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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
HBG1_chr11_5243269_5254857 | 5253698 | G | GCGCACAC others(4957): Show |
upstream_gene_variant | MODIFIER | NA18959.hp2 NA18978.hp2 NA19079.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 4 | 433 | 0.0092 | 4964 | c.-38 others(4975): Show |
HBG1 | ENSG00000213934.9 | transcript | ENST00000330597.5 | protein_coding | 3842 | chr11 | TogoVar | |||||||
HBG1_chr11_5243269_5254857 | 5253698 | G | GCGCACAC others(4957): Show |
upstream_gene_variant | MODIFIER | NA19063.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 433 | 0.0023 | 4964 | c.-38 others(4975): Show |
HBG1 | ENSG00000213934.9 | transcript | ENST00000330597.5 | protein_coding | 3842 | chr11 | TogoVar | |||||||
HBG2_chr11_5248188_5259781 | 5253698 | G | GCGCACAC others(4957): Show |
intron_variant | MODIFIER | NA18959.hp2 NA19079.hp2 NA19085.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 3 | 430 | 0.0070 | 4964 | c.316 others(4979): Show |
HBG2 | ENSG00000196565.15 | transcript | ENST00000336906.6 | protein_coding | 2/2 | chr11 | TogoVar | |||||||
HBG2_chr11_5248188_5259781 | 5253698 | G | GCGCACAC others(4957): Show |
intron_variant | MODIFIER | NA19063.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 | 1 | 430 | 0.0023 | 4964 | c.316 others(4979): Show |
HBG2 | ENSG00000196565.15 | transcript | ENST00000336906.6 | protein_coding | 2/2 | chr11 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1223139 | T | TCTCCCTG others(4957): Show |
intron_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0126 | 1 | 190 | 0.0053 | 4964 | c.719 others(4983): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SPAAR_chr9_35904490_35916686 | 35914283 | A | AGTGTGTG others(4958): Show |
downstream_gene_variant | MODIFIER | NA18977.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 420 | 0.0024 | 4965 | c.*35 others(4976): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2598 | chr9 | TogoVar | |||||||
SPAAR_chr9_35904490_35916686 | 35914283 | A | AGTGTGTG others(4958): Show |
downstream_gene_variant | MODIFIER | NA19005.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 420 | 0.0024 | 4965 | c.*35 others(4976): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2598 | chr9 | TogoVar | |||||||
SPAAR_chr9_35904490_35916686 | 35914283 | A | AGTGTGTG others(4958): Show |
downstream_gene_variant | MODIFIER | NA18953.hp1 NA18959.hp1 NA18963.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 6 | 420 | 0.0143 | 4965 | c.*35 others(4976): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2598 | chr9 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4959): Show |
intron_variant | MODIFIER | NA18943.hp2 NA18952.hp1 NA18970.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | 370 | 0.0081 | 4966 | c.891 others(4981): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4959): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 370 | 0.0027 | 4966 | c.891 others(4981): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4959): Show |
intron_variant | MODIFIER | HG01070.hp1 HG02015.hp1 HG02451.hp2 others(1): Show |
a0004a0005 | a0004c0005a0005c0008 | a0004c0005t0001a0005c0008t0001 | a0004c0005t0001g0080 a0004c0005t0001g0086 a0004c0005t0001g0087 others(1): Show |
4 | 336 | 0.0119 | 4966 | c.107 others(4983): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716489 | T | TGGGGGAG others(4960): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0049 | 1 | 170 | 0.0059 | 4967 | c.86- others(4980): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4960): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
a0004a0005a0006others(1): Show | a0004c0005a0005c0007a0005c0008others(3): Show | a0004c0005t0001a0005c0007t0002a0005c0008t0001others(3): Show | a0004c0005t0001g0079 a0004c0005t0001g0084 a0004c0005t0001g0088 others(24): Show |
27 | 336 | 0.0804 | 4967 | c.107 others(4984): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4960): Show |
intron_variant | MODIFIER | NA18951.hp2 | a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0108 | 1 | 336 | 0.0030 | 4967 | c.107 others(4984): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4960): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0007 | a0007c0012 | a0007c0012t0001 | a0007c0012t0001g0020 | 1 | 336 | 0.0030 | 4967 | c.107 others(4984): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4960): Show |
intron_variant | MODIFIER | HG03098.hp2 NA19240.hp2 |
a0002 | a0002c0024a0002c0025 | a0002c0024t0001a0002c0025t0001 | a0002c0024t0001g0081 a0002c0025t0001g0085 |
2 | 336 | 0.0060 | 4967 | c.107 others(4984): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4960): Show |
intron_variant | MODIFIER | HG02451.hp1 HG03486.hp2 |
a0007 | a0007c0012 | a0007c0012t0001 | a0007c0012t0001g0021 a0007c0012t0001g0022 |
2 | 336 | 0.0060 | 4967 | c.107 others(4984): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4961): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0218 | 1 | 344 | 0.0029 | 4968 | c.127 others(4985): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4961): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0122 | 1 | 370 | 0.0027 | 4968 | c.891 others(4983): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4961): Show |
intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 370 | 0.0027 | 4968 | c.891 others(4983): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4961): Show |
intron_variant | MODIFIER | NA18981.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 370 | 0.0027 | 4968 | c.891 others(4983): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4961): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0111 | 1 | 370 | 0.0027 | 4968 | c.891 others(4983): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
EHMT1_chr9_137614005_137841127 | 137716360 | T | TGTGGTGG others(4961): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0016 | a0001c0016t0001 | a0001c0016t0001g0029 | 1 | 170 | 0.0059 | 4968 | c.86- others(4981): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4961): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079 | 1 | 279 | 0.0036 | 4968 | c.215 others(4985): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31432069 | G | GGTGGACA others(4961): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0097 | 1 | 376 | 0.0027 | 4968 | c.101 others(4985): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31432146 | A | ATAGGGTG others(4961): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0008 | a0008c0022 | a0008c0022t0001 | a0008c0022t0001g0278 | 1 | 376 | 0.0027 | 4968 | c.101 others(4985): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | TogoVar | |||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4961): Show |
intron_variant | MODIFIER | NA18978.hp1 NA19003.hp1 |
a0005 | a0005c0007 | a0005c0007t0002 | a0005c0007t0002g0106 a0005c0007t0002g0107 |
2 | 336 | 0.0060 | 4968 | c.107 others(4985): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230338021 | G | GTTCTGTG others(4961): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0005 | a0005c0007 | a0005c0007t0002 | a0005c0007t0002g0109 | 1 | 336 | 0.0030 | 4968 | c.107 others(4985): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4963): Show |
intron_variant | MODIFIER | NA18953.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 344 | 0.0029 | 4970 | c.127 others(4987): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137716460 | T | TGGGGGAG others(4963): Show |
intron_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0032 | 1 | 170 | 0.0059 | 4970 | c.86- others(4983): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1222982 | T | TGCAGTGA others(4963): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0009 | a0009c0012 | a0009c0012t0001 | a0009c0012t0001g0166 | 1 | 190 | 0.0053 | 4970 | c.719 others(4989): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236714890 | T | TACCACTG others(4964): Show |
intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0043 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0198 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0222 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0201 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0186 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | NA18945.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0209 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | NA19003.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0202 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(1): Show | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0219 others(9): Show |
12 | 344 | 0.0349 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | NA18986.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0206 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ACTN2_chr1_236681499_236769631 | 236715026 | C | CCACTGAA others(4964): Show |
intron_variant | MODIFIER | HG01934.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0244 | 1 | 344 | 0.0029 | 4971 | c.127 others(4988): Show |
ACTN2 | ENSG00000077522.15 | transcript | ENST00000366578.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ADAP1_chr7_892900_959680 | 906503 | G | GGGAAAGG others(4965): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0011 | 1 | 14 | 0.0714 | 4972 | c.389 others(4989): Show |
ADAP1 | ENSG00000105963.15 | transcript | ENST00000265846.10 | protein_coding | 4/10 | chr7 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4965): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0038 | a0038c0045 | a0038c0045t0001 | a0038c0045t0001g0104 | 1 | 282 | 0.0036 | 4972 | c.299 others(4987): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4966): Show |
upstream_gene_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0153 | 1 | 251 | 0.0040 | 4973 | c.-45 others(4982): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
LRRC27_chr10_132327193_132386508 | 132364497 | C | ACTTACAT others(4968): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0005 | a0001c0005t0008 | a0001c0005t0008g0225 | 1 | 290 | 0.0035 | 4975 | c.129 others(4992): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | chr10 | TogoVar | |||||||
RTEL1_chr20_63653312_63701245 | 63693732 | T | TCCACCAC others(4968): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0016 | 1 | 60 | 0.0167 | 4975 | c.299 others(4992): Show |
RTEL1 | ENSG00000258366.12 | transcript | ENST00000360203.11 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
TNFRSF6B_chr20_63691652_63703684 | 63693732 | T | TCCACCAC others(4968): Show |
upstream_gene_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 33 | 0.0303 | 4975 | c.-30 others(4986): Show |
TNFRSF6B | ENSG00000243509.6 | transcript | ENST00000369996.3 | protein_coding | 2919 | chr20 | TogoVar | |||||||
ART1_chr11_3640128_3669416 | 3654590 | T | TTGTAAAT others(4969): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 1 | 394 | 0.0025 | 4976 | c.-52 others(4993): Show |
ART1 | ENSG00000129744.3 | transcript | ENST00000250693.2 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |