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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP30_chr1_161041946_161074891 | 161052792 | C | T | missense_variant | MODERATE | HG00735.hp1 | a0011 | a0011c0008 | a0011c0008t0001 | a0011c0008t0001g0258 | 1 | 390 | 0.0026 | 0 | c.670 others(3): Show |
p.Glu others(6): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 7/12 | 937/4342 | 670/3306 | 224/1101 | chr1 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119382312 | G | A | missense_variant | MODERATE | HG03471.hp1 HG03579.hp1 |
a0006a0007 | a0006c0011a0007c0012 | a0006c0011t0015a0007c0012t0001 | a0006c0011t0015g0013a0007c0012t0001g0050 | 2 | 310 | 0.0065 | 0 | c.452 others(3): Show |
p.Arg others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/12 | 974/9307 | 452/4335 | 151/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119402133 | C | A | missense_variant | MODERATE | NA18992.hp1 | a0015 | a0015c0013 | a0015c0013t0006 | a0015c0013t0006g0115 | 1 | 310 | 0.0032 | 0 | c.138 others(4): Show |
p.Pro others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 1903/9307 | 1381/4335 | 461/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119402349 | G | A | missense_variant | MODERATE | HG02486.hp2 | a0014 | a0014c0014 | a0014c0014t0058 | a0014c0014t0058g0003 | 1 | 310 | 0.0032 | 0 | c.159 others(4): Show |
p.Gly others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2119/9307 | 1597/4335 | 533/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119402370 | A | G | missense_variant | MODERATE | NA19043.hp1 | a0008 | a0008c0021 | a0008c0021t0001 | a0008c0021t0001g0068 | 1 | 310 | 0.0032 | 0 | c.161 others(4): Show |
p.Lys others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2140/9307 | 1618/4335 | 540/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119409550 | C | T | missense_variant | MODERATE | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
a0004a0006 | a0004c0007a0006c0011 | a0004c0007t0015a0004c0007t0044a0004c0007t0054others(1): Show | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | 310 | 0.0226 | 0 | c.170 others(4): Show |
p.Pro others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/12 | 2222/9307 | 1700/4335 | 567/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119409622 | A | G | missense_variant | MODERATE | NA21309.hp2 | a0013 | a0013c0020 | a0013c0020t0013 | a0013c0020t0013g0051 | 1 | 310 | 0.0032 | 0 | c.177 others(4): Show |
p.Glu others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/12 | 2294/9307 | 1772/4335 | 591/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119414273 | C | A | missense_variant | MODERATE | HG02723.hp1 | a0012 | a0012c0015 | a0012c0015t0035 | a0012c0015t0035g0237 | 1 | 310 | 0.0032 | 0 | c.234 others(4): Show |
p.Pro others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2866/9307 | 2344/4335 | 782/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119414288 | C | T | missense_variant | MODERATE | NA19005.hp1 | a0011 | a0011c0019 | a0011c0019t0005 | a0011c0019t0005g0155 | 1 | 310 | 0.0032 | 0 | c.235 others(4): Show |
p.Pro others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2881/9307 | 2359/4335 | 787/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119414336 | G | A | missense_variant | MODERATE | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
a0001a0003a0004others(9): Show | a0001c0001a0001c0002a0001c0004others(14): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(70): Show | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(255): Show | 260 | 310 | 0.8387 | 0 | c.240 others(4): Show |
p.Gly others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2929/9307 | 2407/4335 | 803/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119414441 | G | C | missense_variant | MODERATE | HG03654.hp2 | a0009 | a0009c0017 | a0009c0017t0019 | a0009c0017t0019g0185 | 1 | 310 | 0.0032 | 0 | c.251 others(4): Show |
p.Glu others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3034/9307 | 2512/4335 | 838/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119415185 | G | A | missense_variant | MODERATE | HG01099.hp1 HG01106.hp2 HG01884.hp2 others(9): Show |
a0003a0013 | a0003c0006a0003c0009a0013c0020 | a0003c0006t0001a0003c0006t0013a0003c0006t0022others(4): Show | a0003c0006t0001g0159a0003c0006t0001g0161a0003c0006t0013g0006others(9): Show | 12 | 310 | 0.0387 | 0 | c.325 others(4): Show |
p.Ala others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3778/9307 | 3256/4335 | 1086/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119415387 | A | G | missense_variant | MODERATE | HG00735.hp2 | a0010 | a0010c0016 | a0010c0016t0004 | a0010c0016t0004g0166 | 1 | 310 | 0.0032 | 0 | c.345 others(4): Show |
p.Asp others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3980/9307 | 3458/4335 | 1153/1444 | chr3 | TogoVar | ||
ARHGAP31_chr3_119289383_119425714 | 119416025 | G | A | missense_variant | MODERATE | HG02155.hp2 NA18945.hp2 NA19064.hp2 others(2): Show |
a0005 | a0005c0008 | a0005c0008t0002 | a0005c0008t0002g0106a0005c0008t0002g0107a0005c0008t0002g0114others(2): Show | 5 | 310 | 0.0161 | 0 | c.409 others(4): Show |
p.Val others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4618/9307 | 4096/4335 | 1366/1444 | chr3 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128969478 | G | A | missense_variant | MODERATE | HG02559.hp2 | a0011 | a0011c0021 | a0011c0021t0006 | a0011c0021t0006g0227 | 1 | 398 | 0.0025 | 0 | c.573 others(4): Show |
p.Pro others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 5862/10280 | 5735/6306 | 1912/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128969631 | C | G | missense_variant | MODERATE | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
a0002a0011 | a0002c0004a0002c0007a0002c0008others(2): Show | a0002c0004t0001a0002c0004t0005a0002c0004t0010others(9): Show | a0002c0004t0001g0204a0002c0004t0001g0205a0002c0004t0001g0206others(30): Show | 33 | 398 | 0.0829 | 0 | c.558 others(4): Show |
p.Ser others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 5709/10280 | 5582/6306 | 1861/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128970037 | G | A | missense_variant | MODERATE | HG02257.hp2 | a0012 | a0012c0023 | a0012c0023t0005 | a0012c0023t0005g0239 | 1 | 398 | 0.0025 | 0 | c.517 others(4): Show |
p.Arg others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 5303/10280 | 5176/6306 | 1726/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128970084 | A | G | missense_variant | MODERATE | NA18963.hp1 | a0013 | a0013c0031 | a0013c0031t0004 | a0013c0031t0004g0155 | 1 | 398 | 0.0025 | 0 | c.512 others(4): Show |
p.Leu others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 5256/10280 | 5129/6306 | 1710/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128970581 | C | G | missense_variant | MODERATE | HG02559.hp2 | a0011 | a0011c0021 | a0011c0021t0006 | a0011c0021t0006g0227 | 1 | 398 | 0.0025 | 0 | c.463 others(4): Show |
p.Met others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 4759/10280 | 4632/6306 | 1544/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128970733 | C | T | missense_variant | MODERATE | HG03471.hp1 | a0014 | a0014c0036 | a0014c0036t0020 | a0014c0036t0020g0193 | 1 | 398 | 0.0025 | 0 | c.448 others(4): Show |
p.Asp others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 4607/10280 | 4480/6306 | 1494/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128970983 | G | C | missense_variant | MODERATE | HG03471.hp1 | a0014 | a0014c0036 | a0014c0036t0020 | a0014c0036t0020g0193 | 1 | 398 | 0.0025 | 0 | c.423 others(4): Show |
p.His others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 23/23 | 4357/10280 | 4230/6306 | 1410/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128972458 | G | A | missense_variant | MODERATE | HG01943.hp2 | a0015 | a0015c0025 | a0015c0025t0005 | a0015c0025t0005g0229 | 1 | 398 | 0.0025 | 0 | c.404 others(4): Show |
p.His others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 22/23 | 4175/10280 | 4048/6306 | 1350/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128972596 | C | G | missense_variant | MODERATE | HG01168.hp2 | a0016 | a0016c0030 | a0016c0030t0001 | a0016c0030t0001g0049 | 1 | 398 | 0.0025 | 0 | c.391 others(4): Show |
p.Asp others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 22/23 | 4037/10280 | 3910/6306 | 1304/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128972712 | G | A | missense_variant | MODERATE | HG01891.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
a0003 | a0003c0006a0003c0035 | a0003c0006t0002a0003c0006t0004a0003c0035t0004 | a0003c0006t0002g0091a0003c0006t0002g0092a0003c0006t0002g0093others(2): Show | 5 | 398 | 0.0126 | 0 | c.379 others(4): Show |
p.Ser others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 22/23 | 3921/10280 | 3794/6306 | 1265/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128972821 | A | G | missense_variant | MODERATE | HG02451.hp2 HG02922.hp2 HG03516.hp2 |
a0004 | a0004c0009 | a0004c0009t0001 | a0004c0009t0001g0070a0004c0009t0001g0237a0004c0009t0001g0238 | 3 | 398 | 0.0075 | 0 | c.368 others(4): Show |
p.Ser others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 22/23 | 3812/10280 | 3685/6306 | 1229/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128973045 | T | C | missense_variant | MODERATE | HG02809.hp2 HG03209.hp1 HG03540.hp1 |
a0005 | a0005c0011 | a0005c0011t0008a0005c0011t0021 | a0005c0011t0008g0072a0005c0011t0008g0073a0005c0011t0021g0071 | 3 | 398 | 0.0075 | 0 | c.346 others(4): Show |
p.Glu others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 22/23 | 3588/10280 | 3461/6306 | 1154/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128974198 | T | A | missense_variant | MODERATE | NA19005.hp2 | a0017 | a0017c0026 | a0017c0026t0001 | a0017c0026t0001g0286 | 1 | 398 | 0.0025 | 0 | c.299 others(4): Show |
p.Glu others(7): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 21/23 | 3126/10280 | 2999/6306 | 1000/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128974493 | C | T | missense_variant | MODERATE | HG01884.hp1 | a0010 | a0010c0018 | a0010c0018t0037 | a0010c0018t0037g0369 | 1 | 398 | 0.0025 | 0 | c.270 others(4): Show |
p.Val others(6): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 21/23 | 2831/10280 | 2704/6306 | 902/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128974684 | T | C | missense_variant | MODERATE | HG01952.hp1 | a0009 | a0009c0027 | a0009c0027t0001 | a0009c0027t0001g0234 | 1 | 398 | 0.0025 | 0 | c.251 others(4): Show |
p.Tyr others(6): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 21/23 | 2640/10280 | 2513/6306 | 838/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128974733 | C | T | missense_variant | MODERATE | HG03654.hp1 | a0018 | a0018c0017 | a0018c0017t0001 | a0018c0017t0001g0279 | 1 | 398 | 0.0025 | 0 | c.246 others(4): Show |
p.Glu others(6): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 21/23 | 2591/10280 | 2464/6306 | 822/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128974909 | T | C | missense_variant | MODERATE | NA18940.hp1 | a0019 | a0019c0028 | a0019c0028t0001 | a0019c0028t0001g0306 | 1 | 398 | 0.0025 | 0 | c.228 others(4): Show |
p.Asn others(6): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 21/23 | 2415/10280 | 2288/6306 | 763/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128974916 | G | A | missense_variant | MODERATE | HG04204.hp2 | a0008 | a0008c0029 | a0008c0029t0023 | a0008c0029t0023g0359 | 1 | 398 | 0.0025 | 0 | c.228 others(4): Show |
p.Arg others(6): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 21/23 | 2408/10280 | 2281/6306 | 761/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 128980596 | G | A | missense_variant | MODERATE | HG01993.hp2 | a0007 | a0007c0037 | a0007c0037t0004 | a0007c0037t0004g0161 | 1 | 398 | 0.0025 | 0 | c.193 others(4): Show |
p.Leu others(6): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 18/23 | 2060/10280 | 1933/6306 | 645/2101 | chr11 | TogoVar | ||
ARHGAP32_chr11_128960060_129197325 | 129164324 | C | T | missense_variant | MODERATE | HG02698.hp2 HG04204.hp1 |
a0006 | a0006c0012 | a0006c0012t0003 | a0006c0012t0003g0326a0006c0012t0003g0342 | 2 | 398 | 0.0050 | 0 | c.220 others(3): Show |
p.Ala others(5): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/23 | 347/10280 | 220/6306 | 74/2101 | chr11 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35780977 | G | A | missense_variant | MODERATE | NA19089.hp2 | a0007 | a0007c0019 | a0007c0019t0001 | a0007c0019t0001g0004 | 1 | 420 | 0.0024 | 0 | c.887 others(3): Show |
p.Arg others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 11/21 | 982/4352 | 887/3864 | 296/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35782380 | T | A | missense_variant | MODERATE | NA18951.hp1 | a0019 | a0019c0020 | a0019c0020t0001 | a0019c0020t0001g0075 | 1 | 420 | 0.0024 | 0 | c.109 others(4): Show |
p.Phe others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 13/21 | 1188/4352 | 1093/3864 | 365/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35782830 | C | A | missense_variant | MODERATE | HG04228.hp1 | a0018 | a0018c0032 | a0018c0032t0001 | a0018c0032t0001g0003 | 1 | 420 | 0.0024 | 0 | c.138 others(4): Show |
p.Ala others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 15/21 | 1477/4352 | 1382/3864 | 461/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35784176 | A | G | missense_variant | MODERATE | HG00597.hp2 | a0017 | a0017c0039 | a0017c0039t0001 | a0017c0039t0001g0008 | 1 | 420 | 0.0024 | 0 | c.142 others(4): Show |
p.Met others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 16/21 | 1521/4352 | 1426/3864 | 476/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35784970 | A | G | missense_variant | MODERATE | NA18951.hp1 | a0019 | a0019c0020 | a0019c0020t0001 | a0019c0020t0001g0075 | 1 | 420 | 0.0024 | 0 | c.158 others(4): Show |
p.Arg others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 17/21 | 1680/4352 | 1585/3864 | 529/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35785271 | A | T | missense_variant | MODERATE | HG00673.hp2 | a0008 | a0008c0030 | a0008c0030t0001 | a0008c0030t0001g0020 | 1 | 420 | 0.0024 | 0 | c.180 others(4): Show |
p.Ser others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 18/21 | 1899/4352 | 1804/3864 | 602/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35786677 | G | C | missense_variant | MODERATE | HG02723.hp1 | a0009 | a0009c0024 | a0009c0024t0001 | a0009c0024t0001g0049 | 1 | 420 | 0.0024 | 0 | c.220 others(4): Show |
p.Arg others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2302/4352 | 2207/3864 | 736/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35786907 | G | A | missense_variant | MODERATE | NA18906.hp1 NA20300.hp2 |
a0006 | a0006c0016 | a0006c0016t0001 | a0006c0016t0001g0029 | 2 | 420 | 0.0048 | 0 | c.243 others(4): Show |
p.Ala others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2532/4352 | 2437/3864 | 813/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35786953 | C | G | missense_variant | MODERATE | NA18947.hp1 | a0015 | a0015c0029 | a0015c0029t0001 | a0015c0029t0001g0031 | 1 | 420 | 0.0024 | 0 | c.248 others(4): Show |
p.Pro others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2578/4352 | 2483/3864 | 828/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35786955 | G | A | missense_variant | MODERATE | HG01261.hp2 | a0014 | a0014c0034 | a0014c0034t0001 | a0014c0034t0001g0003 | 1 | 420 | 0.0024 | 0 | c.248 others(4): Show |
p.Gly others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2580/4352 | 2485/3864 | 829/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35787042 | A | G | missense_variant | MODERATE | NA19089.hp2 | a0007 | a0007c0019 | a0007c0019t0001 | a0007c0019t0001g0004 | 1 | 420 | 0.0024 | 0 | c.257 others(4): Show |
p.Ser others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 20/21 | 2667/4352 | 2572/3864 | 858/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35787209 | C | A | missense_variant | MODERATE | HG02523.hp1 NA18955.hp2 NA18995.hp1 others(2): Show |
a0003 | a0003c0009 | a0003c0009t0001 | a0003c0009t0001g0023a0003c0009t0001g0082a0003c0009t0001g0083 | 5 | 420 | 0.0119 | 0 | c.264 others(4): Show |
p.Leu others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2739/4352 | 2644/3864 | 882/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35787362 | C | T | missense_variant | MODERATE | HG04115.hp1 | a0010 | a0010c0028 | a0010c0028t0001 | a0010c0028t0001g0004 | 1 | 420 | 0.0024 | 0 | c.279 others(4): Show |
p.Arg others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2892/4352 | 2797/3864 | 933/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35787383 | G | C | missense_variant | MODERATE | HG01943.hp1 | a0013 | a0013c0026 | a0013c0026t0001 | a0013c0026t0001g0002 | 1 | 420 | 0.0024 | 0 | c.281 others(4): Show |
p.Gly others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2913/4352 | 2818/3864 | 940/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35787444 | G | C | missense_variant | MODERATE | HG00544.hp2 HG00558.hp1 NA18981.hp2 others(2): Show |
a0004 | a0004c0008 | a0004c0008t0001 | a0004c0008t0001g0004 | 5 | 420 | 0.0119 | 0 | c.287 others(4): Show |
p.Gly others(6): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 2974/4352 | 2879/3864 | 960/1287 | chr19 | TogoVar | ||
ARHGAP33_chr19_35770564_35793822 | 35787567 | C | T | missense_variant | MODERATE | HG02630.hp1 NA20129.hp1 |
a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0025a0005c0015t0001g0040 | 2 | 420 | 0.0048 | 0 | c.300 others(4): Show |
p.Ala others(7): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 21/21 | 3097/4352 | 3002/3864 | 1001/1287 | chr19 | TogoVar |