DSCAML1 DS cell adhesion molecule like 1

Canonical transcript: NM_020693

45 unique variant annotations were identified in 43 publications

Variant ID cDot pDot Consequence Exon Intron Reference Count
11-117299039-G-A c.*5C>T - 3-UTRSNV 33/33 - 1
11-117299039-G-C c.*5C>G - 3-UTRSNV 33/33 - 1
11-117299039-G-T c.*5C>A - 3-UTRSNV 33/33 - 1
11-117299079-C-T c.6127G>A p.Ala2043Thr Missense 33/33 - 1
11-117301521-C-T c.5603G>A p.Arg1868His Missense 32/33 - 1
11-117303202-A-T c.5045T>A p.Ile1682Asn Missense 30/33 - 1
11-117306398-C-A c.4838G>T p.Arg1613Leu Missense 27/33 - 1
11-117308649-C-T c.4394G>A p.Arg1465His Missense 25/33 - 1
11-117319260-G-A c.3708+2005C>T - intron_variant - 20/32 1
11-117340673-C-T c.2977G>A p.Val993Ile Missense 16/33 - 1
11-117342607-A-C c.2930T>G p.Leu977Arg Missense 15/33 - 1
11-117342751-T-A c.2786A>T p.Asp929Val Missense 15/33 - 1
11-117350137-G-A c.2785+1021C>T - intron_variant - 14/32 1
11-117357140-A-G c.2360-4263T>C - intron_variant - 11/32 1
11-117388932-C-G c.1510+249G>C - intron_variant - 7/32 2
11-117388932-C-T c.1510+249G>A - intron_variant - 7/32 2
11-117389460-C-T c.1231G>A p.Val411Ile Missense 7/33 - 1
11-117392107-CAC-TTT c.949_951delinsAAA p.Val317Lys Missense 6/33 - 1
11-117395598-C-T c.859G>A p.Glu287Lys Missense 5/33 - 1
11-117395712-C-T c.745G>A p.Ala249Thr Missense 5/33 - 1
11-117407301-G-A c.512-4064C>T - intron_variant - 3/32 1
11-117421799-C-G c.512-18562G>C - intron_variant - 3/32 1
11-117421799-C-T c.512-18562G>A - intron_variant - 3/32 1
11-117459662-T-C c.512-56425A>G - intron_variant - 3/32 1
11-117461602-C-T c.512-58365G>A - intron_variant - 3/32 1
11-117475233-C-T c.512-71996G>A - intron_variant - 3/32 2
11-117510958-T-C c.512-107721A>G - intron_variant - 3/32 1
11-117521967-T-C c.512-118730A>G - intron_variant - 3/32 1
11-117521967-T-G c.512-118730A>C - intron_variant - 3/32 1
11-117524000-T-G c.512-120763A>C - intron_variant - 3/32 1
11-117525125-T-C c.512-121888A>G - intron_variant - 3/32 1
11-117529622-C-T c.511+117884G>A - intron_variant - 3/32 1
11-117531731-C-T c.511+115775G>A - intron_variant - 3/32 12
11-117532543-A-G c.511+114963T>C - intron_variant - 3/32 1
11-117534353-A-C c.511+113153T>G - intron_variant - 3/32 1
11-117534353-A-T c.511+113153T>A - intron_variant - 3/32 1
11-117546482-A-G c.511+101024T>C - intron_variant - 3/32 1
11-117623291-G-A c.511+24215C>T - intron_variant - 3/32 1
11-117643264-G-A c.511+4242C>T - intron_variant - 3/32 1
11-117643264-G-C c.511+4242C>G - intron_variant - 3/32 1
11-117651398-TC-AT c.173_174delinsAT p.Arg58His Missense 2/33 - 1
11-117657679-A-G c.47-6154T>C - intron_variant - 1/32 1
11-117660275-C-G c.46+7474G>C - intron_variant - 1/32 2
11-117660275-C-T c.46+7474G>A - intron_variant - 1/32 2
11-117662909-C-A c.46+4840G>T - intron_variant - 1/32 1