13c.637T>G (p.Phe213Val)
c.725-953T>G (n.725-953T>G)
2g.176093528T>ACA349353164HOXD13c.638T>A (p.Phe213Tyr)
c.725-952T>A (n.725-952T>A)
gnomAD v4
2g.176093528T>CCA60846553HOXD13c.638T>C (p.Phe213Ser)
c.725-952T>C (n.725-952T>C)
dbSNP
2g.176093528T>GCA349353163HOXD13c.638T>G (p.Phe213Cys)
c.725-952T>G (n.725-952T>G)
2g.176093528T=CA1309431472HOXD13c.638T= (p.Phe213=)
c.725-952T= (n.725-952T=)
2g.176093529C>ACA349353165HOXD13c.639C>A (p.Phe213Leu)
c.725-951C>A (n.725-951C>A)
dbSNP
2g.176093529C>GCA349353166HOXD13c.639C>G (p.Phe213Leu)
c.725-951C>G (n.725-951C>G)
dbSNP gnomAD v4
2g.176093529C>TCA430224614HOXD13c.639C>T (p.Phe213=)
c.725-951C>T (n.725-951C>T)
dbSNP gnomAD v4 COSMIC
2g.176093531_176093551delCA2701097511HOXD13c.641_661del (p.Gly214_His220del)
c.725-949_725-929del (n.725-949_725-929del)
dbSNP
2g.176093530G>ACA349353167HOXD13c.640G>A (p.Gly214Ser)
c.725-950G>A (n.725-950G>A)
dbSNP
2g.176093530G>CCA349353168HOXD13c.640G>C (p.Gly214Arg)
c.725-950G>C (n.725-950G>C)
2g.176093530G=CA1309431473HOXD13c.640G= (p.Gly214=)
c.725-950G= (n.725-950G=)
2g.176093530G>TCA349353169HOXD13c.640G>T (p.Gly214Cys)
c.725-950G>T (n.725-950G>T)
2g.176093531G>ACA349353170HOXD13c.641G>A (p.Gly214Asp)
c.725-949G>A (n.725-949G>A)
dbSNP
2g.176093531G>CCA349353171HOXD13c.641G>C (p.Gly214Ala)
c.725-949G>C (n.725-949G>C)
2g.176093531G>TCA349353172HOXD13c.641G>T (p.Gly214Val)
c.725-949G>T (n.725-949G>T)
2g.176093532C>ACA430224615HOXD13c.642C>A (p.Gly214=)
c.725-948C>A (n.725-948C>A)
dbSNP
2g.176093532C=CA1309431474HOXD13c.642C= (p.Gly214=)
c.725-948C= (n.725-948C=)
2g.176093532C>GCA430224616HOXD13c.642C>G (p.Gly214=)
c.725-948C>G (n.725-948C>G)
dbSNP
2g.176093532C>TCA1976641HOXD13c.642C>T (p.Gly214=)
c.725-948C>T (n.725-948C>T)
dbSNP ExAC gnomAD v2
2g.176093533T>ACA349353173HOXD13c.643T>A (p.Ser215Thr)
c.725-947T>A (n.725-947T>A)
2g.176093533T>CCA349353174HOXD13c.643T>C (p.Ser215Pro)
c.725-947T>C (n.725-947T>C)
dbSNP
2g.176093533T>GCA349353175HOXD13c.643T>G (p.Ser215Ala)
c.725-947T>G (n.725-947T>G)
2g.176093534C>ACA349353178HOXD13c.644C>A (p.Ser215Tyr)
c.725-946C>A (n.725-946C>A)
2g.176093534C=CA1309431475HOXD13c.644C= (p.Ser215=)
c.725-946C= (n.725-946C=)
2g.176093534C>GCA349353177HOXD13c.644C>G (p.Ser215Cys)
c.725-946C>G (n.725-946C>G)
dbSNP
2g.176093534C>TCA349353176HOXD13c.644C>T (p.Ser215Phe)
c.725-946C>T (n.725-946C>T)
dbSNP gnomAD v3 gnomAD v4
2g.176093535C>ACA430224619HOXD13c.645C>A (p.Ser215=)
c.725-945C>A (n.725-945C>A)
2g.176093535C>GCA430224618HOXD13c.645C>G (p.Ser215=)
c.725-945C>G (n.725-945C>G)
2g.176093535C>TCA430224617HOXD13c.645C>T (p.Ser215=)
c.725-945C>T (n.725-945C>T)
2g.176093536G>ACA349353179HOXD13c.646G>A (p.Gly216Arg)
c.725-944G>A (n.725-944G>A)
gnomAD v4
2g.176093536G>CCA349353180HOXD13c.646G>C (p.Gly216Arg)
c.725-944G>C (n.725-944G>C)
2g.176093536G>TCA349353181HOXD13c.646G>T (p.Gly216Trp)
c.725-944G>T (n.725-944G>T)
gnomAD v4
2g.176093537G>ACA349353182HOXD13c.647G>A (p.Gly216Glu)
c.725-943G>A (n.725-943G>A)
2g.176093537G>CCA349353183HOXD13c.647G>C (p.Gly216Ala)
c.725-943G>C (n.725-943G>C)
2g.176093537G>TCA349353184HOXD13c.647G>T (p.Gly216Val)
c.725-943G>T (n.725-943G>T)
2g.176093538G>ACA430224620HOXD13c.648G>A (p.Gly216=)
c.725-942G>A (n.725-942G>A)
dbSNP gnomAD v4
2g.176093538G>CCA430224621HOXD13c.648G>C (p.Gly216=)
c.725-942G>C (n.725-942G>C)
dbSNP
2g.176093538G=CA1309431476HOXD13c.648G= (p.Gly216=)
c.725-942G= (n.725-942G=)
2g.176093538G>TCA430224622HOXD13c.648G>T (p.Gly216=)
c.725-942G>T (n.725-942G>T)
dbSNP gnomAD v2 gnomAD v4
2g.176093539G>ACA349353187HOXD13c.649G>A (p.Glu217Lys)
c.725-941G>A (n.725-941G>A)
dbSNP COSMIC COSMIC
2g.176093539G>CCA349353185HOXD13c.649G>C (p.Glu217Gln)
c.725-941G>C (n.725-941G>C)
2g.176093539G=CA1309431477HOXD13c.649G= (p.Glu217=)
c.725-941G= (n.725-941G=)
2g.176093539G>TCA349353186HOXD13c.649G>T (p.Glu217Ter)
c.725-941G>T (n.725-941G>T)
2g.176093540A>CCA349353188HOXD13c.650A>C (p.Glu217Ala)
c.725-940A>C (n.725-940A>C)
2g.176093540A>GCA349353189HOXD13c.650A>G (p.Glu217Gly)
c.725-940A>G (n.725-940A>G)
dbSNP
2g.176093540A>TCA349353190HOXD13c.650A>T (p.Glu217Val)
c.725-940A>T (n.725-940A>T)
2g.176093541G>ACA430224623HOXD13c.651G>A (p.Glu217=)
c.725-939G>A (n.725-939G>A)
dbSNP gnomAD v4
2g.176093541G>CCA349353191HOXD13c.651G>C (p.Glu217Asp)
c.725-939G>C (n.725-939G>C)
dbSNP gnomAD v2
2g.176093541G=CA1309431478HOXD13c.651G= (p.Glu217=)
c.725-939G= (n.725-939G=)
2g.176093541G>TCA349353192HOXD13c.651G>T (p.Glu217Asp)
c.725-939G>T (n.725-939G>T)
2g.176093542C>ACA349353193HOXD13c.652C>A (p.Pro218Thr)
c.725-938C>A (n.725-938C>A)
2g.176093542C=CA1309431479HOXD13c.652C= (p.Pro218=)
c.725-938C= (n.725-938C=)
2g.176093542C>GCA349353195HOXD13c.652C>G (p.Pro218Ala)
c.725-938C>G (n.725-938C>G)
2g.176093542C>TCA349353194HOXD13c.652C>T (p.Pro218Ser)
c.725-938C>T (n.725-938C>T)
dbSNP
2g.176093543delCA2577165630HOXD13c.653del (p.Pro218LeufsTer?)
c.725-937del (n.725-937del)
2g.176093543C>ACA349353196HOXD13c.653C>A (p.Pro218His)
c.725-937C>A (n.725-937C>A)
dbSNP
2g.176093543C>GCA349353197HOXD13c.653C>G (p.Pro218Arg)
c.725-937C>G (n.725-937C>G)
2g.176093543C>TCA349353198HOXD13c.653C>T (p.Pro218Leu)
c.725-937C>T (n.725-937C>T)
dbSNP gnomAD v4
2g.176093544T>ACA430224624HOXD13c.654T>A (p.Pro218=)
c.725-936T>A (n.725-936T>A)
2g.176093544T>CCA430224625HOXD13c.654T>C (p.Pro218=)
c.725-936T>C (n.725-936T>C)
2g.176093544T>GCA430224626HOXD13c.654T>G (p.Pro218=)
c.725-936T>G (n.725-936T>G)
2g.176093545C>ACA430224627HOXD13c.655C>A (p.Arg219=)
c.725-935C>A (n.725-935C>A)
2g.176093545C=CA1309431480HOXD13c.655C= (p.Arg219=)
c.725-935C= (n.725-935C=)
2g.176093545C>GCA349353199HOXD13c.655C>G (p.Arg219Gly)
c.725-935C>G (n.725-935C>G)
2g.176093545C>TCA349353200HOXD13c.655C>T (p.Arg219Trp)
c.725-935C>T (n.725-935C>T)
dbSNP
2g.176093546G>ACA349353201HOXD13c.656G>A (p.Arg219Gln)
c.725-934G>A (n.725-934G>A)
gnomAD v4 COSMIC
2g.176093546G>CCA349353202HOXD13c.656G>C (p.Arg219Pro)
c.725-934G>C (n.725-934G>C)
gnomAD v4
2g.176093546G>TCA349353203HOXD13c.656G>T (p.Arg219Leu)
c.725-934G>T (n.725-934G>T)
2g.176093547G>ACA430224628HOXD13c.657G>A (p.Arg219=)
c.725-933G>A (n.725-933G>A)
dbSNP gnomAD v4
2g.176093547G>CCA430224629HOXD13c.657G>C (p.Arg219=)
c.725-933G>C (n.725-933G>C)
gnomAD v4
2g.176093547G>TCA430224630HOXD13c.657G>T (p.Arg219=)
c.725-933G>T (n.725-933G>T)
2g.176093548C>ACA349353204HOXD13c.658C>A (p.His220Asn)
c.725-932C>A (n.725-932C>A)
2g.176093548C>GCA349353205HOXD13c.658C>G (p.His220Asp)
c.725-932C>G (n.725-932C>G)
2g.176093548C>TCA349353206HOXD13c.658C>T (p.His220Tyr)
c.725-932C>T (n.725-932C>T)
gnomAD v4
2g.176093549A>CCA349353209HOXD13c.659A>C (p.His220Pro)
c.725-931A>C (n.725-931A>C)
2g.176093549A>GCA349353208HOXD13c.659A>G (p.His220Arg)
c.725-931A>G (n.725-931A>G)
2g.176093549A>TCA349353207HOXD13c.659A>T (p.His220Leu)
c.725-931A>T (n.725-931A>T)
2g.176093550C>ACA349353210HOXD13c.660C>A (p.His220Gln)
c.725-930C>A (n.725-930C>A)
2g.176093550C>GCA349353211HOXD13c.660C>G (p.His220Gln)
c.725-930C>G (n.725-930C>G)
gnomAD v4
2g.176093550C>TCA430224631HOXD13c.660C>T (p.His220=)
c.725-930C>T (n.725-930C>T)
2g.176093551G>ACA349353212HOXD13c.661G>A (p.Glu221Lys)
c.725-929G>A (n.725-929G>A)
dbSNP gnomAD v4 COSMIC
2g.176093551G>CCA349353213HOXD13c.661G>C (p.Glu221Gln)
c.725-929G>C (n.725-929G>C)
2g.176093551G=CA1309431481HOXD13c.661G= (p.Glu221=)
c.725-929G= (n.725-929G=)
2g.176093551G>TCA349353214HOXD13c.661G>T (p.Glu221Ter)
c.725-929G>T (n.725-929G>T)
2g.176093552A>CCA349353215HOXD13c.662A>C (p.Glu221Ala)
c.725-928A>C (n.725-928A>C)
2g.176093552A>GCA349353216HOXD13c.662A>G (p.Glu221Gly)
c.725-928A>G (n.725-928A>G)
2g.176093552A>TCA349353217HOXD13c.662A>T (p.Glu221Val)
c.725-928A>T (n.725-928A>T)
2g.176093553G>ACA430224632HOXD13c.663G>A (p.Glu221=)
c.725-927G>A (n.725-927G>A)
dbSNP gnomAD v4
2g.176093553G>CCA349353219HOXD13c.663G>C (p.Glu221Asp)
c.725-927G>C (n.725-927G>C)
2g.176093553G=CA1309431482HOXD13c.663G= (p.Glu221=)
c.725-927G= (n.725-927G=)
2g.176093553G>TCA349353218HOXD13c.663G>T (p.Glu221Asp)
c.725-927G>T (n.725-927G>T)
COSMIC
2g.176093554G>ACA349353220HOXD13c.664G>A (p.Ala222Thr)
c.725-926G>A (n.725-926G>A)
dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
2g.176093554G>CCA349353221HOXD13c.664G>C (p.Ala222Pro)
c.725-926G>C (n.725-926G>C)
2g.176093554G=CA1309431483HOXD13c.664G= (p.Ala222=)
c.725-926G= (n.725-926G=)
2g.176093554G>TCA349353222HOXD13c.664G>T (p.Ala222Ser)
c.725-926G>T (n.725-926G>T)
2g.176093555C>ACA349353223HOXD13c.665C>A (p.Ala222Asp)
c.725-925C>A (n.725-925C>A)
2g.176093555C>GCA349353224HOXD13c.665C>G (p.Ala222Gly)
c.725-925C>G (n.725-925C>G)
2g.176093555C>TCA349353225HOXD13c.665C>T (p.Ala222Val)
c.725-925C>T (n.725-925C>T)
gnomAD v4
2g.176093556C>ACA430224633HOXD13c.666C>A (p.Ala222=)
c.725-924C>A (n.725-924C>A)
2g.176093556C>GCA430224635HOXD13c.666C>G (p.Ala222=)
c.725-924C>G (n.725-924C>G)
2g.176093556C>TCA430224634HOXD13c.666C>T (p.Ala222=)
c.725-924C>T (n.725-924C>T)
2g.176093557T>ACA349353226HOXD13c.667T>A (p.Tyr223Asn)
c.725-923T>A (n.725-923T>A)
2g.176093557T>CCA349353228HOXD13c.667T>C (p.Tyr223His)
c.725-923T>C (n.725-923T>C)
2g.176093557T>GCA349353227HOXD13c.667T>G (p.Tyr223Asp)
c.725-923T>G (n.725-923T>G)
2g.176093558A=CA1309431484HOXD13c.668A= (p.Tyr223=)
c.725-922A= (n.725-922A=)
2g.176093558A>CCA349353229HOXD13c.668A>C (p.Tyr223Ser)
c.725-922A>C (n.725-922A>C)
gnomAD v4
2g.176093558A>GCA349353230HOXD13c.668A>G (p.Tyr223Cys)
c.725-922A>G (n.725-922A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093558A>TCA349353231HOXD13c.668A>T (p.Tyr223Phe)
c.725-922A>T (n.725-922A>T)
2g.176093559C>ACA349353232HOXD13c.669C>A (p.Tyr223Ter)
c.725-921C>A (n.725-921C>A)
2g.176093559C>GCA349353233HOXD13c.669C>G (p.Tyr223Ter)
c.725-921C>G (n.725-921C>G)
2g.176093559C>TCA430224636HOXD13c.669C>T (p.Tyr223=)
c.725-921C>T (n.725-921C>T)
2g.176093560A=CA1309431485HOXD13c.670A= (p.Ile224=)
c.725-920A= (n.725-920A=)
2g.176093560A>CCA349353234HOXD13c.670A>C (p.Ile224Leu)
c.725-920A>C (n.725-920A>C)
2g.176093560A>GCA1976642HOXD13c.670A>G (p.Ile224Val)
c.725-920A>G (n.725-920A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093560A>TCA349353235HOXD13c.670A>T (p.Ile224Phe)
c.725-920A>T (n.725-920A>T)
2g.176093561T>ACA349353236HOXD13c.671T>A (p.Ile224Asn)
c.725-919T>A (n.725-919T>A)
2g.176093561T>CCA349353237HOXD13c.671T>C (p.Ile224Thr)
c.725-919T>C (n.725-919T>C)
2g.176093561T>GCA349353238HOXD13c.671T>G (p.Ile224Ser)
c.725-919T>G (n.725-919T>G)
2g.176093562C>ACA430224637HOXD13c.672C>A (p.Ile224=)
c.725-918C>A (n.725-918C>A)
2g.176093562C>GCA349353239HOXD13c.672C>G (p.Ile224Met)
c.725-918C>G (n.725-918C>G)
dbSNP
2g.176093562C>TCA430224638HOXD13c.672C>T (p.Ile224=)
c.725-918C>T (n.725-918C>T)
2g.176093563T>ACA349353242HOXD13c.673T>A (p.Ser225Thr)
c.725-917T>A (n.725-917T>A)
2g.176093563T>CCA349353240HOXD13c.673T>C (p.Ser225Pro)
c.725-917T>C (n.725-917T>C)
2g.176093563T>GCA349353241HOXD13c.673T>G (p.Ser225Ala)
c.725-917T>G (n.725-917T>G)
2g.176093564C>ACA349353243HOXD13c.674C>A (p.Ser225Tyr)
c.725-916C>A (n.725-916C>A)
2g.176093564C=CA1309431486HOXD13c.674C= (p.Ser225=)
c.725-916C= (n.725-916C=)
2g.176093564C>GCA60846579HOXD13c.674C>G (p.Ser225Cys)
c.725-916C>G (n.725-916C>G)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.176093564C>TCA349353244HOXD13c.674C>T (p.Ser225Phe)
c.725-916C>T (n.725-916C>T)
2g.176093565C>ACA430224639HOXD13c.675C>A (p.Ser225=)
c.725-915C>A (n.725-915C>A)
2g.176093565C>GCA430224640HOXD13c.675C>G (p.Ser225=)
c.725-915C>G (n.725-915C>G)
2g.176093565C>TCA430224641HOXD13c.675C>T (p.Ser225=)
c.725-915C>T (n.725-915C>T)
2g.176093565_176093566insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACGCA430224642HOXD13c.675_676insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG (p.Met226AlafsTer34)
c.725-915_725-914insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG (n.725-915_725-914insGCGGCCGAACCGAGCCTTGGATGGCGTCATTCCCCCCGATTGGTGGCGATGACGCCGCGACTTGAGGGGGTGTGGCCGCCAAAGTGCAGCCCCATTGGGTGAAAACAGTCAAATGACG)
2g.176093566A>CCA349353247HOXD13c.676A>C (p.Met226Leu)
c.725-914A>C (n.725-914A>C)
2g.176093566A>GCA349353246HOXD13c.676A>G (p.Met226Val)
c.725-914A>G (n.725-914A>G)
gnomAD v4 COSMIC
2g.176093566A>TCA349353245HOXD13c.676A>T (p.Met226Leu)
c.725-914A>T (n.725-914A>T)
2g.176093567T>ACA349353248HOXD13c.677T>A (p.Met226Lys)
c.725-913T>A (n.725-913T>A)
2g.176093567T>CCA349353249HOXD13c.677T>C (p.Met226Thr)
c.725-913T>C (n.725-913T>C)
dbSNP gnomAD v3 gnomAD v4
2g.176093567T>GCA349353250HOXD13c.677T>G (p.Met226Arg)
c.725-913T>G (n.725-913T>G)
2g.176093567T=CA1309431487HOXD13c.677T= (p.Met226=)
c.725-913T= (n.725-913T=)
2g.176093568G>ACA349353251HOXD13c.678G>A (p.Met226Ile)
c.725-912G>A (n.725-912G>A)
dbSNP
2g.176093568G>CCA349353252HOXD13c.678G>C (p.Met226Ile)
c.725-912G>C (n.725-912G>C)
2g.176093568G=CA1309431488HOXD13c.678G= (p.Met226=)
c.725-912G= (n.725-912G=)
2g.176093568G>TCA349353253HOXD13c.678G>T (p.Met226Ile)
c.725-912G>T (n.725-912G>T)
2g.176093569G>ACA349353254HOXD13c.679G>A (p.Glu227Lys)
c.725-911G>A (n.725-911G>A)
2g.176093569G>CCA349353256HOXD13c.679G>C (p.Glu227Gln)
c.725-911G>C (n.725-911G>C)
2g.176093569G>TCA349353255HOXD13c.679G>T (p.Glu227Ter)
c.725-911G>T (n.725-911G>T)
2g.176093570A>CCA349353257HOXD13c.680A>C (p.Glu227Ala)
c.725-910A>C (n.725-910A>C)
2g.176093570A>GCA349353258HOXD13c.680A>G (p.Glu227Gly)
c.725-910A>G (n.725-910A>G)
2g.176093570A>TCA349353259HOXD13c.680A>T (p.Glu227Val)
c.725-910A>T (n.725-910A>T)
2g.176093571G>ACA429991657HOXD13c.681G>A (p.Glu227=)
c.725-909G>A (n.725-909G>A)
dbSNP gnomAD v3 gnomAD v4 COSMIC
2g.176093571G>CCA349353260HOXD13c.681G>C (p.Glu227Asp)
c.725-909G>C (n.725-909G>C)
2g.176093571G=CA1309431489HOXD13c.681G= (p.Glu227=)
c.725-909G= (n.725-909G=)
2g.176093571G>TCA349353261HOXD13c.681G>T (p.Glu227Asp)
c.725-909G>T (n.725-909G>T)
gnomAD v4
2g.176093574dupCA2580614418HOXD13c.684dup (p.Tyr229ValfsTer8)
c.725-906dup (n.725-906dup)
ClinVar
2g.176093572G>ACA349353262HOXD13c.682G>A (p.Gly228Arg)
c.725-908G>A (n.725-908G>A)
2g.176093572G>CCA349353263HOXD13c.682G>C (p.Gly228Arg)
c.725-908G>C (n.725-908G>C)
dbSNP
2g.176093572G=CA1309431490HOXD13c.682G= (p.Gly228=)
c.725-908G= (n.725-908G=)
2g.176093572G>TCA349353264HOXD13c.682G>T (p.Gly228Trp)
c.725-908G>T (n.725-908G>T)
2g.176093573G>ACA349353265HOXD13c.683G>A (p.Gly228Glu)
c.725-907G>A (n.725-907G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093573G>CCA16040613HOXD13c.683G>C (p.Gly228Ala)
c.725-907G>C (n.725-907G>C)
ClinVar dbSNP
2g.176093573G=CA1309431491HOXD13c.683G= (p.Gly228=)
c.725-907G= (n.725-907G=)
2g.176093573G>TCA124419HOXD13c.683G>T (p.Gly228Val)
c.725-907G>T (n.725-907G>T)
ClinVar dbSNP
2g.176093574G>ACA429991668HOXD13c.684G>A (p.Gly228=)
c.725-906G>A (n.725-906G>A)
gnomAD v4
2g.176093574G>CCA429991670HOXD13c.684G>C (p.Gly228=)
c.725-906G>C (n.725-906G>C)
2g.176093574G>TCA429991672HOXD13c.684G>T (p.Gly228=)
c.725-906G>T (n.725-906G>T)
2g.176093575T>ACA349353268HOXD13c.685T>A (p.Tyr229Asn)
c.725-905T>A (n.725-905T>A)
2g.176093575T>CCA349353267HOXD13c.685T>C (p.Tyr229His)
c.725-905T>C (n.725-905T>C)
2g.176093575T>GCA349353266HOXD13c.685T>G (p.Tyr229Asp)
c.725-905T>G (n.725-905T>G)
dbSNP
2g.176093575T=CA1309431492HOXD13c.685T= (p.Tyr229=)
c.725-905T= (n.725-905T=)
2g.176093576A=CA1309431493HOXD13c.686A= (p.Tyr229=)
c.725-904A= (n.725-904A=)
2g.176093576A>CCA349353269HOXD13c.686A>C (p.Tyr229Ser)
c.725-904A>C (n.725-904A>C)
2g.176093576A>GCA1976643HOXD13c.686A>G (p.Tyr229Cys)
c.725-904A>G (n.725-904A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093576A>TCA349353270HOXD13c.686A>T (p.Tyr229Phe)
c.725-904A>T (n.725-904A>T)
2g.176093577C>ACA349353271HOXD13c.687C>A (p.Tyr229Ter)
c.725-903C>A (n.725-903C>A)
2g.176093577C>GCA349353272HOXD13c.687C>G (p.Tyr229Ter)
c.725-903C>G (n.725-903C>G)
2g.176093577C>TCA429991680HOXD13c.687C>T (p.Tyr229=)
c.725-903C>T (n.725-903C>T)
gnomAD v4
2g.176093578C>ACA349353273HOXD13c.688C>A (p.Gln230Lys)
c.725-902C>A (n.725-902C>A)
2g.176093578C>GCA349353274HOXD13c.688C>G (p.Gln230Glu)
c.725-902C>G (n.725-902C>G)
2g.176093578C>TCA349353275HOXD13c.688C>T (p.Gln230Ter)
c.725-902C>T (n.725-902C>T)
2g.176093579A=CA1309431494HOXD13c.689A= (p.Gln230=)
c.725-901A= (n.725-901A=)
2g.176093579A>CCA349353276HOXD13c.689A>C (p.Gln230Pro)
c.725-901A>C (n.725-901A>C)
2g.176093579A>GCA349353278HOXD13c.689A>G (p.Gln230Arg)
c.725-901A>G (n.725-901A>G)
dbSNP gnomAD v4
2g.176093579A>TCA349353277HOXD13c.689A>T (p.Gln230Leu)
c.725-901A>T (n.725-901A>T)
2g.176093580G>ACA429991690HOXD13c.690G>A (p.Gln230=)
c.725-900G>A (n.725-900G>A)
2g.176093580G>CCA1976644HOXD13c.690G>C (p.Gln230His)
c.725-900G>C (n.725-900G>C)
dbSNP ExAC gnomAD v2
2g.176093580G=CA1309431495HOXD13c.690G= (p.Gln230=)
c.725-900G= (n.725-900G=)
2g.176093580G>TCA349353279HOXD13c.690G>T (p.Gln230His)
c.725-900G>T (n.725-900G>T)
2g.176093580_176093583delCA913089434HOXD13c.690_693del (p.Gln230HisfsTer?)
c.725-900_725-897del (n.725-900_725-897del)
2g.176093581T>ACA349353280HOXD13c.691T>A (p.Ser231Thr)
c.725-899T>A (n.725-899T>A)
2g.176093581T>CCA349353281HOXD13c.691T>C (p.Ser231Pro)
c.725-899T>C (n.725-899T>C)
2g.176093581T>GCA349353282HOXD13c.691T>G (p.Ser231Ala)
c.725-899T>G (n.725-899T>G)
2g.176093582C>ACA349353283HOXD13c.692C>A (p.Ser231Tyr)
c.725-898C>A (n.725-898C>A)
2g.176093582C>GCA349353285HOXD13c.692C>G (p.Ser231Cys)
c.725-898C>G (n.725-898C>G)
2g.176093582C>TCA349353284HOXD13c.692C>T (p.Ser231Phe)
c.725-898C>T (n.725-898C>T)
2g.176093583C>ACA429991701HOXD13c.693C>A (p.Ser231=)
c.725-897C>A (n.725-897C>A)
2g.176093583C>GCA429991703HOXD13c.693C>G (p.Ser231=)
c.725-897C>G (n.725-897C>G)
2g.176093583C>TCA429991705HOXD13c.693C>T (p.Ser231=)
c.725-897C>T (n.725-897C>T)
2g.176093584T>ACA349353286HOXD13c.694T>A (p.Trp232Arg)
c.725-896T>A (n.725-896T>A)
2g.176093584T>CCA349353287HOXD13c.694T>C (p.Trp232Arg)
c.725-896T>C (n.725-896T>C)
gnomAD v4
2g.176093584T>GCA349353288HOXD13c.694T>G (p.Trp232Gly)
c.725-896T>G (n.725-896T>G)
2g.176093585G>ACA349353289HOXD13c.695G>A (p.Trp232Ter)
c.725-895G>A (n.725-895G>A)
2g.176093585G>CCA349353290HOXD13c.695G>C (p.Trp232Ser)
c.725-895G>C (n.725-895G>C)
2g.176093585G>TCA349353291HOXD13c.695G>T (p.Trp232Leu)
c.725-895G>T (n.725-895G>T)
2g.176093586G>ACA349353292HOXD13c.696G>A (p.Trp232Ter)
c.725-894G>A (n.725-894G>A)
gnomAD v4
2g.176093586G>CCA349353293HOXD13c.696G>C (p.Trp232Cys)
c.725-894G>C (n.725-894G>C)
2g.176093586G>TCA349353294HOXD13c.696G>T (p.Trp232Cys)
c.725-894G>T (n.725-894G>T)
2g.176093587A>CCA349353295HOXD13c.697A>C (p.Thr233Pro)
c.725-893A>C (n.725-893A>C)
2g.176093587A>GCA349353296HOXD13c.697A>G (p.Thr233Ala)
c.725-893A>G (n.725-893A>G)
2g.176093587A>TCA349353297HOXD13c.697A>T (p.Thr233Ser)
c.725-893A>T (n.725-893A>T)
2g.176093588C>ACA349353300HOXD13c.698C>A (p.Thr233Lys)
c.725-892C>A (n.725-892C>A)
2g.176093588C=CA1309431496HOXD13c.698C= (p.Thr233=)
c.725-892C= (n.725-892C=)
2g.176093588C>GCA349353298HOXD13c.698C>G (p.Thr233Arg)
c.725-892C>G (n.725-892C>G)
dbSNP
2g.176093588C>TCA349353299HOXD13c.698C>T (p.Thr233Met)
c.725-892C>T (n.725-892C>T)
gnomAD v4
2g.176093589G>ACA429991724HOXD13c.699G>A (p.Thr233=)
c.725-891G>A (n.725-891G>A)
2g.176093589G>CCA429991725HOXD13c.699G>C (p.Thr233=)
c.725-891G>C (n.725-891G>C)
2g.176093589G>TCA429991727HOXD13c.699G>T (p.Thr233=)
c.725-891G>T (n.725-891G>T)
gnomAD v4
2g.176093590C>ACA349353301HOXD13c.700C>A (p.Leu234Met)
c.725-890C>A (n.725-890C>A)
2g.176093590C=CA1309431497HOXD13c.700C= (p.Leu234=)
c.725-890C= (n.725-890C=)
2g.176093590C>GCA349353302HOXD13c.700C>G (p.Leu234Val)
c.725-890C>G (n.725-890C>G)
2g.176093590C>TCA429991730HOXD13c.700C>T (p.Leu234=)
c.725-890C>T (n.725-890C>T)
dbSNP gnomAD v2 gnomAD v4
2g.176093591T>ACA349353303HOXD13c.701T>A (p.Leu234Gln)
c.725-889T>A (n.725-889T>A)
2g.176093591T>CCA349353304HOXD13c.701T>C (p.Leu234Pro)
c.725-889T>C (n.725-889T>C)
gnomAD v4
2g.176093591T>GCA349353305HOXD13c.701T>G (p.Leu234Arg)
c.725-889T>G (n.725-889T>G)
2g.176093592G>ACA429991733HOXD13c.702G>A (p.Leu234=)
c.725-888G>A (n.725-888G>A)
gnomAD v4
2g.176093592G>CCA429991734HOXD13c.702G>C (p.Leu234=)
c.725-888G>C (n.725-888G>C)
2g.176093592G>TCA429991737HOXD13c.702G>T (p.Leu234=)
c.725-888G>T (n.725-888G>T)
2g.176093593G>ACA349353308HOXD13c.703G>A (p.Ala235Thr)
c.725-887G>A (n.725-887G>A)
2g.176093593G>CCA349353307HOXD13c.703G>C (p.Ala235Pro)
c.725-887G>C (n.725-887G>C)
2g.176093593G>TCA349353306HOXD13c.703G>T (p.Ala235Ser)
c.725-887G>T (n.725-887G>T)
2g.176093594C>ACA349353309HOXD13c.704C>A (p.Ala235Asp)
c.725-886C>A (n.725-886C>A)
2g.176093594C>GCA349353310HOXD13c.704C>G (p.Ala235Gly)
c.725-886C>G (n.725-886C>G)
gnomAD v4
2g.176093594C>TCA349353311HOXD13c.704C>T (p.Ala235Val)
c.725-886C>T (n.725-886C>T)
2g.176093595T>ACA429991743HOXD13c.705T>A (p.Ala235=)
c.725-885T>A (n.725-885T>A)
2g.176093595T>CCA429991745HOXD13c.705T>C (p.Ala235=)
c.725-885T>C (n.725-885T>C)
2g.176093595T>GCA429991747HOXD13c.705T>G (p.Ala235=)
c.725-885T>G (n.725-885T>G)
2g.176093596A>CCA349353312HOXD13c.706A>C (p.Asn236His)
c.725-884A>C (n.725-884A>C)
2g.176093596A>GCA349353313HOXD13c.706A>G (p.Asn236Asp)
c.725-884A>G (n.725-884A>G)
2g.176093596A>TCA349353314HOXD13c.706A>T (p.Asn236Tyr)
c.725-884A>T (n.725-884A>T)
2g.176093597A>CCA349353317HOXD13c.707A>C (p.Asn236Thr)
c.725-883A>C (n.725-883A>C)
2g.176093597A>GCA349353315HOXD13c.707A>G (p.Asn236Ser)
c.725-883A>G (n.725-883A>G)
2g.176093597A>TCA349353316HOXD13c.707A>T (p.Asn236Ile)
c.725-883A>T (n.725-883A>T)

Number of alleles fetched