Colorectal Cancer Atlas

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All With sequence variants Without sequence variants

3 prime UTR variant (48366)

5 prime UTR variant (7065)

5 prime flank (18)

Coding silent variant (105464)

Complex (141)

Compound substitution (6)

De novo start in frame variant (24)

De novo start out of frame variant (170)

Deletion (70820)

Dinucleotide polymorphism (283)

Downstream variant (1107)

Frame shift (30487)

Frame shift deletion (3615)

Frame shift insertion (1640)

In frame deletion (420)

In frame insertion (150)

In-frame deletion (3648)

In-frame insertion (156)

Insertion (33155)

Intronic variant (38220)

Missense (339471)

Nonframeshift deletion (685)

Nonframeshit insertion (483)

Nonsense mutation (26103)

Nonstop extension (219)

Nonstop variant (47)

Nonsynonymous (112836)

RNA variant (72)

Silent (19488)

Single Nucleotide Variation (131662)

Splice site (2430)

Splice site DNP (2)

Splice site deletion (104)

Splice site insertion (271)

Stop codon insertion (6)

Stop gain (1949)

Stop gain SNV (26)

Stop loss (98)

Stop loss SNV (1)

Substitution (581532)

Synonymous (63313)

Translation start site (2)

Trinucleotide polymorphism (1)

Unknown sequence_variants (4897)

Unknown mutation effects (5142)

Upstream variant (1067)

Upstream;downstream (5)

ncRNA UTR3 variant (771)

ncRNA UTR5 variant (97)

ncRNA exonic variant (6109)

ncRNA intronic variant (1576)

Confocal microscopy

FACS

Immunoelectron microscopy

Immunohistochemistry

Mass spectrometry

Western blotting

Genes

Sequence variants

Cell lines

Techniques

Tissues

Compare gene sequence variants in cell lines