regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(27): Show |
A | intron_variant | MODIFIER | HG02257.hp2 HG03098.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0030a0001c0002t0053 | a0001c0001t0030g0277a0001c0002t0053g0127 | 2 | 298 | 0.0067 | -34 | c.-18 others(55): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144619608 | ATGTCCGT others(27): Show |
A | intron_variant | MODIFIER | HG02258.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | 246 | 0.0081 | -34 | c.-81 others(53): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38655088 | CAGAACCG others(27): Show |
C | downstream_gene_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156 | 1 | 350 | 0.0029 | -34 | c.*52 others(45): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 4436 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728238 | GCAGTTGG others(27): Show |
G | intron_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0213 | 1 | 286 | 0.0035 | -34 | c.154 others(53): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875103 | CTCTCTGT others(27): Show |
C | intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0002 | a0002c0002t0035 | a0002c0002t0035g0039 | 1 | 286 | 0.0035 | -34 | c.384 others(53): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(27): Show |
A | intron_variant | MODIFIER | HG03688.hp1 | a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0125 | 1 | 286 | 0.0035 | -34 | c.385 others(51): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12963563 | TCAATGCT others(27): Show |
T | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(32): Show |
a0001a0004 | a0001c0001a0001c0004a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0016a0001c0001t0001g0117a0001c0001t0001g0136others(32): Show | 35 | 230 | 0.1522 | -34 | c.152 others(53): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1087530 | TGGGAACC others(27): Show |
T | downstream_gene_variant | MODIFIER | HG02615.hp1 HG02717.hp2 |
a0012 | a0012c0027 | a0012c0027t0009 | a0012c0027t0009g0034 | 2 | 418 | 0.0048 | -34 | c.*15 others(45): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 903 | chr19 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | TTATATAT others(27): Show |
T | intron_variant | MODIFIER | NA19005.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 144 | 0.0069 | -34 | c.588 others(55): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590835 | AGAAAAGA others(27): Show |
A | intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0144 | 1 | 144 | 0.0069 | -34 | c.588 others(53): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | CGTGTGTG others(27): Show |
C | intron_variant | MODIFIER | HG03098.hp2 | a0002 | a0002c0008 | a0002c0008t0018 | a0002c0008t0018g0007 | 1 | 228 | 0.0044 | -34 | c.319 others(55): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154136245 | CTAAAGTA others(27): Show |
C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
a0002a0006a0007others(2): Show | a0002c0002a0002c0003a0002c0007others(6): Show | a0002c0002t0003a0002c0002t0005a0002c0002t0006others(30): Show | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(106): Show | 110 | 283 | 0.3887 | -34 | c.126 others(53): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671710 | ATATATAT others(27): Show |
A | intron_variant | MODIFIER | HG02074.hp2 HG02615.hp2 HG03831.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0021a0002c0002others(1): Show | a0001c0001t0001a0001c0021t0007a0002c0002t0001others(2): Show | a0001c0001t0001g0036a0001c0021t0007g0178a0002c0002t0001g0003others(2): Show | 5 | 188 | 0.0266 | -34 | c.-11 others(53): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671712 | ATATATAT others(27): Show |
A | intron_variant | MODIFIER | HG02572.hp2 HG03492.hp2 |
a0002a0007 | a0002c0032a0007c0009 | a0002c0032t0002a0007c0009t0002 | a0002c0032t0002g0065a0007c0009t0002g0047 | 2 | 188 | 0.0106 | -34 | c.-11 others(53): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671714 | ATATATAT others(27): Show |
A | intron_variant | MODIFIER | HG03225.hp1 NA21309.hp2 |
a0003a0004 | a0003c0007a0004c0050 | a0003c0007t0001a0004c0050t0005 | a0003c0007t0001g0045a0004c0050t0005g0046 | 2 | 188 | 0.0106 | -34 | c.-11 others(53): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741375 | GTGTGTGT others(27): Show |
G | intron_variant | MODIFIER | HG02723.hp2 | a0035 | a0035c0076 | a0035c0076t0001 | a0035c0076t0001g0125 | 1 | 188 | 0.0053 | -34 | c.34- others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741383 | GTGTATAT others(27): Show |
G | intron_variant | MODIFIER | NA19091.hp1 NA19091.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0002 | a0001c0001t0001g0023a0002c0003t0002g0055 | 2 | 188 | 0.0106 | -34 | c.34- others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF2_chr1_155941854_155983547 | 155964157 | AAAAAAAA others(27): Show |
A | intron_variant | MODIFIER | NA18993.hp2 NA19054.hp2 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0006g0106 | 3 | 284 | 0.0106 | -34 | c.724 others(49): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149608262 | CTGACATA others(27): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
a0001a0002a0003others(19): Show | a0001c0002a0001c0005a0001c0030others(32): Show | a0001c0002t0004a0001c0002t0005a0001c0002t0006others(69): Show | a0001c0002t0004g0352a0001c0002t0005g0367a0001c0002t0005g0368others(365): Show | 382 | 394 | 0.9695 | -34 | c.311 others(51): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130833383 | GAAAGAAA others(27): Show |
G | upstream_gene_variant | MODIFIER | NA18948.hp2 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0128 | 1 | 144 | 0.0069 | -34 | c.-35 others(45): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3530 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130833402 | AAAAGAAA others(27): Show |
A | upstream_gene_variant | MODIFIER | HG02895.hp1 | a0007 | a0007c0017 | a0007c0017t0001 | a0007c0017t0001g0108 | 1 | 144 | 0.0069 | -34 | c.-35 others(45): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3511 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130833407 | AAAAGAAA others(27): Show |
A | upstream_gene_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0087 | 1 | 144 | 0.0069 | -34 | c.-35 others(45): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3506 | chr2 | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136686589 | TGTGTGTA others(27): Show |
T | intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0116 | 1 | 247 | 0.0041 | -34 | c.124 others(51): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111196742 | TAAGCTGA others(27): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(84): Show | 87 | 274 | 0.3175 | -34 | c.253 others(51): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111221412 | GATGTCTA others(27): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | 274 | 0.0292 | -34 | c.670 others(51): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156813063 | TATATATA others(27): Show |
T | intron_variant | MODIFIER | HG03579.hp2 | a0029 | a0029c0013 | a0029c0013t0009 | a0029c0013t0009g0044 | 1 | 150 | 0.0067 | -34 | c.179 others(55): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156934912 | TTATATAT others(27): Show |
T | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0121 | 1 | 150 | 0.0067 | -34 | c.213 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157154490 | TACAGGGT others(27): Show |
T | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0017a0002c0003others(1): Show | a0001c0001t0001a0001c0017t0020a0002c0003t0002others(1): Show | a0001c0001t0001g0065a0001c0001t0001g0120a0001c0001t0001g0145others(3): Show | 6 | 150 | 0.0400 | -34 | c.308 others(53): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 8/19 | chr6 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235173757 | AAAAAAAA others(27): Show |
A | intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0099 | 1 | 272 | 0.0037 | -34 | c.366 others(52): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 22/23 | chr1 | TogoVar | ||||||
ARL14EPL_chr5_116027472_116064489 | 116053024 | TTAATTTC others(27): Show |
T | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0079 | 1 | 462 | 0.0022 | -34 | c.97- others(47): Show |
ARL14EPL | ENSG00000268223.7 | transcript | ENST00000686077.1 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARL2BP_chr16_57240259_57258635 | 57257541 | GGCGTCCA others(27): Show |
G | downstream_gene_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 372 | 0.0027 | -34 | c.*52 others(45): Show |
ARL2BP | ENSG00000102931.8 | transcript | ENST00000219204.8 | protein_coding | 3907 | chr16 | TogoVar | ||||||
ARL6IP4_chr12_122975681_122987909 | 122981407 | ATGTGAGG others(27): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02615.hp2 HG02965.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0005a0002c0002t0001g0017 | 5 | 356 | 0.0140 | -34 | c.160 others(49): Show |
ARL6IP4 | ENSG00000182196.14 | transcript | ENST00000315580.10 | protein_coding | 2/5 | chr12 | TogoVar | ||||||
ARL8B_chr3_5117292_5185911 | 5118268 | GTATATAT others(27): Show |
G | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(236): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(233): Show | 239 | 304 | 0.7862 | -34 | c.-41 others(45): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 4023 | chr3 | TogoVar | ||||||
ARL8B_chr3_5117292_5185911 | 5174665 | AATATATG others(27): Show |
A | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(140): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(8): Show | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(135): Show | 143 | 304 | 0.4704 | -34 | c.511 others(49): Show |
ARL8B | ENSG00000134108.14 | transcript | ENST00000256496.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138222467 | TAGGAAGT others(27): Show |
T | intron_variant | MODIFIER | NA18963.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0220 | 1 | 246 | 0.0041 | -34 | c.194 others(49): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARMC8_chr3_138182301_138303373 | 138229150 | ATATATAT others(27): Show |
A | intron_variant | MODIFIER | HG02615.hp1 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0042a0001c0001t0009g0048 | 2 | 246 | 0.0081 | -34 | c.528 others(49): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARSH_chrX_3001546_3039111 | 3012552 | AAAAAAAA others(27): Show |
A | intron_variant | MODIFIER | HG03927.hp2 | a0006 | a0006c0018 | a0006c0018t0008 | a0006c0018t0008g0023 | 1 | 248 | 0.0040 | -34 | c.215 others(49): Show |
ARSH | ENSG00000205667.3 | transcript | ENST00000381130.3 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARSJ_chr4_113895284_113984647 | 113924032 | TATAAATA others(27): Show |
T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0006 | 2 | 350 | 0.0057 | -34 | c.399 others(53): Show |
ARSJ | ENSG00000180801.14 | transcript | ENST00000315366.8 | protein_coding | 1/1 | chr4 | TogoVar | ||||||
ARSJ_chr4_113895284_113984647 | 113924056 | AATATATA others(27): Show |
A | intron_variant | MODIFIER | HG02109.hp2 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0018 | a0001c0001t0002g0135a0001c0001t0018g0048 | 2 | 350 | 0.0057 | -34 | c.399 others(53): Show |
ARSJ | ENSG00000180801.14 | transcript | ENST00000315366.8 | protein_coding | 1/1 | chr4 | TogoVar | ||||||
AS3MT_chr10_102864470_102906899 | 102885495 | ATTTTTTT others(27): Show |
A | intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0289 | 1 | 362 | 0.0028 | -34 | c.886 others(51): Show |
AS3MT | ENSG00000214435.9 | transcript | ENST00000369880.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ASB15_chr7_123596821_123644481 | 123620524 | ATATATAT others(27): Show |
A | intron_variant | MODIFIER | HG02886.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0007a0001c0002t0001g0119a0001c0002t0001g0120 | 4 | 380 | 0.0105 | -34 | c.451 others(51): Show |
ASB15 | ENSG00000146809.14 | transcript | ENST00000451215.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ASB15_chr7_123596821_123644481 | 123620526 | ATATATAT others(27): Show |
A | intron_variant | MODIFIER | HG02622.hp2 HG02818.hp2 HG03041.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0122 | 3 | 380 | 0.0079 | -34 | c.451 others(51): Show |
ASB15 | ENSG00000146809.14 | transcript | ENST00000451215.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ASB1_chr2_238421927_238457250 | 238450995 | CCGCTCCA others(27): Show |
C | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(17): Show | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 159 | 416 | 0.3822 | -34 | c.*45 others(45): Show |
ASB1 | ENSG00000065802.12 | transcript | ENST00000264607.9 | protein_coding | 5/5 | 4553 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||
ASB5_chr4_176208673_176274222 | 176219541 | TATGTATG others(27): Show |
T | intron_variant | MODIFIER | NA18961.hp2 NA19090.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0227a0001c0001t0001g0346 | 2 | 410 | 0.0049 | -34 | c.670 others(51): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | TogoVar | ||||||
ASCC1_chr10_72091032_72221276 | 72198065 | GGGAGGGG others(27): Show |
G | intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0021 | 1 | 216 | 0.0046 | -34 | c.311 others(51): Show |
ASCC1 | ENSG00000138303.19 | transcript | ENST00000672957.1 | protein_coding | 4/9 | chr10 | TogoVar | ||||||
ASCC1_chr10_72091032_72221276 | 72198071 | GGGAACGA others(27): Show |
G | intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145 | 1 | 216 | 0.0046 | -34 | c.311 others(51): Show |
ASCC1 | ENSG00000138303.19 | transcript | ENST00000672957.1 | protein_coding | 4/9 | chr10 | TogoVar | ||||||
ASCC1_chr10_72091032_72221276 | 72218163 | AAAATATA others(27): Show |
A | upstream_gene_variant | MODIFIER | HG02976.hp1 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0087 | 2 | 216 | 0.0093 | -34 | c.-20 others(45): Show |
ASCC1 | ENSG00000138303.19 | transcript | ENST00000672957.1 | protein_coding | 1888 | chr10 | TogoVar | ||||||
ASDURF_chr2_189656459_189671401 | 189665596 | GTGTATAT others(27): Show |
G | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 340 | 0.0029 | -34 | c.220 others(49): Show |
ASDURF | ENSG00000286053.2 | transcript | ENST00000607829.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ASGR1_chr17_7168431_7184370 | 7168751 | GCCAACAT others(27): Show |
G | downstream_gene_variant | MODIFIER | NA18994.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0008 | 1 | 442 | 0.0023 | -34 | c.*48 others(45): Show |
ASGR1 | ENSG00000141505.12 | transcript | ENST00000269299.8 | protein_coding | 4679 | chr17 | TogoVar | ||||||
ASMT_chrX_1610059_1648081 | 1610502 | ACTCCAGC others(27): Show |
A | upstream_gene_variant | MODIFIER | HG02615.hp1 HG02818.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0134a0001c0001t0003g0090 | 2 | 223 | 0.0090 | -34 | c.-46 others(45): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 4556 | chrX | TogoVar |