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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CLN8_chr8_1758789_1791570 | 1785248 | CCTACGGT others(38): Show |
C | 3_prime_UTR_variant | MODIFIER | HG01256.hp1 | a0001 | a0001c0001 | a0001c0001t0045 | a0001c0001t0045g0001 | 1 | 413 | 0.0024 | -45 | c.*47 others(56): Show |
CLN8 | ENSG00000182372.10 | transcript | ENST00000331222.6 | protein_coding | 3/3 | 4704 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CLN8_chr8_1758789_1791570 | 1785302 | ACACAGGC others(38): Show |
A | 3_prime_UTR_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0075 | a0001c0001t0075g0016 | 1 | 413 | 0.0024 | -45 | c.*47 others(56): Show |
CLN8 | ENSG00000182372.10 | transcript | ENST00000331222.6 | protein_coding | 3/3 | 4749 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CLN8_chr8_1758789_1791570 | 1785490 | GGCGTGGG others(38): Show |
G | 3_prime_UTR_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0085 | a0001c0001t0085g0131 | 1 | 413 | 0.0024 | -45 | c.*49 others(56): Show |
CLN8 | ENSG00000182372.10 | transcript | ENST00000331222.6 | protein_coding | 3/3 | 4968 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
CMC4_chrX_155056622_155076136 | 155057034 | CCTCATCC others(38): Show |
C | downstream_gene_variant | MODIFIER | HG00280.hp1 HG01168.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 2 | 292 | 0.0069 | -45 | c.*47 others(56): Show |
CMC4 | ENSG00000182712.16 | transcript | ENST00000369484.8 | protein_coding | 4587 | chrX | TogoVar | |||||||
CMKLR2_chr2_206170316_206218371 | 206172992 | AGGGAGAG others(38): Show |
A | downstream_gene_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0111 | 1 | 322 | 0.0031 | -45 | c.*31 others(56): Show |
CMKLR2 | ENSG00000183671.13 | transcript | ENST00000621141.5 | protein_coding | 2323 | chr2 | TogoVar | |||||||
CNTN1_chr12_40687439_41077415 | 41056912 | ATTTATAA others(38): Show |
A | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(18): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0005a0001c0002t0003others(8): Show | a0001c0001t0002g0131 a0001c0001t0005g0020 a0001c0001t0005g0135 others(18): Show |
21 | 230 | 0.0913 | -45 | c.298 others(66): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2287666 | AGAAGAAG others(38): Show |
A | intron_variant | MODIFIER | HG00738.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0001 | a0001c0001t0005g0054 a0001c0002t0001g0088 |
2 | 116 | 0.0172 | -45 | c.-14 others(66): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99598258 | CCTTTTCT others(38): Show |
C | intron_variant | MODIFIER | HG01496.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(7): Show | a0001c0001t0001g0008 a0001c0001t0004g0044 a0001c0001t0005g0048 others(7): Show |
10 | 66 | 0.1515 | -45 | c.55+ others(62): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147575139 | GTGTGTGT others(38): Show |
G | intron_variant | MODIFIER | HG02630.hp2 HG03239.hp1 |
a0001a0005 | a0001c0002a0005c0007 | a0001c0002t0002a0005c0007t0017 | a0001c0002t0002g0013 a0005c0007t0017g0031 |
2 | 40 | 0.0500 | -45 | c.189 others(66): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTROB_chr17_7927206_7954920 | 7934867 | GACTTTGG others(38): Show |
G | intron_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 402 | 0.0025 | -45 | c.438 others(59): Show |
CNTROB | ENSG00000170037.14 | transcript | ENST00000563694.6 | protein_coding | 3/18 | chr17 | TogoVar | |||||||
COL13A1_chr10_69796906_69964144 | 69936133 | GAAGGAAG others(38): Show |
G | intron_variant | MODIFIER | HG01081.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0151 | 1 | 324 | 0.0031 | -45 | c.177 others(62): Show |
COL13A1 | ENSG00000197467.17 | transcript | ENST00000645393.2 | protein_coding | 32/40 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
COL26A1_chr7_101357875_101564024 | 101539112 | GCCTCCCT others(38): Show |
G | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0002 | a0001c0002t0020 | a0001c0002t0020g0001 | 1 | 174 | 0.0058 | -45 | c.448 others(60): Show |
COL26A1 | ENSG00000160963.14 | transcript | ENST00000313669.12 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
COL3A1_chr2_188969373_189017746 | 188988663 | ATATTTAG others(38): Show |
A | intron_variant | MODIFIER | HG02165.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0087 | 1 | 376 | 0.0027 | -45 | c.636 others(58): Show |
COL3A1 | ENSG00000168542.17 | transcript | ENST00000304636.9 | protein_coding | 7/50 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110321208 | GTATATAT others(38): Show |
G | intron_variant | MODIFIER | HG02559.hp2 HG03471.hp1 HG03579.hp2 others(2): Show |
a0002a0003a0006 | a0002c0040a0002c0099a0003c0067others(2): Show | a0002c0040t0018a0002c0099t0001a0003c0067t0050others(2): Show | a0002c0040t0018g0003 a0002c0099t0001g0210 a0003c0067t0050g0151 others(2): Show |
5 | 372 | 0.0134 | -45 | c.99+ others(62): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 3/47 | chr13 | TogoVar | |||||||
COL5A1_chr9_134636803_134849843 | 134669212 | TTTCCCTT others(38): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG03098.hp2 HG03579.hp1 |
a0001 | a0001c0002a0001c0003a0001c0039 | a0001c0002t0042a0001c0003t0044a0001c0039t0035 | a0001c0002t0042g0185 a0001c0003t0044g0186 a0001c0039t0035g0045 |
3 | 272 | 0.0110 | -45 | c.110 others(64): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 1/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL6A1_chr21_45976770_46010048 | 45977812 | GAGGGAGG others(38): Show |
G | upstream_gene_variant | MODIFIER | HG02559.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
a0001a0002a0031others(1): Show | a0001c0032a0002c0001a0031c0049others(1): Show | a0001c0032t0007a0002c0001t0001a0002c0001t0008others(2): Show | a0001c0032t0007g0046 a0002c0001t0001g0043 a0002c0001t0008g0118 others(2): Show |
5 | 128 | 0.0391 | -45 | c.-40 others(56): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 3957 | chr21 | TogoVar | |||||||
COL6A1_chr21_45976770_46010048 | 45988141 | GTGGTCCA others(38): Show |
G | intron_variant | MODIFIER | HG02572.hp1 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0043 | 1 | 128 | 0.0078 | -45 | c.804 others(60): Show |
COL6A1 | ENSG00000142156.16 | transcript | ENST00000361866.8 | protein_coding | 8/34 | chr21 | TogoVar | |||||||
COMMD1_chr2_61900674_62141058 | 62109638 | TTCAGTCT others(38): Show |
T | intron_variant | MODIFIER | NA18946.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0120 | 1 | 286 | 0.0035 | -45 | c.463 others(64): Show |
COMMD1 | ENSG00000173163.11 | transcript | ENST00000311832.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COPS7B_chr2_231781445_231814253 | 231809588 | GCTATTCT others(38): Show |
G | downstream_gene_variant | MODIFIER | HG02523.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0046 | 1 | 348 | 0.0029 | -45 | c.*19 others(56): Show |
COPS7B | ENSG00000144524.18 | transcript | ENST00000350033.8 | protein_coding | 336 | chr2 | TogoVar | |||||||
CPA6_chr8_67417038_67751360 | 67607169 | CTCTTCTT others(38): Show |
C | intron_variant | MODIFIER | HG01891.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0013 | 1 | 144 | 0.0069 | -45 | c.192 others(64): Show |
CPA6 | ENSG00000165078.13 | transcript | ENST00000297770.10 | protein_coding | 2/10 | chr8 | TogoVar | |||||||
CPNE7_chr16_89570758_89602246 | 89580396 | ATCACCCG others(38): Show |
A | intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0061 | 1 | 348 | 0.0029 | -45 | c.357 others(62): Show |
CPNE7 | ENSG00000178773.15 | transcript | ENST00000319518.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CPSF1_chr8_144388231_144414335 | 144398163 | CCCCACCA others(38): Show |
C | intron_variant | MODIFIER | HG02976.hp2 HG03453.hp2 |
a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0157 a0001c0010t0001g0164 |
2 | 350 | 0.0057 | -45 | c.189 others(60): Show |
CPSF1 | ENSG00000071894.17 | transcript | ENST00000616140.2 | protein_coding | 19/37 | chr8 | TogoVar | |||||||
CRCP_chr7_66109847_66159568 | 66115475 | GCTGGTTT others(38): Show |
G | intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0022 | 1 | 380 | 0.0026 | -45 | c.8+5 others(56): Show |
CRCP | ENSG00000241258.7 | transcript | ENST00000395326.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CRLF2_chrX_1185490_1217649 | 1210142 | AAAAGAAA others(38): Show |
A | intron_variant | MODIFIER | HG01884.hp1 | a0010 | a0010c0018 | a0010c0018t0001 | a0010c0018t0001g0002 | 1 | 167 | 0.0060 | -45 | c.80- others(60): Show |
CRLF2 | ENSG00000205755.13 | transcript | ENST00000400841.8 | protein_coding | 1/7 | chrX | TogoVar | |||||||
CROCC2_chr2_240901336_240998311 | 240976489 | TCCCAGGC others(38): Show |
T | intron_variant | MODIFIER | NA21309.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0033 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240976646 | GCTCTGGG others(38): Show |
G | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(29): Show |
a0002a0007a0011others(5): Show | a0002c0001a0002c0022a0002c0070others(8): Show | a0002c0001t0001a0002c0001t0002a0002c0022t0002others(9): Show | a0002c0001t0001g0058 a0002c0001t0001g0082 a0002c0001t0001g0154 others(29): Show |
32 | 350 | 0.0914 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240976691 | TCTCTGGG others(38): Show |
T | intron_variant | MODIFIER | HG01943.hp2 | a0015 | a0015c0064 | a0015c0064t0002 | a0015c0064t0002g0307 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240976800 | AGGAGCCC others(38): Show |
A | intron_variant | MODIFIER | HG02970.hp2 NA18952.hp1 |
a0002a0045 | a0002c0001a0045c0028 | a0002c0001t0002a0045c0028t0003 | a0002c0001t0002g0311 a0045c0028t0003g0026 |
2 | 350 | 0.0057 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240976855 | GCTCATCC others(38): Show |
G | intron_variant | MODIFIER | HG00673.hp2 HG02027.hp1 HG02300.hp2 others(19): Show |
a0002a0005a0007others(5): Show | a0002c0001a0005c0005a0007c0006others(5): Show | a0002c0001t0002a0005c0005t0001a0005c0005t0002others(7): Show | a0002c0001t0002g0247 a0005c0005t0001g0016 a0005c0005t0001g0017 others(19): Show |
22 | 350 | 0.0629 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240976890 | AGGAGCCC others(38): Show |
A | intron_variant | MODIFIER | NA21309.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0033 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240976939 | GCCCAGGC others(38): Show |
G | intron_variant | MODIFIER | HG02622.hp1 HG02895.hp2 |
a0002 | a0002c0001 | a0002c0001t0003 | a0002c0001t0003g0144 a0002c0001t0003g0145 |
2 | 350 | 0.0057 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240977411 | TCTCTGGG others(38): Show |
T | intron_variant | MODIFIER | HG03710.hp1 NA18945.hp1 NA19002.hp2 |
a0002a0007a0009 | a0002c0001a0007c0006a0009c0010 | a0002c0001t0003a0007c0006t0003a0009c0010t0003 | a0002c0001t0003g0064 a0007c0006t0003g0002 a0009c0010t0003g0211 |
3 | 350 | 0.0086 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240977951 | TCTCTGGG others(38): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
a0002a0028 | a0002c0001a0028c0038 | a0002c0001t0003a0002c0001t0004a0028c0038t0003 | a0002c0001t0003g0003 a0002c0001t0003g0143 a0002c0001t0004g0303 others(2): Show |
6 | 350 | 0.0171 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240977996 | GCTCTGGG others(38): Show |
G | intron_variant | MODIFIER | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(11): Show |
a0002a0005a0011others(4): Show | a0002c0001a0005c0005a0011c0047others(4): Show | a0002c0001t0001a0002c0001t0002a0005c0005t0001others(6): Show | a0002c0001t0001g0154 a0002c0001t0002g0274 a0002c0001t0002g0277 others(11): Show |
14 | 350 | 0.0400 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978019 | TCCCAGGC others(38): Show |
T | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp1 HG01099.hp2 others(44): Show |
a0002a0005a0007others(9): Show | a0002c0001a0005c0005a0007c0006others(10): Show | a0002c0001t0002a0002c0001t0003a0002c0001t0004others(13): Show | a0002c0001t0002g0236 a0002c0001t0003g0064 a0002c0001t0003g0140 others(42): Show |
47 | 350 | 0.1343 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978260 | GCTCAGTC others(38): Show |
G | intron_variant | MODIFIER | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(11): Show |
a0002a0005a0011others(5): Show | a0002c0001a0005c0005a0011c0047others(5): Show | a0002c0001t0001a0002c0001t0002a0002c0001t0003others(8): Show | a0002c0001t0001g0154 a0002c0001t0002g0277 a0002c0001t0002g0308 others(11): Show |
14 | 350 | 0.0400 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978285 | AGGATCCC others(38): Show |
A | intron_variant | MODIFIER | NA18964.hp1 NA19004.hp1 NA19011.hp1 |
a0006a0010 | a0006c0007a0010c0009 | a0006c0007t0001a0010c0009t0001 | a0006c0007t0001g0094 a0010c0009t0001g0056 a0010c0009t0001g0225 |
3 | 350 | 0.0086 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978289 | TCCCAGGC others(38): Show |
T | intron_variant | MODIFIER | HG00673.hp1 HG02155.hp1 NA18967.hp1 others(1): Show |
a0001a0006a0011 | a0001c0002a0006c0007a0011c0019 | a0001c0002t0001a0001c0002t0002a0006c0007t0001others(1): Show | a0001c0002t0001g0152 a0001c0002t0002g0316 a0006c0007t0001g0208 others(1): Show |
4 | 350 | 0.0114 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978722 | GGGTAGGA others(38): Show |
G | intron_variant | MODIFIER | HG03239.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0043 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978761 | TCTCTGTG others(38): Show |
T | intron_variant | MODIFIER | HG01358.hp2 HG01516.hp2 HG01884.hp1 others(2): Show |
a0001a0003a0016others(1): Show | a0001c0002a0003c0003a0016c0065others(1): Show | a0001c0002t0001a0001c0002t0002a0003c0003t0001others(2): Show | a0001c0002t0001g0152 a0001c0002t0002g0276 a0003c0003t0001g0021 others(2): Show |
5 | 350 | 0.0143 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240978941 | TCTCTGGG others(38): Show |
T | intron_variant | MODIFIER | HG01358.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0276 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240979185 | AGGAGCCC others(38): Show |
A | intron_variant | MODIFIER | HG01167.hp2 | a0008 | a0008c0008 | a0008c0008t0002 | a0008c0008t0002g0251 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240979256 | TCTCTGGG others(38): Show |
T | intron_variant | MODIFIER | HG01358.hp2 HG01516.hp2 HG02155.hp1 others(8): Show |
a0001a0003a0006others(4): Show | a0001c0002a0003c0003a0006c0007others(5): Show | a0001c0002t0001a0001c0002t0002a0003c0003t0001others(6): Show | a0001c0002t0001g0131 a0001c0002t0001g0152 a0001c0002t0002g0276 others(8): Show |
11 | 350 | 0.0314 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240979525 | GGCTCTGG others(38): Show |
G | intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0181 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240979616 | GCTCTGGG others(38): Show |
G | intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0181 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240980155 | GTCTCTGG others(38): Show |
G | intron_variant | MODIFIER | HG01884.hp1 | a0030 | a0030c0031 | a0030c0031t0001 | a0030c0031t0001g0025 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | chr2 | TogoVar | |||||||
CROCC2_chr2_240901336_240998311 | 240980156 | TCTCTGGG others(38): Show |
T | intron_variant | MODIFIER | HG02109.hp2 | a0022 | a0022c0082 | a0022c0082t0001 | a0022c0082t0001g0111 | 1 | 350 | 0.0029 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240980185 | ACTCATCC others(38): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(12): Show |
a0001a0002a0003others(3): Show | a0001c0002a0001c0012a0002c0020others(4): Show | a0001c0002t0001a0001c0002t0002a0001c0012t0002others(5): Show | a0001c0002t0001g0181 a0001c0002t0002g0283 a0001c0002t0002g0318 others(12): Show |
15 | 350 | 0.0429 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240980265 | AGGAGCCC others(38): Show |
A | intron_variant | MODIFIER | HG02145.hp2 HG02723.hp1 HG02976.hp2 |
a0016a0017a0040 | a0016c0065a0017c0016a0040c0055 | a0016c0065t0001a0017c0016t0001a0040c0055t0001 | a0016c0065t0001g0161 a0017c0016t0001g0070 a0040c0055t0001g0169 |
3 | 350 | 0.0086 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CROCC2_chr2_240901336_240998311 | 240980336 | GCTCTGGG others(38): Show |
G | intron_variant | MODIFIER | HG03098.hp2 HG03139.hp1 |
a0012a0046 | a0012c0080a0046c0037 | a0012c0080t0001a0046c0037t0001 | a0012c0080t0001g0178 a0046c0037t0001g0231 |
2 | 350 | 0.0057 | -45 | c.440 others(64): Show |
CROCC2 | ENSG00000226321.6 | transcript | ENST00000690015.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |