view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CSTF3_chr11_33079584_33166480 | 33163899 | ATATATAT others(21): Show |
A | upstream_gene_variant | MODIFIER | HG02723.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | 324 | 0.0123 | -28 | c.-26 others(39): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 2420 | chr11 | TogoVar | |||||||
CSTF3_chr11_33079584_33166480 | 33163901 | ATATATAT others(21): Show |
A | upstream_gene_variant | MODIFIER | HG02630.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0210 others(2): Show |
5 | 303 | 0.0165 | -28 | c.-26 others(39): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 2422 | chr11 | TogoVar | |||||||
CSTF3_chr11_33079584_33166480 | 33163903 | ATATATAT others(21): Show |
A | upstream_gene_variant | MODIFIER | HG02486.hp2 HG03486.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203 a0001c0001t0001g0215 a0001c0001t0001g0224 |
3 | 334 | 0.0090 | -28 | c.-26 others(39): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 2424 | chr11 | TogoVar | |||||||
CSTF3_chr11_33079584_33166480 | 33163905 | ATATATAT others(21): Show |
A | upstream_gene_variant | MODIFIER | HG03195.hp2 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | 348 | 0.0057 | -28 | c.-26 others(39): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 2426 | chr11 | TogoVar | |||||||
CSTPP1_chr11_46931761_47167247 | 47124064 | TATTGAGA others(21): Show |
T | intron_variant | MODIFIER | NA18992.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 | 1 | 222 | 0.0045 | -28 | c.281 others(47): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CT45A1_chrX_135708639_135728228 | 135715335 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG02257.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0019 | 1 | 43 | 0.0233 | -28 | c.-7+ others(43): Show |
CT45A1 | ENSG00000268940.6 | transcript | ENST00000594565.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79741018 | GGTCCCCC others(21): Show |
G | intron_variant | MODIFIER | NA18944.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0144 | 1 | 376 | 0.0027 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745246 | ATGCGCGT others(21): Show |
A | intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0037 | a0001c0037t0001 | a0001c0037t0001g0082 | 1 | 337 | 0.0030 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745315 | CCCTGCGT others(21): Show |
C | intron_variant | MODIFIER | HG01255.hp2 HG01934.hp1 HG02109.hp1 others(3): Show |
a0001a0008a0011 | a0001c0001a0001c0007a0001c0018others(2): Show | a0001c0001t0001a0001c0007t0003a0001c0018t0001others(2): Show | a0001c0001t0001g0087 a0001c0007t0003g0346 a0001c0018t0001g0089 others(3): Show |
6 | 376 | 0.0160 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745318 | TGCGTCCC others(21): Show |
T | intron_variant | MODIFIER | HG02040.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0302 | 1 | 267 | 0.0037 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745371 | GCCCGCGT others(21): Show |
G | intron_variant | MODIFIER | HG01106.hp2 HG01361.hp1 HG02258.hp1 others(2): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0042others(2): Show | a0001c0001t0002a0001c0003t0001a0001c0042t0001others(2): Show | a0001c0001t0002g0186 a0001c0003t0001g0077 a0001c0042t0001g0099 others(2): Show |
5 | 260 | 0.0192 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745503 | CGTTCTGT others(21): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(56): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0017a0001c0021others(7): Show | a0001c0001t0002a0001c0017t0003a0001c0021t0007others(7): Show | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0153 others(54): Show |
59 | 339 | 0.1740 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745567 | CCCCGCGT others(21): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG01167.hp2 HG03130.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0017a0001c0008t0001a0002c0002t0001 | a0001c0001t0017g0206 a0001c0008t0001g0204 a0002c0002t0001g0214 others(2): Show |
5 | 286 | 0.0175 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745567 | CCCCGCGT others(21): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(52): Show |
a0001a0002a0006others(3): Show | a0001c0001a0002c0002a0006c0010others(3): Show | a0001c0001t0002a0002c0002t0001a0006c0010t0001others(3): Show | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0153 others(50): Show |
55 | 336 | 0.1637 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | chr18 | TogoVar | |||||||
CTDP1_chr18_79674803_79759503 | 79745839 | CGTTCTGT others(21): Show |
C | intron_variant | MODIFIER | HG01516.hp1 HG01517.hp1 HG01981.hp2 others(9): Show |
a0002a0004a0005others(1): Show | a0002c0002a0004c0004a0005c0015others(2): Show | a0002c0002t0001a0004c0004t0001a0005c0015t0005others(2): Show | a0002c0002t0001g0210 a0002c0002t0001g0211 a0002c0002t0001g0213 others(9): Show |
12 | 299 | 0.0401 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745867 | GGTTCTGT others(21): Show |
G | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0018 | a0001c0018t0001 | a0001c0018t0001g0090 | 1 | 246 | 0.0041 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79745903 | CCCCGCGT others(21): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0007others(7): Show | a0001c0001t0002a0001c0001t0017a0001c0003t0001others(8): Show | a0001c0001t0002g0005 a0001c0001t0002g0022 a0001c0001t0002g0023 others(93): Show |
100 | 274 | 0.3650 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79746071 | GCCCGCGT others(21): Show |
C | intron_variant | MODIFIER | HG02280.hp2 HG03453.hp2 HG03491.hp1 others(6): Show |
a0001a0004 | a0001c0001a0001c0014a0001c0018others(1): Show | a0001c0001t0002a0001c0014t0001a0001c0018t0001others(1): Show | a0001c0001t0002g0025 a0001c0001t0002g0163 a0001c0001t0002g0165 others(6): Show |
9 | 325 | 0.0277 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | chr18 | TogoVar | |||||||
CTDP1_chr18_79674803_79759503 | 79746071 | GCCCGCGT others(21): Show |
G | intron_variant | MODIFIER | HG03579.hp2 NA19030.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0041 | a0001c0001t0008a0001c0041t0013 | a0001c0001t0008g0102 a0001c0001t0008g0105 a0001c0041t0013g0100 |
3 | 319 | 0.0094 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79746175 | CGTTCTGT others(21): Show |
C | intron_variant | MODIFIER | HG01952.hp2 HG02040.hp1 |
a0001a0004 | a0001c0008a0004c0004 | a0001c0008t0001a0004c0004t0001 | a0001c0008t0001g0198 a0004c0004t0001g0302 |
2 | 362 | 0.0055 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79746210 | TCCCCGCG others(21): Show |
T | intron_variant | MODIFIER | HG00735.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0214 | 1 | 361 | 0.0028 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79746298 | TGCGTCCC others(21): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0003a0001c0007others(14): Show | a0001c0001t0002a0001c0003t0001a0001c0003t0002others(17): Show | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0150 others(98): Show |
103 | 295 | 0.3492 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTDP1_chr18_79674803_79759503 | 79746338 | GTGCGCGT others(21): Show |
G | intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0101 | 1 | 376 | 0.0027 | -28 | c.274 others(47): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTIF_chr18_48534031_48868217 | 48669793 | TTATATAT others(21): Show |
T | intron_variant | MODIFIER | HG02896.hp1 HG03098.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0039a0001c0001t0046 | a0001c0001t0008g0007 a0001c0001t0039g0043 a0001c0001t0046g0031 |
3 | 38 | 0.0789 | -28 | c.432 others(43): Show |
CTIF | ENSG00000134030.14 | transcript | ENST00000256413.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
CTLA4_chr2_203862771_203878965 | 203873327 | CATATATA others(21): Show |
C | 3_prime_UTR_variant | MODIFIER | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0017a0002c0002t0017 | a0001c0003t0017g0002 a0002c0002t0017g0001 |
6 | 27 | 0.2222 | -28 | c.*54 others(37): Show |
CTLA4 | ENSG00000163599.18 | transcript | ENST00000648405.2 | protein_coding | 4/4 | 544 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CTNNA2_chr2_79508051_80653780 | 79508955 | GTATATAT others(21): Show |
G | upstream_gene_variant | MODIFIER | HG03139.hp1 HG03225.hp1 |
a0001a0002 | a0001c0002a0002c0008 | a0001c0002t0001a0002c0008t0001 | a0001c0002t0001g0004 a0002c0008t0001g0002 |
2 | 7 | 0.2857 | -28 | c.-42 others(39): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 4095 | chr2 | TogoVar | |||||||
CTNNA2_chr2_79508051_80653780 | 79521107 | GATATATA others(21): Show |
G | intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0005 | 1 | 11 | 0.0909 | -28 | c.-6+ others(43): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 79930274 | GAAAGAGA others(21): Show |
G | intron_variant | MODIFIER | HG02148.hp1 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0010 a0001c0001t0002g0041 |
2 | 67 | 0.0299 | -28 | c.105 others(49): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 79930294 | GAGAAAGA others(21): Show |
G | intron_variant | MODIFIER | HG03209.hp2 HG03516.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0003t0001 | a0001c0002t0002g0025 a0001c0003t0001g0005 |
2 | 32 | 0.0625 | -28 | c.105 others(49): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 79982192 | CTATATAT others(21): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG02148.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0016 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0010 a0001c0002t0001g0037 a0001c0002t0001g0047 others(2): Show |
5 | 23 | 0.2174 | -28 | c.105 others(49): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 80043073 | TTCTTTCT others(21): Show |
T | intron_variant | MODIFIER | HG03471.hp2 HG03927.hp2 |
a0001a0002 | a0001c0003a0002c0006 | a0001c0003t0001a0002c0006t0001 | a0001c0003t0001g0018 a0002c0006t0001g0060 |
2 | 66 | 0.0303 | -28 | c.105 others(51): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 80043115 | CTTTCTCC others(21): Show |
C | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0025 | 1 | 59 | 0.0169 | -28 | c.105 others(51): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 80043119 | CTCCTTCC others(21): Show |
C | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055 | 1 | 55 | 0.0182 | -28 | c.105 others(51): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 80043157 | CCTTCCTT others(21): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG01106.hp2 HG02148.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0002t0001g0047 others(1): Show |
4 | 68 | 0.0588 | -28 | c.105 others(51): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA2_chr2_79508051_80653780 | 80126584 | TTCCCTCC others(21): Show |
T | intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0036 | 1 | 17 | 0.0588 | -28 | c.105 others(51): Show |
CTNNA2 | ENSG00000066032.19 | transcript | ENST00000402739.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CTNNA3_chr10_65907523_67701195 | 66346232 | TATATATA others(21): Show |
T | intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024 | 1 | 37 | 0.0270 | -28 | c.173 others(49): Show |
CTNNA3 | ENSG00000183230.18 | transcript | ENST00000433211.7 | protein_coding | 12/17 | chr10 | TogoVar | |||||||
CTNNA3_chr10_65907523_67701195 | 66360634 | TCTTTCTT others(21): Show |
T | intron_variant | MODIFIER | HG06807.hp1 | a0005 | a0005c0008 | a0005c0008t0005 | a0005c0008t0005g0033 | 1 | 46 | 0.0217 | -28 | c.173 others(49): Show |
CTNNA3 | ENSG00000183230.18 | transcript | ENST00000433211.7 | protein_coding | 12/17 | chr10 | TogoVar | |||||||
CTNNA3_chr10_65907523_67701195 | 66360804 | CCTTCCTT others(21): Show |
C | intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0019 | 1 | 40 | 0.0250 | -28 | c.173 others(49): Show |
CTNNA3 | ENSG00000183230.18 | transcript | ENST00000433211.7 | protein_coding | 12/17 | chr10 | TogoVar | |||||||
CTNNA3_chr10_65907523_67701195 | 66360901 | CTCTCTCT others(21): Show |
C | intron_variant | MODIFIER | HG02145.hp2 | a0003 | a0003c0009 | a0003c0009t0003 | a0003c0009t0003g0036 | 1 | 46 | 0.0217 | -28 | c.173 others(49): Show |
CTNNA3 | ENSG00000183230.18 | transcript | ENST00000433211.7 | protein_coding | 12/17 | chr10 | TogoVar | |||||||
CTNNA3_chr10_65907523_67701195 | 66966482 | TATATTTT others(21): Show |
T | intron_variant | MODIFIER | NA18612.hp2 NA19080.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0002 | a0001c0001t0004g0043 a0002c0002t0002g0013 |
2 | 46 | 0.0435 | -28 | c.104 others(51): Show |
CTNNA3 | ENSG00000183230.18 | transcript | ENST00000433211.7 | protein_coding | 7/17 | chr10 | TogoVar | |||||||
CTNNA3_chr10_65907523_67701195 | 67302002 | CGAAAGAA others(21): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG02622.hp1 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0023 | a0001c0001t0002g0010 a0001c0001t0007g0020 a0001c0001t0023g0012 |
3 | 30 | 0.1000 | -28 | c.580 others(47): Show |
CTNNA3 | ENSG00000183230.18 | transcript | ENST00000433211.7 | protein_coding | 5/17 | chr10 | TogoVar | |||||||
CTNND2_chr5_10966836_11909446 | 11623789 | AATATATA others(21): Show |
A | intron_variant | MODIFIER | NA19068.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 23 | 0.0435 | -28 | c.175 others(47): Show |
CTNND2 | ENSG00000169862.21 | transcript | ENST00000304623.13 | protein_coding | 2/21 | chr5 | TogoVar | |||||||
CTNND2_chr5_10966836_11909446 | 11817410 | GGAGAGAG others(21): Show |
G | intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 | 1 | 7 | 0.1429 | -28 | c.38- others(45): Show |
CTNND2 | ENSG00000169862.21 | transcript | ENST00000304623.13 | protein_coding | 1/21 | chr5 | TogoVar | |||||||
CTSC_chr11_88288592_88342736 | 88290844 | CATATATA others(21): Show |
C | downstream_gene_variant | MODIFIER | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | 28 | 0.1071 | -28 | c.*31 others(39): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2747 | chr11 | TogoVar | |||||||
CUL3_chr2_224465150_224590363 | 224535001 | AAAATAAA others(21): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0159 a0001c0001t0002g0168 |
2 | 47 | 0.0426 | -28 | c.378 others(43): Show |
CUL3 | ENSG00000036257.14 | transcript | ENST00000264414.9 | protein_coding | 3/15 | chr2 | TogoVar | |||||||
CUL7_chr6_43032617_43058851 | 43039151 | CTCTGGGC others(21): Show |
C | intron_variant | MODIFIER | NA19076.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0142 | 1 | 300 | 0.0033 | -28 | c.429 others(45): Show |
CUL7 | ENSG00000044090.13 | transcript | ENST00000265348.9 | protein_coding | 22/25 | chr6 | TogoVar | |||||||
CUX1_chr7_101811007_102288958 | 101939058 | CATATATA others(21): Show |
C | intron_variant | MODIFIER | HG02572.hp2 HG02615.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0002t0001g0079 |
3 | 14 | 0.2143 | -28 | c.174 others(47): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 101984122 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG01978.hp1 HG02056.hp2 HG02300.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0032 others(8): Show |
11 | 130 | 0.0846 | -28 | c.175 others(47): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 101939058 | CATATATA others(21): Show |
C | intron_variant | MODIFIER | HG02572.hp1 HG02615.hp1 NA19043.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0012a0001c0003t0004 | a0001c0002t0012g0045 a0001c0003t0004g0029 a0001c0003t0004g0032 |
3 | 14 | 0.2143 | -28 | c.141 others(47): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 101984122 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG01978.hp1 HG02056.hp2 HG02300.hp1 others(8): Show |
a0001a0002 | a0001c0003a0001c0004a0001c0009others(1): Show | a0001c0003t0009a0001c0003t0035a0001c0004t0007others(7): Show | a0001c0003t0009g0102 a0001c0003t0035g0114 a0001c0004t0007g0131 others(8): Show |
11 | 134 | 0.0821 | -28 | c.142 others(47): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |