Item | Value |
---|---|
geneid | 3617 |
ensemblid | ENSG00000112706.12 |
hgncid | 6055 |
symbol | IMPG1 |
name | interphotoreceptor matrix proteoglycan 1 |
refseq_nuc | NM_001563.4 |
refseq_prot | NP_001554.2 |
ensembl_nuc | ENST00000369950.8 |
ensembl_prot | ENSP00000358966.3 |
mane_status | MANE Select |
chr | chr6 |
start | 75921114 |
end | 76072662 |
strand | - |
ver | v1.2 |
region | chr6:75921114-76072662 |
region5000 | chr6:75916114-76077662 |
regionname0 | IMPG1_chr6_75921114_76072662 |
regionname5000 | IMPG1_chr6_75916114_76077662 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 797 | 89 | 31 | 8 | 45 | 0 | 5 | 31 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0002 | 1/0 | 797 | 57 | 23 | 9 | 14 | 3 | 7 | 11 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0003 | 0/0 | 797 | 37 | 7 | 12 | 14 | 1 | 3 | 12 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0004 | 0/0 | 797 | 19 | 0 | 0 | 19 | 0 | 0 | 13 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0005 | 0/1 | 797 | 14 | 0 | 8 | 1 | 2 | 2 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0006 | 0/0 | 797 | 14 | 0 | 3 | 8 | 1 | 2 | 6 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0007 | 0/0 | 797 | 13 | 6 | 6 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0008 | 0/0 | 797 | 11 | 0 | 4 | 7 | 0 | 0 | 6 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0009 | 0/0 | 797 | 10 | 3 | 0 | 7 | 0 | 0 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0010 | 0/0 | 797 | 8 | 0 | 3 | 4 | 1 | 0 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0011 | 0/0 | 797 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0012 | 0/0 | 797 | 5 | 1 | 3 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0013 | 0/0 | 797 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0014 | 0/0 | 797 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0015 | 0/0 | 797 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0016 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0017 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0018 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0019 | 0/0 | 797 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0020 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0021 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0022 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0023 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0024 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
a0025 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | MYLET others(792): Show |
chr6 | 75916114 | 76077662 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2391 | 84 | 26 | 8 | 45 | 0 | 5 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0001c0016 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0001c0018 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0001c0026 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0002c0002 | 1/0 | 2391 | 57 | 23 | 9 | 14 | 3 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0003c0003 | 0/0 | 2391 | 35 | 5 | 12 | 14 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0003c0015 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0004c0004 | 0/0 | 2391 | 19 | 0 | 0 | 19 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0005c0006 | 0/1 | 2391 | 14 | 0 | 8 | 1 | 2 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0006c0005 | 0/0 | 2391 | 14 | 0 | 3 | 8 | 1 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0007c0007 | 0/0 | 2391 | 13 | 6 | 6 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0008c0008 | 0/0 | 2391 | 11 | 0 | 4 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0009c0009 | 0/0 | 2391 | 10 | 3 | 0 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0010c0010 | 0/0 | 2391 | 8 | 0 | 3 | 4 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0011c0011 | 0/0 | 2391 | 6 | 0 | 2 | 0 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0012c0012 | 0/0 | 2391 | 5 | 1 | 3 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0013c0013 | 0/0 | 2391 | 4 | 0 | 0 | 4 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0014c0014 | 0/0 | 2391 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0015c0017 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0016c0025 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0017c0028 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0018c0029 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0019c0019 | 0/0 | 2391 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0020c0024 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0021c0023 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0022c0021 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0023c0020 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0024c0022 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 | ||
a0025c0027 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | ATGTA others(2386): Show |
chr6 | 75916114 | 76077662 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3543 | 71 | 16 | 7 | 44 | 0 | 4 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0001c0001t0005 | 0/0 | 3547 | 10 | 9 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3542): Show |
chr6 | 75916114 | 76077662 |
a0001c0001t0009 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0001c0001t0010 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0001c0001t0012 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0001c0016t0005 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3542): Show |
chr6 | 75916114 | 76077662 |
a0001c0018t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0001c0026t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0002c0002t0001 | 1/0 | 3543 | 53 | 19 | 9 | 14 | 3 | 7 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0002c0002t0005 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3542): Show |
chr6 | 75916114 | 76077662 |
a0002c0002t0007 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0002c0002t0013 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0003c0003t0001 | 0/0 | 3543 | 29 | 3 | 11 | 13 | 1 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0003c0003t0002 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3534): Show |
chr6 | 75916114 | 76077662 |
a0003c0003t0006 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0003c0003t0008 | 0/0 | 3543 | 2 | 0 | 0 | 0 | 0 | 2 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0003c0003t0014 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0003c0015t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0004c0004t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0004c0004t0002 | 0/0 | 3539 | 18 | 0 | 0 | 18 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3534): Show |
chr6 | 75916114 | 76077662 |
a0005c0006t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0005c0006t0003 | 0/1 | 3543 | 13 | 0 | 8 | 1 | 2 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0006c0005t0001 | 0/0 | 3543 | 6 | 0 | 1 | 3 | 1 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0006c0005t0002 | 0/0 | 3539 | 5 | 0 | 0 | 5 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3534): Show |
chr6 | 75916114 | 76077662 |
a0006c0005t0006 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0006c0005t0008 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0006c0005t0011 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0007c0007t0004 | 0/0 | 3543 | 13 | 6 | 6 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0008c0008t0001 | 0/0 | 3543 | 11 | 0 | 4 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0009c0009t0001 | 0/0 | 3543 | 9 | 2 | 0 | 7 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0009c0009t0007 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0010c0010t0001 | 0/0 | 3543 | 8 | 0 | 3 | 4 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0011c0011t0003 | 0/0 | 3543 | 6 | 0 | 2 | 0 | 1 | 3 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0012c0012t0004 | 0/0 | 3543 | 5 | 1 | 3 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0013c0013t0001 | 0/0 | 3543 | 4 | 0 | 0 | 4 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0014c0014t0001 | 0/0 | 3543 | 3 | 0 | 0 | 3 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0015c0017t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0016c0025t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0017c0028t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0018c0029t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0019c0019t0003 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0020c0024t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0021c0023t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0022c0021t0002 | 0/0 | 3539 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3534): Show |
chr6 | 75916114 | 76077662 |
a0023c0020t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0024c0022t0001 | 0/0 | 3543 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
a0025c0027t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | AGACA others(3538): Show |
chr6 | 75916114 | 76077662 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0016t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0016t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0018t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0018t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0001c0026t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0250 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0002c0002t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0008g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0008g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0003t0014g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0015t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0003c0015t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0004c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0005c0006t0003g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0008g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0006c0005t0011g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0007c0007t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0008c0008t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0009c0009t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0010c0010t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0011c0011t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0011c0011t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0011c0011t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0011c0011t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0011c0011t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0011c0011t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0012c0012t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0012c0012t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0012c0012t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0012c0012t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0012c0012t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0013c0013t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0013c0013t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0013c0013t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0013c0013t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0014c0014t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0014c0014t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0014c0014t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0015c0017t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0015c0017t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0016c0025t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0017c0028t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0018c0029t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0019c0019t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0020c0024t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0021c0023t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0022c0021t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0023c0020t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0024c0022t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
a0025c0027t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0005 | c0006 | t0003 | g0086 | EUR | GBR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0149 | EUR | GBR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00423 | hp1 | a0004 | c0004 | t0002 | g0094 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00438 | hp2 | a0006 | c0005 | t0002 | g0104 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00558 | hp1 | a0004 | c0004 | t0002 | g0097 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00609 | hp1 | a0008 | c0008 | t0001 | g0119 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00609 | hp2 | a0004 | c0004 | t0002 | g0027 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00621 | hp1 | a0010 | c0010 | t0001 | g0183 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0156 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00735 | hp2 | a0008 | c0008 | t0001 | g0205 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0103 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00741 | hp1 | a0005 | c0006 | t0003 | g0081 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG00741 | hp2 | a0003 | c0003 | t0014 | g0079 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01070 | hp2 | a0007 | c0007 | t0004 | g0228 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01071 | hp1 | a0011 | c0011 | t0003 | g0118 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01071 | hp2 | a0007 | c0007 | t0004 | g0219 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01074 | hp2 | a0010 | c0010 | t0001 | g0171 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01081 | hp1 | a0005 | c0006 | t0003 | g0218 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0151 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01106 | hp1 | a0008 | c0008 | t0001 | g0207 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01109 | hp1 | a0007 | c0007 | t0004 | g0090 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01109 | hp2 | a0006 | c0005 | t0006 | g0221 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0160 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01167 | hp2 | a0005 | c0006 | t0003 | g0291 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01169 | hp1 | a0005 | c0006 | t0003 | g0227 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01169 | hp2 | a0003 | c0003 | t0001 | g0179 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0269 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0029 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01192 | hp2 | a0012 | c0012 | t0004 | g0140 | AMR | PUR | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01256 | hp1 | a0006 | c0005 | t0001 | g0170 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01256 | hp2 | a0007 | c0007 | t0004 | g0001 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01258 | hp2 | a0007 | c0007 | t0004 | g0001 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01261 | hp1 | a0007 | c0007 | t0004 | g0231 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01358 | hp1 | a0006 | c0005 | t0011 | g0145 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01433 | hp1 | a0011 | c0011 | t0003 | g0112 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01433 | hp2 | a0005 | c0006 | t0003 | g0202 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01496 | hp2 | a0010 | c0010 | t0001 | g0105 | AMR | CLM | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0126 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0142 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01517 | hp2 | a0007 | c0007 | t0004 | g0198 | EUR | IBS | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01884 | hp2 | a0015 | c0017 | t0001 | g0293 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01928 | hp2 | a0008 | c0008 | t0001 | g0209 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01952 | hp2 | a0003 | c0003 | t0001 | g0022 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01975 | hp1 | a0012 | c0012 | t0004 | g0162 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01978 | hp1 | a0005 | c0006 | t0003 | g0080 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01978 | hp2 | a0003 | c0003 | t0001 | g0210 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01993 | hp1 | a0005 | c0006 | t0003 | g0266 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG01993 | hp2 | a0003 | c0003 | t0001 | g0152 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02015 | hp1 | a0016 | c0025 | t0001 | g0082 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02027 | hp2 | a0004 | c0004 | t0002 | g0054 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02071 | hp1 | a0017 | c0028 | t0001 | g0116 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02074 | hp2 | a0018 | c0029 | t0001 | g0131 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02083 | hp2 | a0006 | c0005 | t0002 | g0264 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02129 | hp2 | a0004 | c0004 | t0002 | g0114 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0100 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02148 | hp2 | a0008 | c0008 | t0001 | g0135 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02257 | hp1 | a0002 | c0002 | t0005 | g0076 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02273 | hp1 | a0010 | c0010 | t0001 | g0299 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02280 | hp1 | a0009 | c0009 | t0007 | g0254 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0238 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02300 | hp1 | a0005 | c0006 | t0003 | g0159 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02300 | hp2 | a0012 | c0012 | t0004 | g0161 | AMR | PEL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02523 | hp2 | a0004 | c0004 | t0002 | g0072 | EAS | KHV | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02602 | hp1 | a0003 | c0003 | t0008 | g0133 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0260 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02622 | hp2 | a0007 | c0007 | t0004 | g0244 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02698 | hp2 | a0006 | c0005 | t0001 | g0139 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0290 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02735 | hp2 | a0011 | c0011 | t0003 | g0124 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02895 | hp2 | a0007 | c0007 | t0004 | g0242 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02897 | hp2 | a0007 | c0007 | t0004 | g0243 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02922 | hp2 | a0003 | c0015 | t0001 | g0013 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02965 | hp1 | a0003 | c0003 | t0006 | g0005 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03017 | hp1 | a0012 | c0012 | t0004 | g0144 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03041 | hp1 | a0009 | c0009 | t0001 | g0253 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03041 | hp2 | a0007 | c0007 | t0004 | g0241 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0075 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03098 | hp2 | a0001 | c0016 | t0005 | g0015 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03130 | hp1 | a0001 | c0018 | t0001 | g0102 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03130 | hp2 | a0009 | c0009 | t0001 | g0258 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0083 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03453 | hp2 | a0002 | c0002 | t0013 | g0007 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03486 | hp2 | a0001 | c0026 | t0001 | g0251 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03516 | hp1 | a0001 | c0016 | t0005 | g0014 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ESN | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03540 | hp1 | a0007 | c0007 | t0004 | g0008 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03540 | hp2 | a0007 | c0007 | t0004 | g0058 | AFR | GWD | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03704 | hp1 | a0001 | c0001 | t0012 | g0204 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03704 | hp2 | a0011 | c0011 | t0003 | g0122 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03710 | hp1 | a0006 | c0005 | t0008 | g0087 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03710 | hp2 | a0005 | c0006 | t0003 | g0281 | SAS | PJL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03831 | hp1 | a0019 | c0019 | t0003 | g0109 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0285 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0172 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG04115 | hp1 | a0011 | c0011 | t0003 | g0125 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG04184 | hp1 | a0005 | c0006 | t0001 | g0208 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG04199 | hp1 | a0003 | c0003 | t0008 | g0177 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18522 | hp1 | a0002 | c0002 | t0007 | g0255 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18522 | hp2 | a0001 | c0018 | t0001 | g0262 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0245 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18941 | hp1 | a0005 | c0006 | t0003 | g0032 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18944 | hp1 | a0004 | c0004 | t0002 | g0036 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18946 | hp2 | a0020 | c0024 | t0001 | g0132 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18947 | hp1 | a0013 | c0013 | t0001 | g0193 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18947 | hp2 | a0004 | c0004 | t0002 | g0071 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18948 | hp1 | a0021 | c0023 | t0001 | g0127 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18953 | hp2 | a0008 | c0008 | t0001 | g0123 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18954 | hp2 | a0013 | c0013 | t0001 | g0194 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18957 | hp2 | a0009 | c0009 | t0001 | g0113 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18960 | hp1 | a0010 | c0010 | t0001 | g0201 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18960 | hp2 | a0009 | c0009 | t0001 | g0166 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18962 | hp1 | a0008 | c0008 | t0001 | g0168 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18962 | hp2 | a0009 | c0009 | t0001 | g0064 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18965 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18965 | hp2 | a0006 | c0005 | t0002 | g0096 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18966 | hp2 | a0004 | c0004 | t0002 | g0235 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18969 | hp1 | a0006 | c0005 | t0001 | g0115 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18969 | hp2 | a0014 | c0014 | t0001 | g0040 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18971 | hp1 | a0010 | c0010 | t0001 | g0278 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18974 | hp1 | a0004 | c0004 | t0002 | g0175 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18974 | hp2 | a0008 | c0008 | t0001 | g0197 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18975 | hp1 | a0008 | c0008 | t0001 | g0214 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18975 | hp2 | a0004 | c0004 | t0002 | g0240 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18977 | hp1 | a0013 | c0013 | t0001 | g0181 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18979 | hp1 | a0003 | c0003 | t0002 | g0167 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18982 | hp2 | a0022 | c0021 | t0002 | g0098 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18983 | hp1 | a0004 | c0004 | t0002 | g0025 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18983 | hp2 | a0023 | c0020 | t0001 | g0039 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18987 | hp1 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18989 | hp1 | a0006 | c0005 | t0001 | g0037 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18990 | hp2 | a0008 | c0008 | t0001 | g0215 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18993 | hp1 | a0006 | c0005 | t0002 | g0089 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18993 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18995 | hp1 | a0004 | c0004 | t0001 | g0233 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18995 | hp2 | a0004 | c0004 | t0002 | g0024 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18999 | hp1 | a0006 | c0005 | t0002 | g0200 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18999 | hp2 | a0014 | c0014 | t0001 | g0038 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19000 | hp2 | a0004 | c0004 | t0002 | g0165 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19003 | hp1 | a0009 | c0009 | t0001 | g0111 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19004 | hp1 | a0014 | c0014 | t0001 | g0049 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19004 | hp2 | a0004 | c0004 | t0002 | g0128 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19009 | hp2 | a0009 | c0009 | t0001 | g0101 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19010 | hp2 | a0006 | c0005 | t0001 | g0117 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19012 | hp2 | a0009 | c0009 | t0001 | g0092 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19043 | hp2 | a0015 | c0017 | t0001 | g0292 | AFR | LWK | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19056 | hp2 | a0009 | c0009 | t0001 | g0099 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19057 | hp1 | a0004 | c0004 | t0002 | g0033 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19057 | hp2 | a0003 | c0003 | t0001 | g0234 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19062 | hp2 | a0010 | c0010 | t0001 | g0028 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19063 | hp2 | a0013 | c0013 | t0001 | g0192 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19065 | hp2 | a0004 | c0004 | t0002 | g0073 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19077 | hp1 | a0024 | c0022 | t0001 | g0050 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19240 | hp1 | a0025 | c0027 | t0001 | g0060 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ASW | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA20129 | hp2 | a0002 | c0002 | t0007 | g0056 | AFR | ASW | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA20752 | hp1 | a0006 | c0005 | t0001 | g0154 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA20752 | hp2 | a0011 | c0011 | t0003 | g0212 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA20805 | hp1 | a0010 | c0010 | t0001 | g0199 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA20805 | hp2 | a0005 | c0006 | t0003 | g0106 | EUR | TSI | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02559 | hp1 | a0003 | c0015 | t0001 | g0012 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG02559 | hp2 | a0012 | c0012 | t0004 | g0229 | AFR | ACB | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03471 | hp1 | a0003 | c0003 | t0006 | g0006 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | MSL | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | USA | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18955 | hp1 | a0008 | c0008 | t0001 | g0077 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
NA18955 | hp2 | a0004 | c0004 | t0002 | g0088 | EAS | JPT | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
homoSapiens | chm13v2 | a0005 | c0006 | t0003 | g0300 | REF | REF | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0250 | REF | REF | IMPG1_chr6_75916114_76077662 | IMPG1 | chr6 | 75916114 | 76077662 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75922106 | C | T | 4 | a0008 a0010 a0016 others(1): Show |
21 | HG00609.hp1 HG00621.hp1 HG00735.hp2 others(18): Show |
missense_variant | MODERATE | c.2377G>A | p.Asp793Asn | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 2551/3543 | 2377/2394 | 793/797 | chr6 | 75922106 | |||
chr6:75923668 | C | T | 3 | a0005 a0011 a0019 |
20 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(17): Show |
missense_variant | MODERATE | c.2282G>A | p.Ser761Asn | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/17 | 2456/3543 | 2282/2394 | 761/797 | chr6 | 75923668 | |||
chr6:75931064 | C | T | 5 | a0003 a0004 a0006 others(2): Show |
72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
missense_variant | MODERATE | c.2132G>A | p.Arg711His | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/17 | 2306/3543 | 2132/2394 | 711/797 | chr6 | 75931064 | |||
chr6:75931086 | G | A | 2 | a0007 a0012 |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
missense_variant | MODERATE | c.2110C>T | p.Arg704Trp | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/17 | 2284/3543 | 2110/2394 | 704/797 | chr6 | 75931086 | |||
chr6:75950680 | T | C | 5 | a0004 a0009 a0014 others(2): Show |
34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
missense_variant | MODERATE | c.1706A>G | p.Lys569Arg | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1880/3543 | 1706/2394 | 569/797 | chr6 | 75950680 | |||
chr6:75950834 | G | C | 13 | a0001 a0003 a0004 others(10): Show |
197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
missense_variant | MODERATE | c.1552C>G | p.His518Asp | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1726/3543 | 1552/2394 | 518/797 | chr6 | 75950834 | |||
chr6:75950998 | C | A | 1 | a0025 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1388G>T | p.Gly463Val | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1562/3543 | 1388/2394 | 463/797 | chr6 | 75950998 | |||
chr6:75951069 | C | T | 1 | a0015 | 2 | HG01884.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1317G>A | p.Met439Ile | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1491/3543 | 1317/2394 | 439/797 | chr6 | 75951069 | |||
chr6:76002938 | C | T | 3 | a0020 a0021 a0024 |
3 | NA18946.hp2 NA18948.hp1 NA19077.hp1 |
missense_variant | MODERATE | c.1271G>A | p.Gly424Glu | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/17 | 1445/3543 | 1271/2394 | 424/797 | chr6 | 76002938 | |||
chr6:76002969 | G | A | 1 | a0017 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1240C>T | p.Pro414Ser | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/17 | 1414/3543 | 1240/2394 | 414/797 | chr6 | 76002969 | |||
chr6:76005322 | T | C | 1 | a0013 | 4 | NA18947.hp1 NA18954.hp2 NA18977.hp1 others(1): Show |
missense_variant | MODERATE | c.1100A>G | p.Gln367Arg | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/17 | 1274/3543 | 1100/2394 | 367/797 | chr6 | 76005322 | |||
chr6:76018807 | C | T | 3 | a0014 a0022 a0023 |
5 | NA18969.hp2 NA18982.hp2 NA18983.hp2 others(2): Show |
missense_variant | MODERATE | c.718G>A | p.Val240Ile | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/17 | 892/3543 | 718/2394 | 240/797 | chr6 | 76018807 | |||
chr6:76022132 | G | A | 1 | a0018 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.650C>T | p.Thr217Ile | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/17 | 824/3543 | 650/2394 | 217/797 | chr6 | 76022132 | |||
chr6:76042021 | C | T | 1 | a0019 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.173G>A | p.Arg58Lys | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/17 | 347/3543 | 173/2394 | 58/797 | chr6 | 76042021 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75947402 | A | T | 1 | a0001c0018 | 2 | HG03130.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1956T>A | p.Ala652Ala | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/17 | 2130/3543 | 1956/2394 | 652/797 | chr6 | 75947402 | |||
chr6:75950973 | G | A | 1 | a0001c0026 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1413C>T | p.Asp471Asp | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/17 | 1587/3543 | 1413/2394 | 471/797 | chr6 | 75950973 | |||
chr6:76025216 | A | C | 2 | a0001c0016 a0003c0015 |
4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.540T>G | p.Gly180Gly | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/17 | 714/3543 | 540/2394 | 180/797 | chr6 | 76025216 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75921185 | G | GAGAT | 3 | a0001c0001t0005 a0001c0016t0005 a0002c0002t0005 |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*900_*903dupATCT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 903 | chr6 | 75921185 | ||||||
chr6:75921224 | A | G | 1 | a0002c0002t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 865 | chr6 | 75921224 | ||||||
chr6:75921279 | T | C | 1 | a0006c0005t0011 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 810 | chr6 | 75921279 | ||||||
chr6:75921450 | G | T | 2 | a0003c0003t0008 a0006c0005t0008 |
3 | HG02602.hp1 HG03710.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 639 | chr6 | 75921450 | ||||||
chr6:75921530 | C | T | 1 | a0001c0001t0010 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*559G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 559 | chr6 | 75921530 | ||||||
chr6:75921543 | T | A | 1 | a0001c0001t0012 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 546 | chr6 | 75921543 | ||||||
chr6:75921572 | T | C | 1 | a0002c0002t0013 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 517 | chr6 | 75921572 | ||||||
chr6:75921666 | C | T | 1 | a0001c0001t0009 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 423 | chr6 | 75921666 | ||||||
chr6:75921700 | A | G | 2 | a0007c0007t0004 a0012c0012t0004 |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*389T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 389 | chr6 | 75921700 | ||||||
chr6:75921758 | C | T | 3 | a0005c0006t0003 a0011c0011t0003 a0019c0019t0003 |
19 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 331 | chr6 | 75921758 | ||||||
chr6:75921800 | G | A | 1 | a0003c0003t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 289 | chr6 | 75921800 | ||||||
chr6:75921875 | GGTTT | G | 4 | a0003c0003t0002 a0004c0004t0002 a0006c0005t0002 others(1): Show |
25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*210_*213delAAAC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 210 | chr6 | 75921875 | ||||||
chr6:75921888 | A | G | 2 | a0002c0002t0007 a0009c0009t0007 |
3 | HG02280.hp1 NA18522.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 201 | chr6 | 75921888 | ||||||
chr6:75921978 | A | G | 2 | a0003c0003t0006 a0006c0005t0006 |
3 | HG01109.hp2 HG02965.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 17/17 | 111 | chr6 | 75921978 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75922244 | A | G | 3 | a0001c0001t0001g0042 a0009c0009t0001g0099 a0017c0028t0001g0116 |
3 | HG02071.hp1 NA19003.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2317-78T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922244 | |||||||
chr6:75922309 | A | G | 2 | a0007c0007t0004g0219 a0007c0007t0004g0228 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2317-143T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922309 | |||||||
chr6:75922353 | C | T | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2317-187G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922353 | |||||||
chr6:75922630 | T | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(38): Show |
42 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2317-464A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922630 | |||||||
chr6:75922662 | G | A | 1 | a0003c0003t0006g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2317-496C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922662 | |||||||
chr6:75922903 | A | AT | 10 | a0001c0018t0001g0102 a0002c0002t0001g0226 a0003c0003t0001g0149 others(7): Show |
10 | HG00140.hp2 HG00741.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2316+730dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75922903 | |||||||
chr6:75923102 | TGTAAAAT others(12): Show |
T | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2316+513_2316+531d others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923102 | |||||||
chr6:75923288 | G | C | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2316+346C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923288 | |||||||
chr6:75923406 | A | G | 1 | a0002c0002t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2316+228T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923406 | |||||||
chr6:75923418 | A | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(76): Show |
81 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.2316+216T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923418 | |||||||
chr6:75923487 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2316+147T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 16/16 | chr6 | 75923487 | |||||||
chr6:75923826 | T | C | 1 | a0002c0002t0001g0289 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2244-120A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75923826 | |||||||
chr6:75923841 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0009c0009t0001g0253 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-135G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75923841 | |||||||
chr6:75923893 | T | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0110 others(5): Show |
8 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244-187A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75923893 | |||||||
chr6:75924103 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2244-397A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924103 | |||||||
chr6:75924242 | TATCTATC others(213): Show |
T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-756_2244-537d others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924242 | |||||||
chr6:75924444 | AATATAAC others(6): Show |
A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0009c0009t0001g0253 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-751_2244-739d others(15): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924444 | |||||||
chr6:75924451 | C | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0018t0001g0262 others(3): Show |
6 | HG02723.hp2 HG02896.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-745G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924451 | |||||||
chr6:75924451 | CAT | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(19): Show |
22 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2244-747_2244-746d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924451 | |||||||
chr6:75924468 | A | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-762T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924468 | |||||||
chr6:75924481 | A | G | 1 | a0011c0011t0003g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2244-775T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924481 | |||||||
chr6:75924482 | T | A | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-776A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924482 | |||||||
chr6:75924488 | TATA | T | 9 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0110 others(6): Show |
9 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2244-785_2244-783d others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924488 | |||||||
chr6:75924499 | T | C | 5 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2244-793A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924499 | |||||||
chr6:75924500 | A | ATATAATA others(20): Show |
12 | a0007c0007t0004g0001 a0007c0007t0004g0008 a0007c0007t0004g0058 others(9): Show |
13 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2244-821_2244-795d others(29): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924500 | |||||||
chr6:75924504 | A | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-798T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924504 | |||||||
chr6:75924508 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(59): Show |
63 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.2244-802A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924508 | |||||||
chr6:75924509 | A | G | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-803T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924509 | |||||||
chr6:75924513 | A | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-807T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924513 | |||||||
chr6:75924527 | T | A | 2 | a0004c0004t0002g0097 a0004c0004t0002g0165 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2244-821A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924527 | |||||||
chr6:75924527 | TTATAATA others(6): Show |
T | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-834_2244-822d others(15): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924527 | |||||||
chr6:75924528 | TATAATAT others(178): Show |
T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-1007_2244-823 others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924528 | |||||||
chr6:75924529 | A | ATAATATA others(15): Show |
4 | a0002c0002t0001g0136 a0009c0009t0001g0064 a0009c0009t0001g0101 others(1): Show |
4 | NA18962.hp2 NA18977.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-845_2244-824d others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924529 | |||||||
chr6:75924530 | TA | T | 69 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0003c0003t0001g0016 others(66): Show |
69 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2244-825delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924530 | |||||||
chr6:75924531 | A | AATTAATA others(14): Show |
2 | a0003c0003t0001g0044 a0003c0003t0001g0045 |
2 | NA18959.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2244-826_2244-825i others(23): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924531 | |||||||
chr6:75924544 | A | AATATAAT others(19): Show |
2 | a0007c0007t0004g0219 a0007c0007t0004g0228 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2244-839_2244-838i others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924544 | |||||||
chr6:75924544 | A | AATATAAT others(19): Show |
1 | a0001c0001t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2244-864_2244-839d others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924544 | |||||||
chr6:75924550 | A | T | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-844T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924550 | |||||||
chr6:75924552 | TA | T | 3 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0014c0014t0001g0049 |
3 | NA18985.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2244-847delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924552 | |||||||
chr6:75924554 | A | AT | 82 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(79): Show |
82 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2244-849dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924554 | |||||||
chr6:75924557 | TA | T | 4 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0002c0002t0001g0148 others(1): Show |
4 | HG01175.hp2 NA18985.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-852delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924557 | |||||||
chr6:75924558 | A | AT | 82 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(79): Show |
82 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2244-853_2244-852i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924558 | |||||||
chr6:75924558 | A | C | 1 | a0004c0004t0002g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2244-852T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924558 | |||||||
chr6:75924561 | T | A | 86 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(83): Show |
86 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2244-855A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924561 | |||||||
chr6:75924566 | ATTAT | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(17): Show |
20 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2244-864_2244-861d others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924566 | |||||||
chr6:75924568 | T | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(253): Show |
258 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.2244-862A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924568 | |||||||
chr6:75924568 | T | TATATATA others(32): Show |
2 | a0004c0004t0002g0097 a0004c0004t0002g0165 |
2 | HG00558.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2244-863_2244-862i others(41): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924568 | |||||||
chr6:75924569 | ATATATAA others(1): Show |
A | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-871_2244-864d others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924569 | |||||||
chr6:75924571 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0263 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2244-865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924571 | |||||||
chr6:75924575 | AAT | A | 86 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(83): Show |
86 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2244-871_2244-870d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924575 | |||||||
chr6:75924578 | T | A | 2 | a0002c0002t0001g0065 a0002c0002t0001g0268 |
2 | HG01074.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2244-872A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924578 | |||||||
chr6:75924579 | A | T | 2 | a0002c0002t0001g0065 a0002c0002t0001g0268 |
2 | HG01074.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2244-873T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924579 | |||||||
chr6:75924583 | TA | T | 86 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(83): Show |
86 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2244-878delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924583 | |||||||
chr6:75924593 | T | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0007c0007t0004g0241 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-887A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924593 | |||||||
chr6:75924593 | TTA | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(55): Show |
59 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.2244-889_2244-888d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924593 | |||||||
chr6:75924594 | T | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(17): Show |
20 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2244-888A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924594 | |||||||
chr6:75924595 | A | ATATAATT others(29): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2244-890_2244-889i others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924595 | |||||||
chr6:75924598 | T | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0007c0007t0004g0241 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-892A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924598 | |||||||
chr6:75924599 | A | T | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0007c0007t0004g0241 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-893T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924599 | |||||||
chr6:75924601 | A | G | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-895T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924601 | |||||||
chr6:75924603 | T | TA | 6 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0007c0007t0004g0241 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244-898_2244-897i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924603 | |||||||
chr6:75924603 | T | TTAATA | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-898_2244-897i others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924603 | |||||||
chr6:75924604 | T | A | 4 | a0002c0002t0013g0007 a0003c0003t0001g0156 a0003c0003t0001g0160 others(1): Show |
4 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-898A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924604 | |||||||
chr6:75924605 | A | AT | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
89 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2244-900_2244-899i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924605 | |||||||
chr6:75924605 | A | T | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-899T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924605 | |||||||
chr6:75924608 | T | G | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-902A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924608 | |||||||
chr6:75924615 | A | C | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-909T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924615 | |||||||
chr6:75924615 | A | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(16): Show |
19 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2244-909T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924615 | |||||||
chr6:75924622 | A | G | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-916T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924622 | |||||||
chr6:75924624 | TAAATTA | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(89): Show |
92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-924_2244-919d others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924624 | |||||||
chr6:75924625 | A | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(21): Show |
24 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2244-919T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924625 | |||||||
chr6:75924629 | T | TATATATA others(2): Show |
3 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 |
3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-924_2244-923i others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924629 | |||||||
chr6:75924636 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2244-930A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924636 | |||||||
chr6:75924636 | T | C | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-930A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924636 | |||||||
chr6:75924636 | T | G | 92 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(89): Show |
92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-930A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924636 | |||||||
chr6:75924637 | A | T | 1 | a0004c0004t0002g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2244-931T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924637 | |||||||
chr6:75924643 | A | C | 92 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(89): Show |
92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-937T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924643 | |||||||
chr6:75924643 | A | G | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-937T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924643 | |||||||
chr6:75924645 | T | TA | 93 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(90): Show |
93 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.2244-940_2244-939i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924645 | |||||||
chr6:75924645 | T | TATA | 3 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 |
3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-940_2244-939i others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924645 | |||||||
chr6:75924646 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2244-940A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924646 | |||||||
chr6:75924647 | A | AT | 3 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 |
3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-942_2244-941i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924647 | |||||||
chr6:75924647 | A | T | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-941T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924647 | |||||||
chr6:75924654 | T | TAC | 13 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(10): Show |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-949_2244-948i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924654 | |||||||
chr6:75924656 | T | TCA | 3 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 |
3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-951_2244-950i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924656 | |||||||
chr6:75924657 | A | ATG | 66 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(63): Show |
66 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.2244-952_2244-951i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | |||||||
chr6:75924657 | A | ATGATATA others(2): Show |
3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2244-952_2244-951i others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | |||||||
chr6:75924657 | A | G | 15 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(12): Show |
15 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2244-951T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | |||||||
chr6:75924657 | A | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(110): Show |
113 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.2244-951T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924657 | |||||||
chr6:75924658 | A | T | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-952T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924658 | |||||||
chr6:75924659 | T | C | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-953A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924659 | |||||||
chr6:75924664 | A | AAT | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-960_2244-959d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | |||||||
chr6:75924664 | A | AATAT | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2244-959_2244-958i others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | |||||||
chr6:75924664 | A | AATTATAT others(1): Show |
3 | a0007c0007t0004g0008 a0007c0007t0004g0090 a0012c0012t0004g0229 |
3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2244-959_2244-958i others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | |||||||
chr6:75924664 | A | C | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-958T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | |||||||
chr6:75924664 | A | G | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0110 others(7): Show |
10 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-958T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | |||||||
chr6:75924664 | A | T | 81 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(78): Show |
81 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2244-958T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924664 | |||||||
chr6:75924667 | A | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-961T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924667 | |||||||
chr6:75924668 | A | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(261): Show |
266 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.2244-962T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924668 | |||||||
chr6:75924669 | A | T | 1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-963T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924669 | |||||||
chr6:75924670 | T | A | 93 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(90): Show |
93 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.2244-964A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924670 | |||||||
chr6:75924670 | T | TAATA | 64 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(61): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2244-965_2244-964i others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924670 | |||||||
chr6:75924670 | T | TTA | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-966_2244-965d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924670 | |||||||
chr6:75924671 | T | A | 27 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(24): Show |
28 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.2244-965A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | |||||||
chr6:75924671 | T | C | 6 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 others(3): Show |
6 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-965A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | |||||||
chr6:75924671 | T | TATATATA | 67 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(64): Show |
68 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.2244-966_2244-965i others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | |||||||
chr6:75924671 | TA | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(89): Show |
92 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2244-966delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924671 | |||||||
chr6:75924673 | T | A | 1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-967A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924673 | |||||||
chr6:75924675 | T | TA | 6 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 others(3): Show |
6 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-970dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924675 | |||||||
chr6:75924678 | T | A | 4 | a0001c0001t0010g0003 a0002c0002t0013g0007 a0003c0003t0001g0178 others(1): Show |
4 | HG01261.hp1 HG02015.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-972A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924678 | |||||||
chr6:75924678 | T | C | 12 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0110 others(9): Show |
12 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2244-972A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924678 | |||||||
chr6:75924678 | T | G | 125 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(122): Show |
125 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2244-972A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924678 | |||||||
chr6:75924682 | T | TATAATTA | 3 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0006c0005t0011g0145 |
3 | HG01358.hp1 NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-977_2244-976i others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924682 | |||||||
chr6:75924684 | T | A | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2244-978A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924684 | |||||||
chr6:75924684 | T | TCA | 39 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(36): Show |
39 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.2244-979_2244-978i others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924684 | |||||||
chr6:75924685 | T | A | 3 | a0003c0003t0001g0156 a0003c0003t0001g0160 a0003c0003t0001g0179 |
3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2244-979A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924685 | |||||||
chr6:75924685 | T | C | 118 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(115): Show |
118 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.2244-979A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924685 | |||||||
chr6:75924685 | T | G | 1 | a0001c0001t0010g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2244-979A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924685 | |||||||
chr6:75924689 | TATAAATA | T | 13 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(10): Show |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-990_2244-984d others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924689 | |||||||
chr6:75924690 | ATAAATAA others(6): Show |
A | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-997_2244-985d others(15): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924690 | |||||||
chr6:75924690 | ATAAATAA others(8): Show |
A | 82 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(79): Show |
82 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2244-999_2244-985d others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924690 | |||||||
chr6:75924691 | T | A | 10 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0002c0002t0001g0065 others(7): Show |
10 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-985A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924691 | |||||||
chr6:75924691 | T | TC | 7 | a0002c0002t0001g0136 a0003c0003t0001g0156 a0003c0003t0001g0160 others(4): Show |
7 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244-986_2244-985i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924691 | |||||||
chr6:75924692 | A | AT | 28 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0003c0003t0002g0167 others(25): Show |
28 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.2244-987_2244-986i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924692 | |||||||
chr6:75924692 | A | T | 10 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0002c0002t0001g0065 others(7): Show |
10 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-986T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924692 | |||||||
chr6:75924693 | A | AT | 4 | a0001c0018t0001g0262 a0007c0007t0004g0008 a0007c0007t0004g0090 others(1): Show |
4 | HG01109.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244-988_2244-987i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | |||||||
chr6:75924693 | A | ATATATCA others(1): Show |
42 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(39): Show |
42 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.2244-988_2244-987i others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | |||||||
chr6:75924693 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0274 a0006c0005t0011g0145 |
3 | HG01358.hp1 NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-987T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | |||||||
chr6:75924693 | A | T | 17 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0002c0002t0001g0065 others(14): Show |
17 | HG00735.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2244-987T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924693 | |||||||
chr6:75924694 | A | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(106): Show |
111 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2244-988T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924694 | |||||||
chr6:75924695 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2244-989A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924695 | |||||||
chr6:75924695 | TA | T | 10 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0002c0002t0001g0065 others(7): Show |
10 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244-990delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924695 | |||||||
chr6:75924696 | A | AT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(108): Show |
112 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2244-991_2244-990i others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924696 | |||||||
chr6:75924696 | A | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(15): Show |
18 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244-990T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924696 | |||||||
chr6:75924697 | AT | A | 4 | a0002c0002t0001g0136 a0009c0009t0001g0064 a0009c0009t0001g0101 others(1): Show |
4 | NA18962.hp2 NA18977.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-992delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924697 | |||||||
chr6:75924698 | T | A | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-992A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924698 | |||||||
chr6:75924699 | T | A | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-993A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924699 | |||||||
chr6:75924699 | T | C | 38 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(35): Show |
38 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2244-993A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924699 | |||||||
chr6:75924699 | T | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-993A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924699 | |||||||
chr6:75924701 | T | TATGATAT others(3): Show |
3 | a0007c0007t0004g0008 a0007c0007t0004g0090 a0012c0012t0004g0229 |
3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2244-996_2244-995i others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924701 | |||||||
chr6:75924703 | T | TA | 25 | a0003c0003t0002g0167 a0004c0004t0002g0024 a0004c0004t0002g0025 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2244-998dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924703 | |||||||
chr6:75924705 | T | A | 13 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(10): Show |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-999A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924705 | |||||||
chr6:75924706 | A | AATATATA others(8): Show |
2 | a0003c0003t0001g0191 a0004c0004t0001g0233 |
2 | NA18957.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2244-1001_2244-100 others(19): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | |||||||
chr6:75924706 | A | AATATATC others(7): Show |
1 | a0002c0002t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2244-1001_2244-100 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | |||||||
chr6:75924706 | A | AATATATC others(8): Show |
37 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(34): Show |
37 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2244-1001_2244-100 others(19): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | |||||||
chr6:75924706 | A | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.2244-1000T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924706 | |||||||
chr6:75924707 | A | AT | 3 | a0007c0007t0004g0008 a0007c0007t0004g0090 a0012c0012t0004g0229 |
3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2244-1002dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924707 | |||||||
chr6:75924707 | A | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(80): Show |
83 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.2244-1001T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924707 | |||||||
chr6:75924708 | T | C | 1 | a0001c0001t0010g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2244-1002A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924708 | |||||||
chr6:75924710 | T | TA | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2244-1005dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924710 | |||||||
chr6:75924711 | ATAATAT | A | 6 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0002c0002t0001g0065 others(3): Show |
6 | HG01074.hp1 HG01175.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-1011_2244-100 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924711 | |||||||
chr6:75924713 | A | AATTATAT others(1): Show |
9 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(6): Show |
9 | HG01433.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | AATTATAT others(17): Show |
1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-1008_2244-100 others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | AATTATAT others(16): Show |
37 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(34): Show |
38 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(27): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | AATTATAT others(65): Show |
13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0084 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(76): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | AATTATAT others(63): Show |
26 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0257 others(23): Show |
27 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(74): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | AATTATAT others(57): Show |
6 | a0005c0006t0003g0080 a0005c0006t0003g0081 a0005c0006t0003g0086 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-1008_2244-100 others(68): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2244-1007T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0274 |
2 | NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-1007T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924713 | A | T | 127 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(124): Show |
127 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.2244-1007T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924713 | |||||||
chr6:75924717 | T | TA | 10 | a0001c0018t0001g0262 a0003c0003t0001g0075 a0003c0003t0001g0156 others(7): Show |
10 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-1012dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924717 | |||||||
chr6:75924719 | T | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.2244-1013A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924719 | |||||||
chr6:75924720 | A | C | 51 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(48): Show |
51 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.2244-1014T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924720 | |||||||
chr6:75924720 | A | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(31): Show |
34 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2244-1014T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924720 | |||||||
chr6:75924720 | AATATAAT others(29): Show |
A | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2244-1050_2244-101 others(40): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924720 | |||||||
chr6:75924724 | TA | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(33): Show |
36 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2244-1019delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924724 | |||||||
chr6:75924725 | A | AATTATAT | 79 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(76): Show |
79 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.2244-1026_2244-102 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924725 | |||||||
chr6:75924727 | T | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0274 |
2 | NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2244-1021A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924727 | |||||||
chr6:75924728 | T | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(22): Show |
25 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2244-1022A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | |||||||
chr6:75924728 | T | TATATATA | 58 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(55): Show |
59 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.2244-1029_2244-102 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | |||||||
chr6:75924728 | T | TATATATA others(7): Show |
1 | a0007c0007t0004g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2244-1036_2244-102 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | |||||||
chr6:75924728 | TATATATA others(7): Show |
T | 13 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(10): Show |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2244-1036_2244-102 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924728 | |||||||
chr6:75924735 | A | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(15): Show |
18 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244-1029T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924735 | |||||||
chr6:75924735 | A | T | 35 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(32): Show |
35 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2244-1029T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924735 | |||||||
chr6:75924737 | T | TATATA | 3 | a0005c0006t0001g0208 a0005c0006t0003g0281 a0011c0011t0003g0122 |
3 | HG03704.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2244-1036_2244-103 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924737 | |||||||
chr6:75924739 | T | TA | 10 | a0003c0003t0001g0075 a0003c0003t0001g0156 a0003c0003t0001g0160 others(7): Show |
10 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-1034dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924739 | |||||||
chr6:75924741 | T | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(15): Show |
18 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244-1035A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924741 | |||||||
chr6:75924742 | A | AATATAAT others(1): Show |
65 | a0002c0002t0001g0136 a0003c0003t0001g0016 a0003c0003t0001g0022 others(62): Show |
65 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2244-1037_2244-103 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924742 | |||||||
chr6:75924742 | A | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(27): Show |
30 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2244-1036T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924742 | |||||||
chr6:75924742 | AATATATA others(7): Show |
A | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-1050_2244-103 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924742 | |||||||
chr6:75924743 | A | ATATAAT | 9 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(6): Show |
9 | HG01433.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2244-1038_2244-103 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924743 | |||||||
chr6:75924749 | A | G | 9 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(6): Show |
9 | HG01433.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2244-1043T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924749 | |||||||
chr6:75924756 | C | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(235): Show |
240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.2244-1050G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | |||||||
chr6:75924756 | C | CATATAAT others(37): Show |
32 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(29): Show |
32 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.2244-1051_2244-105 others(48): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | |||||||
chr6:75924756 | C | CATATAAT others(59): Show |
1 | a0006c0005t0011g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2244-1051_2244-105 others(70): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | |||||||
chr6:75924756 | C | CATATAAT others(51): Show |
7 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(4): Show |
7 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2244-1051_2244-105 others(62): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | |||||||
chr6:75924756 | C | CATATAAT others(71): Show |
1 | a0002c0002t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2244-1051_2244-105 others(82): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | |||||||
chr6:75924756 | C | CATATAAT others(58): Show |
1 | a0011c0011t0003g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2244-1051_2244-105 others(69): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924756 | |||||||
chr6:75924763 | T | A | 1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-1057A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924763 | |||||||
chr6:75924774 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2244-1068T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75924774 | |||||||
chr6:75925162 | C | T | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244-1456G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925162 | |||||||
chr6:75925208 | A | G | 3 | a0005c0006t0001g0208 a0005c0006t0003g0281 a0011c0011t0003g0122 |
3 | HG03704.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2244-1502T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925208 | |||||||
chr6:75925247 | CAGTT | C | 71 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(68): Show |
71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2244-1545_2244-154 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925247 | |||||||
chr6:75925494 | T | A | 1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-1788A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925494 | |||||||
chr6:75925624 | C | T | 3 | a0002c0002t0001g0296 a0002c0002t0001g0297 a0009c0009t0001g0166 |
3 | NA18945.hp1 NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2244-1918G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925624 | |||||||
chr6:75925669 | A | ATTTG | 8 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(5): Show |
8 | HG02257.hp1 HG02615.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2244-1967_2244-196 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925669 | |||||||
chr6:75925669 | A | ATTTGTTT others(1): Show |
189 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(186): Show |
189 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.2244-1971_2244-196 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925669 | |||||||
chr6:75925805 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(76): Show |
81 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.2244-2099T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925805 | |||||||
chr6:75925822 | C | T | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2244-2116G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925822 | |||||||
chr6:75925861 | T | C | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-2155A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925861 | |||||||
chr6:75925890 | T | A | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-2184A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925890 | |||||||
chr6:75925897 | C | T | 1 | a0005c0006t0003g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2244-2191G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75925897 | |||||||
chr6:75926026 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(76): Show |
81 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.2244-2320G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926026 | |||||||
chr6:75926200 | G | A | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(282): Show |
287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.2244-2494C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926200 | |||||||
chr6:75926305 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2244-2599G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926305 | |||||||
chr6:75926434 | G | A | 1 | a0004c0004t0002g0235 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2244-2728C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926434 | |||||||
chr6:75926667 | T | C | 88 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(85): Show |
88 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2244-2961A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926667 | |||||||
chr6:75926706 | A | T | 1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-3000T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926706 | |||||||
chr6:75926707 | T | A | 1 | a0002c0002t0001g0296 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2244-3001A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926707 | |||||||
chr6:75926713 | C | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2244-3007G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926713 | |||||||
chr6:75926728 | C | CA | 68 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(65): Show |
68 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2244-3023dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926728 | |||||||
chr6:75926790 | C | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2244-3084G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926790 | |||||||
chr6:75926814 | GGAGTA | G | 72 | a0001c0018t0001g0262 a0003c0003t0001g0016 a0003c0003t0001g0022 others(69): Show |
72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2244-3113_2244-310 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926814 | |||||||
chr6:75926962 | C | T | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244-3256G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926962 | |||||||
chr6:75926973 | C | T | 2 | a0004c0004t0002g0094 a0006c0005t0002g0264 |
2 | HG00423.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.2244-3267G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75926973 | |||||||
chr6:75927085 | G | GA | 6 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244-3380dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927085 | |||||||
chr6:75927401 | T | C | 17 | a0007c0007t0004g0001 a0007c0007t0004g0008 a0007c0007t0004g0058 others(14): Show |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2243+3552A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927401 | |||||||
chr6:75927427 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2243+3526T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927427 | |||||||
chr6:75927680 | C | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2243+3273G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927680 | |||||||
chr6:75927715 | T | TTCCC | 4 | a0001c0018t0001g0102 a0002c0002t0001g0297 a0009c0009t0001g0113 others(1): Show |
4 | HG03130.hp1 NA18945.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2243+3234_2243+323 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927715 | |||||||
chr6:75927731 | C | T | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2243+3222G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927731 | |||||||
chr6:75927789 | T | G | 25 | a0003c0003t0002g0167 a0004c0004t0002g0024 a0004c0004t0002g0025 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2243+3164A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927789 | |||||||
chr6:75927790 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
39 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2243+3163C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927790 | |||||||
chr6:75927807 | C | CAAAAATG others(4778): Show |
1 | a0013c0013t0001g0181 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2243+3145_2243+314 others(4789): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927807 | C | CAAAAATG others(4775): Show |
2 | a0001c0001t0001g0095 a0002c0002t0001g0068 |
2 | HG00673.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4786): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927807 | C | CAAAAATG others(4776): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0203 others(2): Show |
5 | HG00621.hp2 HG02027.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4787): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927807 | C | CAAAAATG others(4777): Show |
9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG00438.hp1 NA18941.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4788): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927807 | C | CAAAAATG others(4778): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0130 others(1): Show |
4 | HG00597.hp1 HG01928.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.2243+3145_2243+314 others(4789): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927807 | C | CAAAAATG others(4777): Show |
1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2243+3145_2243+314 others(4788): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927807 | C | CAAAAATG others(4779): Show |
1 | a0001c0001t0001g0176 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2243+3145_2243+314 others(4790): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927807 | |||||||
chr6:75927842 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2243+3111G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927842 | |||||||
chr6:75927843 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0002c0002t0001g0068 |
3 | HG00673.hp1 HG02129.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2243+3110C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927843 | |||||||
chr6:75927852 | T | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2243+3101A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927852 | |||||||
chr6:75927907 | G | A | 5 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243+3046C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927907 | |||||||
chr6:75927981 | T | C | 1 | a0004c0004t0002g0114 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2243+2972A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75927981 | |||||||
chr6:75928104 | A | G | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
89 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.2243+2849T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928104 | |||||||
chr6:75928207 | C | CT | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+2745dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928207 | |||||||
chr6:75928211 | T | C | 2 | a0006c0005t0002g0089 a0006c0005t0002g0096 |
2 | NA18965.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2243+2742A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928211 | |||||||
chr6:75928239 | G | A | 1 | a0001c0001t0005g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2243+2714C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928239 | |||||||
chr6:75928308 | T | G | 2 | a0007c0007t0004g0008 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2243+2645A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928308 | |||||||
chr6:75928410 | G | A | 17 | a0007c0007t0004g0001 a0007c0007t0004g0008 a0007c0007t0004g0058 others(14): Show |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2243+2543C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928410 | |||||||
chr6:75928419 | C | A | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2243+2534G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928419 | |||||||
chr6:75928481 | C | T | 2 | a0002c0002t0007g0056 a0002c0002t0007g0255 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2243+2472G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928481 | |||||||
chr6:75928567 | A | C | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2243+2386T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928567 | |||||||
chr6:75928601 | T | A | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+2352A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928601 | |||||||
chr6:75928859 | A | G | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2243+2094T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928859 | |||||||
chr6:75928895 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(59): Show |
63 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.2243+2058T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928895 | |||||||
chr6:75928939 | C | A | 1 | a0011c0011t0003g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2243+2014G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75928939 | |||||||
chr6:75929011 | A | G | 165 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(162): Show |
165 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.2243+1942T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929011 | |||||||
chr6:75929166 | A | G | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+1787T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929166 | |||||||
chr6:75929167 | T | TAATG | 17 | a0007c0007t0004g0001 a0007c0007t0004g0008 a0007c0007t0004g0058 others(14): Show |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2243+1782_2243+178 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929167 | |||||||
chr6:75929233 | T | A | 110 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(107): Show |
110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2243+1720A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929233 | |||||||
chr6:75929385 | T | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+1568A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929385 | |||||||
chr6:75929455 | A | G | 1 | a0005c0006t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2243+1498T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929455 | |||||||
chr6:75929536 | C | G | 3 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0014c0014t0001g0049 |
3 | NA18985.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2243+1417G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929536 | |||||||
chr6:75929603 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(28): Show |
31 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2243+1350C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929603 | |||||||
chr6:75929739 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2243+1214T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929739 | |||||||
chr6:75929748 | G | T | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(282): Show |
287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.2243+1205C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929748 | |||||||
chr6:75929754 | TA | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(22): Show |
25 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2243+1198delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929754 | |||||||
chr6:75929996 | G | C | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2243+957C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75929996 | |||||||
chr6:75930054 | C | A | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2243+899G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930054 | |||||||
chr6:75930071 | C | T | 2 | a0002c0002t0007g0056 a0002c0002t0007g0255 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2243+882G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930071 | |||||||
chr6:75930138 | C | G | 31 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(28): Show |
31 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2243+815G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930138 | |||||||
chr6:75930504 | C | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+449G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930504 | |||||||
chr6:75930535 | G | A | 1 | a0006c0005t0001g0037 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2243+418C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930535 | |||||||
chr6:75930641 | G | A | 7 | a0002c0002t0001g0252 a0002c0002t0001g0261 a0002c0002t0007g0056 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2243+312C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930641 | |||||||
chr6:75930658 | T | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2243+295A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930658 | |||||||
chr6:75930679 | G | A | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+274C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930679 | |||||||
chr6:75930833 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2243+120T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930833 | |||||||
chr6:75930883 | C | G | 3 | a0004c0004t0002g0071 a0004c0004t0002g0128 a0022c0021t0002g0098 |
3 | NA18947.hp2 NA18982.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2243+70G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 15/16 | chr6 | 75930883 | |||||||
chr6:75931177 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.2045-26G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931177 | |||||||
chr6:75931244 | A | G | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2045-93T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931244 | |||||||
chr6:75931311 | T | C | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045-160A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931311 | |||||||
chr6:75931393 | A | C | 9 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045-242T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931393 | |||||||
chr6:75931426 | C | A | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-275G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931426 | |||||||
chr6:75931579 | GT | G | 74 | a0001c0018t0001g0262 a0002c0002t0013g0007 a0003c0003t0001g0016 others(71): Show |
74 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2045-429delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931579 | |||||||
chr6:75931625 | T | G | 3 | a0013c0013t0001g0192 a0013c0013t0001g0193 a0013c0013t0001g0194 |
3 | NA18947.hp1 NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2045-474A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931625 | |||||||
chr6:75931706 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0010g0003 others(1): Show |
4 | HG00673.hp1 HG02129.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2045-555C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931706 | |||||||
chr6:75931964 | T | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-813A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75931964 | |||||||
chr6:75932213 | G | C | 13 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(10): Show |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-1062C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932213 | |||||||
chr6:75932244 | G | A | 19 | a0005c0006t0001g0208 a0005c0006t0003g0032 a0005c0006t0003g0080 others(16): Show |
19 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2045-1093C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932244 | |||||||
chr6:75932288 | C | T | 1 | a0011c0011t0003g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2045-1137G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932288 | |||||||
chr6:75932289 | T | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(57): Show |
61 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.2045-1138A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932289 | |||||||
chr6:75932301 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2045-1150G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932301 | |||||||
chr6:75932413 | G | T | 1 | a0002c0002t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2045-1262C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932413 | |||||||
chr6:75932567 | A | C | 5 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045-1416T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932567 | |||||||
chr6:75932756 | A | C | 1 | a0006c0005t0011g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2045-1605T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932756 | |||||||
chr6:75932770 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2045-1619T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932770 | |||||||
chr6:75932809 | T | C | 1 | a0005c0006t0003g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2045-1658A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932809 | |||||||
chr6:75932815 | C | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-1664G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932815 | |||||||
chr6:75932820 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(73): Show |
78 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2045-1669G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932820 | |||||||
chr6:75932906 | G | T | 8 | a0007c0007t0004g0001 a0007c0007t0004g0058 a0007c0007t0004g0198 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2045-1755C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75932906 | |||||||
chr6:75933033 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2045-1882T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933033 | |||||||
chr6:75933169 | A | G | 1 | a0004c0004t0002g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2045-2018T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933169 | |||||||
chr6:75933186 | C | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-2035G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933186 | |||||||
chr6:75933193 | A | G | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2045-2042T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933193 | |||||||
chr6:75933337 | A | G | 1 | a0009c0009t0001g0101 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2045-2186T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933337 | |||||||
chr6:75933364 | G | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-2213C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933364 | |||||||
chr6:75933411 | A | T | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2045-2260T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933411 | |||||||
chr6:75933450 | A | G | 44 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(41): Show |
44 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.2045-2299T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933450 | |||||||
chr6:75933657 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
39 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2045-2506T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933657 | |||||||
chr6:75933681 | C | T | 1 | a0003c0003t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2045-2530G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933681 | |||||||
chr6:75933725 | A | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-2574T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933725 | |||||||
chr6:75933839 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2045-2688G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933839 | |||||||
chr6:75933864 | T | G | 1 | a0005c0006t0003g0081 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2045-2713A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933864 | |||||||
chr6:75933885 | A | G | 2 | a0001c0001t0001g0009 a0002c0002t0013g0007 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-2734T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933885 | |||||||
chr6:75933925 | G | A | 18 | a0005c0006t0001g0208 a0005c0006t0003g0032 a0005c0006t0003g0080 others(15): Show |
18 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2045-2774C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933925 | |||||||
chr6:75933926 | G | A | 1 | a0006c0005t0002g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2045-2775C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75933926 | |||||||
chr6:75934021 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2045-2870A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934021 | |||||||
chr6:75934139 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0271 |
2 | NA18959.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2045-2988C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934139 | |||||||
chr6:75934144 | C | A | 8 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0110 others(5): Show |
8 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2045-2993G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934144 | |||||||
chr6:75934166 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2045-3015T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934166 | |||||||
chr6:75934315 | C | A | 1 | a0002c0002t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2045-3164G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934315 | |||||||
chr6:75934416 | G | A | 25 | a0003c0003t0002g0167 a0004c0004t0002g0024 a0004c0004t0002g0025 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2045-3265C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934416 | |||||||
chr6:75934512 | T | C | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2045-3361A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934512 | |||||||
chr6:75934554 | C | T | 2 | a0001c0001t0012g0204 a0002c0002t0001g0169 |
2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2045-3403G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934554 | |||||||
chr6:75934577 | T | G | 13 | a0001c0001t0005g0010 a0001c0001t0005g0017 a0001c0001t0005g0018 others(10): Show |
13 | HG02257.hp1 HG02293.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2045-3426A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934577 | |||||||
chr6:75934631 | A | G | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-3480T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934631 | |||||||
chr6:75934662 | T | G | 1 | a0009c0009t0001g0092 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2045-3511A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934662 | |||||||
chr6:75934668 | C | T | 71 | a0001c0001t0001g0009 a0002c0002t0013g0007 a0003c0003t0001g0016 others(68): Show |
71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2045-3517G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934668 | |||||||
chr6:75934691 | A | C | 2 | a0005c0006t0003g0081 a0005c0006t0003g0086 |
2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2045-3540T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934691 | |||||||
chr6:75934720 | C | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2045-3569G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934720 | |||||||
chr6:75934795 | C | G | 2 | a0001c0018t0001g0102 a0001c0018t0001g0262 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2045-3644G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934795 | |||||||
chr6:75934810 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(57): Show |
61 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.2045-3659G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934810 | |||||||
chr6:75934868 | C | T | 2 | a0001c0001t0001g0009 a0002c0002t0013g0007 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-3717G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934868 | |||||||
chr6:75934999 | A | C | 1 | a0010c0010t0001g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2045-3848T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75934999 | |||||||
chr6:75935291 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2045-4140G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935291 | |||||||
chr6:75935443 | A | G | 1 | a0005c0006t0003g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2045-4292T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935443 | |||||||
chr6:75935492 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2045-4341G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935492 | |||||||
chr6:75935691 | C | T | 2 | a0001c0001t0001g0009 a0002c0002t0013g0007 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-4540G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935691 | |||||||
chr6:75935837 | G | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2045-4686C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75935837 | |||||||
chr6:75936086 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(60): Show |
64 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2045-4935G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936086 | |||||||
chr6:75936106 | C | G | 2 | a0001c0018t0001g0102 a0001c0018t0001g0262 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2045-4955G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936106 | |||||||
chr6:75936117 | C | T | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2045-4966G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936117 | |||||||
chr6:75936140 | AT | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0295 a0021c0023t0001g0127 |
3 | HG00597.hp1 NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2045-4990delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936140 | |||||||
chr6:75936241 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2045-5090T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936241 | |||||||
chr6:75936368 | T | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(68): Show |
72 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2045-5217A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936368 | |||||||
chr6:75936518 | A | T | 1 | a0011c0011t0003g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2045-5367T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936518 | |||||||
chr6:75936762 | G | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(60): Show |
64 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2045-5611C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936762 | |||||||
chr6:75936823 | T | C | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2045-5672A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936823 | |||||||
chr6:75936941 | G | A | 1 | a0002c0002t0001g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2045-5790C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936941 | |||||||
chr6:75936944 | A | G | 2 | a0001c0001t0001g0009 a0002c0002t0013g0007 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-5793T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936944 | |||||||
chr6:75936954 | A | G | 5 | a0008c0008t0001g0135 a0008c0008t0001g0205 a0008c0008t0001g0207 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045-5803T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75936954 | |||||||
chr6:75937054 | G | A | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2045-5903C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937054 | |||||||
chr6:75937099 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2045-5948C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937099 | |||||||
chr6:75937323 | G | A | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-6172C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937323 | |||||||
chr6:75937391 | T | C | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2045-6240A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937391 | |||||||
chr6:75937469 | GGC | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(38): Show |
42 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2045-6320_2045-631 others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937469 | |||||||
chr6:75937483 | G | A | 88 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0070 others(85): Show |
88 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2045-6332C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937483 | |||||||
chr6:75937504 | G | A | 1 | a0001c0001t0005g0223 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2045-6353C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937504 | |||||||
chr6:75937597 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2045-6446G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937597 | |||||||
chr6:75937644 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(41): Show |
45 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2045-6493A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937644 | |||||||
chr6:75937672 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2045-6521T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937672 | |||||||
chr6:75937693 | A | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(60): Show |
64 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2045-6542T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937693 | |||||||
chr6:75937800 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0010g0003 |
3 | HG00673.hp1 NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2045-6649C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937800 | |||||||
chr6:75937859 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(156): Show |
161 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2045-6708G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937859 | |||||||
chr6:75937890 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(156): Show |
161 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2045-6739A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937890 | |||||||
chr6:75937927 | A | T | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2045-6776T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937927 | |||||||
chr6:75937991 | G | A | 68 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0029 others(65): Show |
68 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2045-6840C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937991 | |||||||
chr6:75937999 | T | C | 3 | a0007c0007t0004g0008 a0007c0007t0004g0090 a0012c0012t0004g0229 |
3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2045-6848A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75937999 | |||||||
chr6:75938001 | G | A | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2045-6850C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938001 | |||||||
chr6:75938365 | C | A | 2 | a0009c0009t0001g0064 a0013c0013t0001g0181 |
2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2045-7214G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938365 | |||||||
chr6:75938366 | C | G | 2 | a0009c0009t0001g0064 a0013c0013t0001g0181 |
2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2045-7215G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938366 | |||||||
chr6:75938469 | A | G | 3 | a0007c0007t0004g0008 a0007c0007t0004g0090 a0012c0012t0004g0229 |
3 | HG01109.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2045-7318T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938469 | |||||||
chr6:75938523 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2045-7372G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938523 | |||||||
chr6:75938573 | G | A | 10 | a0002c0002t0005g0076 a0007c0007t0004g0001 a0007c0007t0004g0058 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-7422C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938573 | |||||||
chr6:75938695 | A | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(282): Show |
287 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.2045-7544T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938695 | |||||||
chr6:75938730 | T | C | 2 | a0002c0002t0001g0195 a0002c0002t0001g0211 |
2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2045-7579A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938730 | |||||||
chr6:75938744 | C | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2045-7593G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938744 | |||||||
chr6:75938810 | T | TCAAAA | 153 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0042 others(150): Show |
154 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.2045-7664_2045-766 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | |||||||
chr6:75938810 | T | TCAAAACA others(3): Show |
82 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(79): Show |
83 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2045-7669_2045-766 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | |||||||
chr6:75938810 | T | TCAAAACA others(8): Show |
1 | a0001c0001t0001g0274 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2045-7674_2045-766 others(19): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | |||||||
chr6:75938810 | T | TCAAAACA others(13): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0061 |
3 | HG03209.hp2 HG03579.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2045-7679_2045-766 others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | |||||||
chr6:75938810 | TCAAAA | T | 27 | a0001c0018t0001g0262 a0003c0003t0001g0075 a0003c0003t0002g0167 others(24): Show |
27 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2045-7664_2045-766 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938810 | |||||||
chr6:75938831 | CAAAACAA others(13): Show |
C | 5 | a0007c0007t0004g0231 a0007c0007t0004g0241 a0007c0007t0004g0242 others(2): Show |
5 | HG01261.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045-7700_2045-768 others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938831 | |||||||
chr6:75938851 | A | C | 8 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(5): Show |
8 | HG01109.hp1 HG02293.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2045-7700T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938851 | |||||||
chr6:75938887 | C | T | 1 | a0002c0002t0001g0285 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2045-7736G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938887 | |||||||
chr6:75938912 | C | T | 10 | a0002c0002t0005g0076 a0007c0007t0004g0001 a0007c0007t0004g0058 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-7761G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938912 | |||||||
chr6:75938923 | T | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2045-7772A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938923 | |||||||
chr6:75938981 | G | A | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-7830C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75938981 | |||||||
chr6:75939082 | A | C | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2045-7931T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939082 | |||||||
chr6:75939109 | G | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2045-7958C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939109 | |||||||
chr6:75939119 | G | A | 10 | a0002c0002t0005g0076 a0007c0007t0004g0001 a0007c0007t0004g0058 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-7968C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939119 | |||||||
chr6:75939209 | A | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2045-8058T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939209 | |||||||
chr6:75939247 | G | A | 1 | a0002c0002t0001g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2044+8067C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939247 | |||||||
chr6:75939350 | T | TC | 27 | a0003c0003t0001g0232 a0003c0003t0002g0167 a0004c0004t0002g0024 others(24): Show |
27 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2044+7963dupG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939350 | |||||||
chr6:75939355 | C | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(106): Show |
109 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.2044+7959G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939355 | |||||||
chr6:75939355 | C | T | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044+7959G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939355 | |||||||
chr6:75939841 | G | C | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2044+7473C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939841 | |||||||
chr6:75939888 | C | T | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2044+7426G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75939888 | |||||||
chr6:75940193 | C | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(67): Show |
71 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2044+7121G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940193 | |||||||
chr6:75940331 | A | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0002c0002t0001g0146 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2044+6983T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940331 | |||||||
chr6:75940342 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2044+6972A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940342 | |||||||
chr6:75940436 | C | T | 4 | a0004c0004t0002g0071 a0004c0004t0002g0128 a0004c0004t0002g0240 others(1): Show |
4 | NA18947.hp2 NA18975.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044+6878G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940436 | |||||||
chr6:75940494 | T | C | 10 | a0002c0002t0005g0076 a0007c0007t0004g0001 a0007c0007t0004g0058 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044+6820A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940494 | |||||||
chr6:75940602 | T | G | 10 | a0003c0003t0001g0100 a0003c0003t0001g0186 a0003c0003t0001g0232 others(7): Show |
10 | HG01256.hp1 HG01358.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.2044+6712A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940602 | |||||||
chr6:75940744 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(38): Show |
42 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2044+6570T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940744 | |||||||
chr6:75940759 | C | T | 2 | a0001c0018t0001g0102 a0001c0018t0001g0262 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+6555G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940759 | |||||||
chr6:75940760 | G | A | 72 | a0001c0001t0001g0257 a0003c0003t0001g0016 a0003c0003t0001g0022 others(69): Show |
72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2044+6554C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940760 | |||||||
chr6:75940767 | T | G | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2044+6547A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940767 | |||||||
chr6:75940964 | T | G | 7 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(4): Show |
7 | HG02615.hp2 HG03098.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044+6350A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75940964 | |||||||
chr6:75941117 | T | TG | 89 | a0001c0001t0001g0009 a0001c0001t0001g0257 a0001c0001t0005g0017 others(86): Show |
90 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2044+6196dupC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941117 | |||||||
chr6:75941124 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2044+6190C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941124 | |||||||
chr6:75941169 | G | A | 2 | a0001c0001t0001g0009 a0002c0002t0013g0007 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2044+6145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941169 | |||||||
chr6:75941196 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(18): Show |
21 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2044+6118A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941196 | |||||||
chr6:75941361 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2044+5953C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941361 | |||||||
chr6:75941550 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2044+5764G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941550 | |||||||
chr6:75941629 | T | G | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2044+5685A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941629 | |||||||
chr6:75941660 | ACT | A | 3 | a0003c0003t0001g0075 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2044+5652_2044+565 others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941660 | |||||||
chr6:75941688 | G | A | 1 | a0005c0006t0003g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2044+5626C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941688 | |||||||
chr6:75941736 | C | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(69): Show |
73 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2044+5578G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941736 | |||||||
chr6:75941938 | G | A | 286 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(283): Show |
288 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.2044+5376C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941938 | |||||||
chr6:75941981 | C | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(246): Show |
251 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.2044+5333G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75941981 | |||||||
chr6:75942046 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2044+5268G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942046 | |||||||
chr6:75942110 | T | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0009c0009t0001g0253 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044+5204A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942110 | |||||||
chr6:75942145 | C | T | 3 | a0010c0010t0001g0105 a0010c0010t0001g0171 a0010c0010t0001g0199 |
3 | HG01074.hp2 HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2044+5169G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942145 | |||||||
chr6:75942175 | A | G | 1 | a0011c0011t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2044+5139T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942175 | |||||||
chr6:75942494 | G | C | 3 | a0001c0001t0001g0053 a0002c0002t0001g0048 a0014c0014t0001g0049 |
3 | NA18985.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2044+4820C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942494 | |||||||
chr6:75942546 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(152): Show |
157 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.2044+4768G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942546 | |||||||
chr6:75942594 | T | C | 18 | a0005c0006t0001g0208 a0005c0006t0003g0032 a0005c0006t0003g0080 others(15): Show |
18 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2044+4720A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942594 | |||||||
chr6:75942726 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(41): Show |
45 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2044+4588G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942726 | |||||||
chr6:75942781 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2044+4533C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942781 | |||||||
chr6:75942836 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2044+4478T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75942836 | |||||||
chr6:75943119 | G | A | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044+4195C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943119 | |||||||
chr6:75943138 | G | C | 1 | a0007c0007t0004g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2044+4176C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943138 | |||||||
chr6:75943204 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(159): Show |
164 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2044+4110G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943204 | |||||||
chr6:75943278 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2044+4036A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943278 | |||||||
chr6:75943284 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0003c0003t0001g0075 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+4030T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943284 | |||||||
chr6:75943378 | G | A | 88 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0070 others(85): Show |
88 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2044+3936C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943378 | |||||||
chr6:75943628 | A | C | 2 | a0001c0018t0001g0102 a0001c0018t0001g0262 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+3686T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943628 | |||||||
chr6:75943990 | C | T | 2 | a0001c0001t0001g0009 a0002c0002t0013g0007 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2044+3324G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75943990 | |||||||
chr6:75944136 | C | T | 10 | a0002c0002t0005g0076 a0007c0007t0004g0001 a0007c0007t0004g0058 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044+3178G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944136 | |||||||
chr6:75944137 | G | A | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2044+3177C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944137 | |||||||
chr6:75944255 | C | T | 2 | a0001c0018t0001g0102 a0001c0018t0001g0262 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+3059G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944255 | |||||||
chr6:75944302 | C | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(19): Show |
22 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2044+3012G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944302 | |||||||
chr6:75944693 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2044+2621G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944693 | |||||||
chr6:75944705 | T | A | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2044+2609A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944705 | |||||||
chr6:75944915 | CTT | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(239): Show |
244 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.2044+2397_2044+239 others(6): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75944915 | |||||||
chr6:75945037 | A | C | 1 | a0001c0001t0001g0284 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2044+2277T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945037 | |||||||
chr6:75945208 | G | A | 3 | a0003c0003t0006g0005 a0003c0003t0006g0006 a0006c0005t0006g0221 |
3 | HG01109.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2044+2106C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945208 | |||||||
chr6:75945253 | G | A | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2044+2061C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945253 | |||||||
chr6:75945358 | C | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+1956G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945358 | |||||||
chr6:75945358 | CT | C | 43 | a0001c0001t0001g0271 a0003c0003t0001g0016 a0003c0003t0001g0029 others(40): Show |
43 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2044+1955delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945358 | |||||||
chr6:75945359 | T | C | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+1955A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945359 | |||||||
chr6:75945552 | T | A | 24 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0027 others(21): Show |
24 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2044+1762A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945552 | |||||||
chr6:75945722 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0270 a0001c0001t0001g0273 others(6): Show |
9 | HG01081.hp2 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2044+1592C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945722 | |||||||
chr6:75945882 | G | T | 10 | a0002c0002t0005g0076 a0007c0007t0004g0001 a0007c0007t0004g0058 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044+1432C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945882 | |||||||
chr6:75945989 | G | A | 2 | a0001c0018t0001g0102 a0001c0018t0001g0262 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2044+1325C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75945989 | |||||||
chr6:75946055 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(46): Show |
50 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2044+1259A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946055 | |||||||
chr6:75946253 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2044+1061C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946253 | |||||||
chr6:75946604 | A | G | 8 | a0007c0007t0004g0008 a0007c0007t0004g0090 a0007c0007t0004g0231 others(5): Show |
8 | HG01109.hp1 HG01261.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2044+710T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946604 | |||||||
chr6:75946877 | AT | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(18): Show |
21 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2044+436delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946877 | |||||||
chr6:75946974 | C | T | 1 | a0003c0003t0001g0191 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2044+340G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946974 | |||||||
chr6:75946994 | T | G | 2 | a0002c0002t0001g0146 a0002c0002t0001g0147 |
2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2044+320A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75946994 | |||||||
chr6:75947023 | T | C | 172 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0055 others(169): Show |
173 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.2044+291A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947023 | |||||||
chr6:75947098 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2044+216C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947098 | |||||||
chr6:75947148 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2044+166G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947148 | |||||||
chr6:75947261 | AT | A | 171 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0055 others(168): Show |
171 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.2044+52delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 14/16 | chr6 | 75947261 | |||||||
chr6:75947646 | T | G | 1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1825-113A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947646 | |||||||
chr6:75947747 | G | T | 30 | a0003c0003t0001g0016 a0003c0003t0001g0022 a0003c0003t0001g0083 others(27): Show |
30 | HG00140.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1825-214C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947747 | |||||||
chr6:75947825 | A | G | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-292T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947825 | |||||||
chr6:75947857 | TA | T | 131 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(128): Show |
132 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1825-325delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947857 | |||||||
chr6:75947857 | TAA | T | 6 | a0007c0007t0004g0231 a0007c0007t0004g0241 a0007c0007t0004g0242 others(3): Show |
6 | HG01261.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-326_1825-325d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947857 | |||||||
chr6:75947871 | C | A | 17 | a0005c0006t0001g0208 a0005c0006t0003g0080 a0005c0006t0003g0081 others(14): Show |
17 | HG00140.hp1 HG00741.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1825-338G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947871 | |||||||
chr6:75947981 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(200): Show |
205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.1825-448G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75947981 | |||||||
chr6:75948182 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG02896.hp1 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825-649A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948182 | |||||||
chr6:75948251 | T | C | 4 | a0001c0018t0001g0262 a0002c0002t0001g0230 a0002c0002t0005g0076 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-718A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948251 | |||||||
chr6:75948355 | GGCTCTGA others(2): Show |
G | 7 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(4): Show |
7 | HG02615.hp2 HG02922.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825-831_1825-823d others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948355 | |||||||
chr6:75948369 | GC | G | 8 | a0001c0001t0001g0009 a0002c0002t0013g0007 a0007c0007t0004g0008 others(5): Show |
8 | HG01261.hp1 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-837delG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948369 | |||||||
chr6:75948536 | G | T | 43 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0001g0174 others(40): Show |
43 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1825-1003C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948536 | |||||||
chr6:75948700 | G | A | 2 | a0002c0002t0001g0252 a0002c0002t0001g0261 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1825-1167C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948700 | |||||||
chr6:75948876 | C | T | 1 | a0005c0006t0003g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1825-1343G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948876 | |||||||
chr6:75948909 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1825-1376A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948909 | |||||||
chr6:75948941 | G | A | 1 | a0006c0005t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1825-1408C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75948941 | |||||||
chr6:75949001 | A | G | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1825-1468T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949001 | |||||||
chr6:75949101 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0225 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+1461T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949101 | |||||||
chr6:75949438 | A | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(8): Show |
11 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1824+1124T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949438 | |||||||
chr6:75949660 | C | T | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1824+902G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949660 | |||||||
chr6:75949733 | ATGGTG | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0003c0003t0001g0083 |
3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1824+824_1824+828d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949733 | |||||||
chr6:75949798 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1824+764A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949798 | |||||||
chr6:75949844 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1824+718C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75949844 | |||||||
chr6:75950102 | T | C | 1 | a0003c0003t0001g0191 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1824+460A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950102 | |||||||
chr6:75950123 | G | T | 2 | a0012c0012t0004g0161 a0012c0012t0004g0162 |
2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1824+439C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950123 | |||||||
chr6:75950139 | C | G | 3 | a0001c0026t0001g0251 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1824+423G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950139 | |||||||
chr6:75950247 | T | C | 1 | a0025c0027t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1824+315A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950247 | |||||||
chr6:75950417 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1824+145G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950417 | |||||||
chr6:75950418 | T | C | 31 | a0004c0004t0001g0233 a0004c0004t0002g0024 a0004c0004t0002g0025 others(28): Show |
31 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1824+144A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950418 | |||||||
chr6:75950465 | A | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0225 others(3): Show |
6 | HG01261.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+97T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950465 | |||||||
chr6:75950554 | C | T | 6 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(3): Show |
6 | HG01070.hp1 HG01433.hp1 HG01516.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1824+8G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 13/16 | chr6 | 75950554 | |||||||
chr6:75951223 | A | AT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(77): Show |
82 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1292-130dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951223 | |||||||
chr6:75951223 | AT | A | 74 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(71): Show |
74 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1292-130delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951223 | |||||||
chr6:75951236 | T | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-142A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951236 | |||||||
chr6:75951590 | G | GA | 45 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(42): Show |
46 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1292-497dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951590 | |||||||
chr6:75951635 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(165): Show |
170 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1292-541C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951635 | |||||||
chr6:75951684 | T | G | 76 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-590A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951684 | |||||||
chr6:75951796 | G | C | 1 | a0002c0002t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1292-702C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951796 | |||||||
chr6:75951814 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0225 others(3): Show |
6 | HG01261.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-720G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951814 | |||||||
chr6:75951872 | G | A | 3 | a0001c0001t0001g0257 a0001c0018t0001g0262 a0007c0007t0004g0008 |
3 | HG03540.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-778C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951872 | |||||||
chr6:75951891 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
163 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1292-797C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951891 | |||||||
chr6:75951914 | C | T | 76 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-820G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951914 | |||||||
chr6:75951943 | AAAT | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(288): Show |
293 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(290): Show |
intron_variant | MODIFIER | c.1292-852_1292-850d others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951943 | |||||||
chr6:75951960 | A | C | 2 | a0004c0004t0002g0114 a0009c0009t0001g0113 |
2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1292-866T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75951960 | |||||||
chr6:75952004 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-910G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952004 | |||||||
chr6:75952062 | C | T | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1292-968G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952062 | |||||||
chr6:75952177 | C | A | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-1083G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952177 | |||||||
chr6:75952341 | G | C | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-1247C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952341 | |||||||
chr6:75952365 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1292-1271G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952365 | |||||||
chr6:75952453 | C | A | 1 | a0004c0004t0002g0235 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1292-1359G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952453 | |||||||
chr6:75952630 | G | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-1536C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952630 | |||||||
chr6:75952675 | A | G | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-1581T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952675 | |||||||
chr6:75952764 | G | A | 2 | a0002c0002t0001g0136 a0007c0007t0004g0231 |
2 | HG01261.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1292-1670C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75952764 | |||||||
chr6:75953062 | T | A | 149 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(146): Show |
150 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1292-1968A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953062 | |||||||
chr6:75953069 | T | TTCTTATG others(6): Show |
4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-1988_1292-197 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953069 | |||||||
chr6:75953095 | C | T | 1 | a0002c0002t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1292-2001G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953095 | |||||||
chr6:75953096 | G | A | 76 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-2002C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953096 | |||||||
chr6:75953781 | A | G | 145 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(142): Show |
146 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1292-2687T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953781 | |||||||
chr6:75953909 | A | C | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-2815T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953909 | |||||||
chr6:75953937 | T | C | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1292-2843A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75953937 | |||||||
chr6:75954094 | G | T | 34 | a0004c0004t0001g0233 a0004c0004t0002g0024 a0004c0004t0002g0025 others(31): Show |
34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1292-3000C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954094 | |||||||
chr6:75954183 | G | A | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-3089C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954183 | |||||||
chr6:75954229 | A | G | 29 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(26): Show |
30 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-3135T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954229 | |||||||
chr6:75954260 | C | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0263 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1292-3166G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954260 | |||||||
chr6:75954281 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
162 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1292-3187A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954281 | |||||||
chr6:75954323 | T | C | 1 | a0007c0007t0004g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1292-3229A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954323 | |||||||
chr6:75954398 | G | A | 1 | a0001c0001t0009g0260 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1292-3304C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954398 | |||||||
chr6:75954420 | A | C | 17 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(14): Show |
17 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1292-3326T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954420 | |||||||
chr6:75954438 | T | C | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-3344A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954438 | |||||||
chr6:75954623 | T | C | 11 | a0002c0002t0001g0068 a0002c0002t0001g0093 a0002c0002t0001g0134 others(8): Show |
11 | HG01261.hp2 HG01496.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-3529A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954623 | |||||||
chr6:75954913 | A | T | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1292-3819T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75954913 | |||||||
chr6:75955317 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1292-4223C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955317 | |||||||
chr6:75955406 | T | G | 2 | a0001c0001t0001g0190 a0010c0010t0001g0183 |
2 | HG00621.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1292-4312A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955406 | |||||||
chr6:75955869 | T | A | 34 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(31): Show |
35 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1292-4775A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955869 | |||||||
chr6:75955919 | T | C | 1 | a0002c0002t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1292-4825A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75955919 | |||||||
chr6:75956004 | G | A | 1 | a0011c0011t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1292-4910C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956004 | |||||||
chr6:75956106 | C | T | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-5012G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956106 | |||||||
chr6:75956146 | T | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(26): Show |
30 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-5052A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956146 | |||||||
chr6:75956203 | T | C | 2 | a0002c0002t0001g0147 a0002c0002t0005g0076 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1292-5109A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956203 | |||||||
chr6:75956248 | T | A | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-5154A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956248 | |||||||
chr6:75956489 | T | C | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1292-5395A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956489 | |||||||
chr6:75956510 | G | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(26): Show |
30 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-5416C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956510 | |||||||
chr6:75956584 | C | T | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-5490G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956584 | |||||||
chr6:75956725 | C | A | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-5631G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956725 | |||||||
chr6:75956951 | G | A | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-5857C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956951 | |||||||
chr6:75956964 | A | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-5870T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75956964 | |||||||
chr6:75957119 | C | T | 45 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(42): Show |
46 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1292-6025G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957119 | |||||||
chr6:75957217 | C | T | 45 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(42): Show |
46 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1292-6123G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957217 | |||||||
chr6:75957252 | G | T | 1 | a0003c0003t0001g0151 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1292-6158C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957252 | |||||||
chr6:75957435 | C | G | 1 | a0003c0003t0001g0269 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1292-6341G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957435 | |||||||
chr6:75957480 | T | C | 1 | a0019c0019t0003g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1292-6386A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957480 | |||||||
chr6:75957548 | C | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(26): Show |
30 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1292-6454G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957548 | |||||||
chr6:75957948 | A | T | 76 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-6854T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75957948 | |||||||
chr6:75958034 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-6940G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958034 | |||||||
chr6:75958058 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-6964G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958058 | |||||||
chr6:75958618 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-7524A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958618 | |||||||
chr6:75958716 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(11): Show |
14 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-7622C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958716 | |||||||
chr6:75958854 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1292-7760G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958854 | |||||||
chr6:75958932 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.1292-7838G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75958932 | |||||||
chr6:75959062 | G | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-7968C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959062 | |||||||
chr6:75959088 | A | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
162 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1292-7994T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959088 | |||||||
chr6:75959475 | C | G | 76 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(73): Show |
76 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-8381G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959475 | |||||||
chr6:75959485 | G | T | 1 | a0002c0002t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1292-8391C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959485 | |||||||
chr6:75959684 | A | C | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1292-8590T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959684 | |||||||
chr6:75959761 | A | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18986.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1292-8667T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959761 | |||||||
chr6:75959789 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1292-8695C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959789 | |||||||
chr6:75959954 | G | A | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1292-8860C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959954 | |||||||
chr6:75959978 | C | G | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-8884G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75959978 | |||||||
chr6:75960125 | C | T | 2 | a0005c0006t0003g0080 a0005c0006t0003g0159 |
2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1292-9031G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960125 | |||||||
chr6:75960189 | G | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-9095C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960189 | |||||||
chr6:75960286 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-9192G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960286 | |||||||
chr6:75960314 | C | T | 4 | a0001c0001t0005g0238 a0001c0001t0005g0239 a0002c0002t0001g0155 others(1): Show |
4 | HG02145.hp2 HG02293.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-9220G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960314 | |||||||
chr6:75960365 | A | C | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-9271T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960365 | |||||||
chr6:75960369 | C | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(60): Show |
64 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1292-9275G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960369 | |||||||
chr6:75960400 | A | T | 145 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(142): Show |
146 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1292-9306T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960400 | |||||||
chr6:75960503 | A | C | 3 | a0001c0026t0001g0251 a0003c0015t0001g0012 a0003c0015t0001g0013 |
3 | HG02559.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1292-9409T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960503 | |||||||
chr6:75960613 | C | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(60): Show |
64 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1292-9519G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960613 | |||||||
chr6:75960642 | ATAT | A | 5 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-9551_1292-954 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960642 | |||||||
chr6:75960819 | T | C | 3 | a0001c0001t0001g0257 a0001c0018t0001g0262 a0007c0007t0004g0008 |
3 | HG03540.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-9725A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960819 | |||||||
chr6:75960861 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1292-9767C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75960861 | |||||||
chr6:75961012 | T | A | 78 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0061 others(75): Show |
78 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1292-9918A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961012 | |||||||
chr6:75961449 | A | G | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-10355T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961449 | |||||||
chr6:75961693 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-10599C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961693 | |||||||
chr6:75961856 | C | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1292-10762G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961856 | |||||||
chr6:75961991 | CT | C | 65 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(62): Show |
66 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1292-10898delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75961991 | |||||||
chr6:75962013 | G | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-10919C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962013 | |||||||
chr6:75962102 | C | G | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-11008G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962102 | |||||||
chr6:75962130 | TG | T | 148 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(145): Show |
149 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1292-11037delC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962130 | |||||||
chr6:75962131 | G | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(15): Show |
18 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-11037C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962131 | |||||||
chr6:75962179 | G | T | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1292-11085C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962179 | |||||||
chr6:75962294 | A | T | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-11200T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962294 | |||||||
chr6:75962325 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-11231G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962325 | |||||||
chr6:75962360 | C | T | 2 | a0002c0002t0007g0056 a0002c0002t0007g0255 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1292-11266G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962360 | |||||||
chr6:75962603 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0237 others(3): Show |
6 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-11509G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962603 | |||||||
chr6:75962630 | C | A | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-11536G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962630 | |||||||
chr6:75962633 | C | T | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-11539G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962633 | |||||||
chr6:75962634 | G | A | 65 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(62): Show |
66 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1292-11540C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962634 | |||||||
chr6:75962724 | C | T | 149 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(146): Show |
150 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1292-11630G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962724 | |||||||
chr6:75962753 | T | A | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-11659A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962753 | |||||||
chr6:75962858 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1292-11764A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962858 | |||||||
chr6:75962961 | A | G | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-11867T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962961 | |||||||
chr6:75962997 | C | G | 18 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(15): Show |
18 | HG00621.hp1 HG01993.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-11903G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75962997 | |||||||
chr6:75963032 | C | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(44): Show |
48 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1292-11938G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963032 | |||||||
chr6:75963044 | G | GA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0020 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-11951dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963044 | |||||||
chr6:75963285 | A | G | 1 | a0002c0002t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1292-12191T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963285 | |||||||
chr6:75963379 | C | T | 2 | a0001c0001t0001g0009 a0007c0007t0004g0231 |
2 | HG01261.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1292-12285G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963379 | |||||||
chr6:75963457 | TTTTTA | T | 107 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(104): Show |
108 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1292-12368_1292-12 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963457 | |||||||
chr6:75963744 | G | A | 1 | a0004c0004t0002g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1292-12650C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963744 | |||||||
chr6:75963913 | T | G | 34 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(31): Show |
35 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1292-12819A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963913 | |||||||
chr6:75963946 | A | C | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-12852T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963946 | |||||||
chr6:75963987 | T | G | 1 | a0025c0027t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1292-12893A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75963987 | |||||||
chr6:75964170 | C | A | 3 | a0001c0001t0001g0257 a0001c0018t0001g0262 a0007c0007t0004g0008 |
3 | HG03540.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-13076G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964170 | |||||||
chr6:75964207 | C | T | 1 | a0010c0010t0001g0299 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1292-13113G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964207 | |||||||
chr6:75964227 | A | T | 1 | a0008c0008t0001g0197 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1292-13133T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964227 | |||||||
chr6:75964338 | CAAT | C | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-13247_1292-13 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964338 | |||||||
chr6:75964675 | C | CA | 23 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1292-13582dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | |||||||
chr6:75964675 | C | CAA | 10 | a0001c0001t0001g0004 a0001c0001t0005g0010 a0001c0001t0005g0157 others(7): Show |
10 | HG01169.hp2 HG01993.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-13583_1292-13 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | |||||||
chr6:75964675 | C | CAAA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0051 others(87): Show |
91 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1292-13584_1292-13 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | |||||||
chr6:75964675 | C | CAAAAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0110 others(8): Show |
11 | HG01261.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-13586_1292-13 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | |||||||
chr6:75964675 | CAA | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-13583_1292-13 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75964675 | |||||||
chr6:75965144 | T | C | 1 | a0009c0009t0001g0101 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1292-14050A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965144 | |||||||
chr6:75965365 | CT | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(169): Show |
173 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1292-14272delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965365 | |||||||
chr6:75965523 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1292-14429T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965523 | |||||||
chr6:75965604 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1292-14510A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965604 | |||||||
chr6:75965606 | C | CT | 20 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(17): Show |
20 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-14513dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965606 | |||||||
chr6:75965606 | C | CTT | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1292-14514_1292-14 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965606 | |||||||
chr6:75965606 | C | CTTT | 21 | a0001c0001t0001g0055 a0001c0001t0001g0217 a0001c0001t0001g0256 others(18): Show |
21 | HG01099.hp2 HG01175.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-14515_1292-14 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965606 | |||||||
chr6:75965677 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(200): Show |
205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.1292-14583A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965677 | |||||||
chr6:75965678 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-14584C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965678 | |||||||
chr6:75965678 | G | C | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1292-14584C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965678 | |||||||
chr6:75965682 | T | C | 1 | a0002c0002t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1292-14588A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965682 | |||||||
chr6:75965695 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1292-14601C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965695 | |||||||
chr6:75965707 | A | G | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-14613T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965707 | |||||||
chr6:75965756 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0146 others(1): Show |
4 | HG02896.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-14662A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965756 | |||||||
chr6:75965761 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0146 others(1): Show |
4 | HG02896.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-14667A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965761 | |||||||
chr6:75965780 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1292-14686A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965780 | |||||||
chr6:75965798 | A | G | 1 | a0002c0002t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1292-14704T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965798 | |||||||
chr6:75965828 | C | A | 27 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.1292-14734G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965828 | |||||||
chr6:75965849 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1292-14755A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965849 | |||||||
chr6:75965854 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1292-14760C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965854 | |||||||
chr6:75965875 | A | G | 1 | a0005c0006t0003g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1292-14781T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965875 | |||||||
chr6:75965884 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1292-14790C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965884 | |||||||
chr6:75965887 | A | G | 2 | a0003c0003t0001g0149 a0003c0003t0014g0079 |
2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1292-14793T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965887 | |||||||
chr6:75965889 | G | A | 2 | a0003c0003t0001g0149 a0003c0003t0014g0079 |
2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1292-14795C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75965889 | |||||||
chr6:75966026 | G | A | 1 | a0003c0003t0008g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1292-14932C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966026 | |||||||
chr6:75966094 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-15000C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966094 | |||||||
chr6:75966179 | A | G | 1 | a0017c0028t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1292-15085T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966179 | |||||||
chr6:75966491 | C | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(81): Show |
85 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1292-15397G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966491 | |||||||
chr6:75966591 | T | G | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-15497A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966591 | |||||||
chr6:75966733 | A | C | 54 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(51): Show |
55 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1292-15639T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966733 | |||||||
chr6:75966762 | GAAGA | G | 30 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-15672_1292-15 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966762 | |||||||
chr6:75966767 | A | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1292-15673T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966767 | |||||||
chr6:75966853 | C | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1292-15759G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966853 | |||||||
chr6:75966885 | A | G | 1 | a0002c0002t0001g0126 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-15791T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966885 | |||||||
chr6:75966899 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1292-15805G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966899 | |||||||
chr6:75966946 | G | C | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1292-15852C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966946 | |||||||
chr6:75966998 | C | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(19): Show |
22 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1292-15904G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75966998 | |||||||
chr6:75967089 | G | T | 2 | a0002c0002t0001g0290 a0006c0005t0001g0139 |
2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1292-15995C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967089 | |||||||
chr6:75967176 | A | C | 60 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(57): Show |
60 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1292-16082T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967176 | |||||||
chr6:75967177 | T | TA | 30 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-16084dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967177 | |||||||
chr6:75967253 | C | G | 30 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-16159G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967253 | |||||||
chr6:75967296 | T | C | 3 | a0013c0013t0001g0192 a0013c0013t0001g0193 a0013c0013t0001g0194 |
3 | NA18947.hp1 NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1292-16202A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967296 | |||||||
chr6:75967381 | A | G | 2 | a0002c0002t0001g0147 a0002c0002t0005g0076 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1292-16287T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967381 | |||||||
chr6:75967612 | A | G | 1 | a0006c0005t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1292-16518T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967612 | |||||||
chr6:75967615 | A | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1292-16521T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967615 | |||||||
chr6:75967791 | A | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-16697T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967791 | |||||||
chr6:75967927 | T | A | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-16833A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75967927 | |||||||
chr6:75968122 | A | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-17028T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968122 | |||||||
chr6:75968142 | G | T | 30 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-17048C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968142 | |||||||
chr6:75968274 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1292-17180T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968274 | |||||||
chr6:75968317 | C | T | 30 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-17223G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968317 | |||||||
chr6:75968380 | T | C | 3 | a0001c0001t0001g0257 a0002c0002t0013g0007 a0007c0007t0004g0008 |
3 | HG03453.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1292-17286A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968380 | |||||||
chr6:75968465 | A | AAGTAGAA others(4): Show |
2 | a0002c0002t0013g0007 a0007c0007t0004g0008 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1292-17372_1292-17 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968465 | |||||||
chr6:75968510 | T | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(170): Show |
174 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1292-17416A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968510 | |||||||
chr6:75968581 | C | CT | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-17488dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968581 | |||||||
chr6:75968651 | G | T | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1292-17557C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968651 | |||||||
chr6:75968956 | A | G | 2 | a0001c0001t0001g0274 a0005c0006t0003g0032 |
2 | NA18941.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1292-17862T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75968956 | |||||||
chr6:75969090 | G | C | 59 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(56): Show |
59 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-17996C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969090 | |||||||
chr6:75969261 | G | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(170): Show |
174 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1292-18167C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969261 | |||||||
chr6:75969377 | A | G | 2 | a0001c0001t0001g0274 a0005c0006t0003g0032 |
2 | NA18941.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1292-18283T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969377 | |||||||
chr6:75969630 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0295 |
2 | HG00597.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1292-18536C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969630 | |||||||
chr6:75969731 | A | AAAAC | 19 | a0001c0001t0001g0041 a0002c0002t0001g0129 a0002c0002t0001g0137 others(16): Show |
19 | HG00558.hp2 HG01074.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-18641_1292-18 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969731 | |||||||
chr6:75969731 | AAAAC | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0042 others(19): Show |
22 | HG01070.hp1 HG01516.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.1292-18641_1292-18 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969731 | |||||||
chr6:75969731 | AAAACAAA others(5): Show |
A | 1 | a0002c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1292-18649_1292-18 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969731 | |||||||
chr6:75969939 | T | TA | 3 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 |
3 | HG01070.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1292-18846dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969939 | |||||||
chr6:75969965 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1292-18871A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75969965 | |||||||
chr6:75970082 | T | A | 1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1292-18988A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970082 | |||||||
chr6:75970380 | C | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0237 others(3): Show |
6 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-19286G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970380 | |||||||
chr6:75970491 | T | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-19397A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970491 | |||||||
chr6:75970573 | T | C | 159 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0020 others(156): Show |
160 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1292-19479A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970573 | |||||||
chr6:75970653 | C | T | 3 | a0001c0026t0001g0251 a0002c0002t0001g0078 a0002c0002t0001g0158 |
3 | HG02273.hp2 HG03017.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1292-19559G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970653 | |||||||
chr6:75970654 | G | A | 1 | a0014c0014t0001g0038 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1292-19560C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970654 | |||||||
chr6:75970704 | A | G | 159 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0020 others(156): Show |
160 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1292-19610T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970704 | |||||||
chr6:75970727 | T | C | 7 | a0002c0002t0001g0068 a0002c0002t0001g0093 a0002c0002t0001g0134 others(4): Show |
7 | HG01261.hp2 HG01496.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-19633A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970727 | |||||||
chr6:75970882 | A | G | 1 | a0002c0002t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1292-19788T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75970882 | |||||||
chr6:75971031 | C | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-19937G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971031 | |||||||
chr6:75971066 | C | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-19972G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971066 | |||||||
chr6:75971079 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1292-19985G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971079 | |||||||
chr6:75971146 | T | C | 2 | a0002c0002t0001g0290 a0006c0005t0001g0139 |
2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1292-20052A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971146 | |||||||
chr6:75971211 | C | T | 59 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(56): Show |
59 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-20117G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971211 | |||||||
chr6:75971215 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1292-20121G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971215 | |||||||
chr6:75971239 | G | A | 1 | a0002c0002t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1292-20145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971239 | |||||||
chr6:75971274 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-20180A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971274 | |||||||
chr6:75971276 | C | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-20182G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971276 | |||||||
chr6:75971299 | C | G | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-20205G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971299 | |||||||
chr6:75971331 | G | C | 33 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0004c0004t0001g0233 others(30): Show |
33 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.1292-20237C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971331 | |||||||
chr6:75971369 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-20275C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971369 | |||||||
chr6:75971418 | C | T | 30 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.1292-20324G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971418 | |||||||
chr6:75971474 | TA | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-20381delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971474 | |||||||
chr6:75971477 | A | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(37): Show |
41 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1292-20383T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971477 | |||||||
chr6:75971627 | C | A | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1292-20533G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971627 | |||||||
chr6:75971836 | G | A | 1 | a0007c0007t0004g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1292-20742C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971836 | |||||||
chr6:75971894 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(198): Show |
203 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1292-20800G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971894 | |||||||
chr6:75971912 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1292-20818C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971912 | |||||||
chr6:75971951 | T | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
8 | HG02071.hp2 HG02523.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-20857A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971951 | |||||||
chr6:75971955 | A | T | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-20861T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75971955 | |||||||
chr6:75972175 | C | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(44): Show |
48 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1292-21081G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972175 | |||||||
chr6:75972261 | C | A | 59 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(56): Show |
59 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-21167G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972261 | |||||||
chr6:75972279 | A | G | 3 | a0001c0001t0001g0257 a0002c0002t0013g0007 a0007c0007t0004g0008 |
3 | HG03453.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1292-21185T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972279 | |||||||
chr6:75972404 | C | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-21310G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972404 | |||||||
chr6:75972485 | C | A | 1 | a0003c0003t0014g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1292-21391G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972485 | |||||||
chr6:75972512 | G | A | 3 | a0001c0016t0005g0014 a0001c0016t0005g0015 a0007c0007t0004g0231 |
3 | HG01261.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-21418C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972512 | |||||||
chr6:75972535 | T | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(170): Show |
174 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1292-21441A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972535 | |||||||
chr6:75972538 | G | A | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1292-21444C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972538 | |||||||
chr6:75972608 | T | A | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-21514A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972608 | |||||||
chr6:75972702 | G | A | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-21608C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972702 | |||||||
chr6:75972784 | A | T | 60 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(57): Show |
60 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1292-21690T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972784 | |||||||
chr6:75972829 | T | C | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-21735A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972829 | |||||||
chr6:75972935 | G | T | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-21841C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75972935 | |||||||
chr6:75973123 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1292-22029T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973123 | |||||||
chr6:75973172 | T | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-22078A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973172 | |||||||
chr6:75973242 | A | AGTGTCCG others(47): Show |
2 | a0001c0018t0001g0102 a0003c0003t0001g0075 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1292-22149_1292-22 others(60): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973242 | |||||||
chr6:75973246 | T | TCCGGATT others(20): Show |
44 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0042 others(41): Show |
44 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1292-22179_1292-22 others(33): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973246 | |||||||
chr6:75973246 | T | TCCGGATT others(47): Show |
1 | a0001c0001t0001g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1292-22153_1292-22 others(60): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973246 | |||||||
chr6:75973292 | T | TC | 113 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0023 others(110): Show |
114 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1292-22199dupG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973292 | |||||||
chr6:75973299 | C | CT | 4 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0295 others(1): Show |
4 | HG00597.hp1 NA18987.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-22206_1292-22 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973299 | |||||||
chr6:75973349 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(18): Show |
21 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-22255C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973349 | |||||||
chr6:75973912 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0277 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1292-22818C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973912 | |||||||
chr6:75973918 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(186): Show |
191 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1292-22824A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973918 | |||||||
chr6:75973929 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1292-22835T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75973929 | |||||||
chr6:75974045 | T | C | 1 | a0004c0004t0001g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1292-22951A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974045 | |||||||
chr6:75974115 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0021 others(36): Show |
40 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1292-23021G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974115 | |||||||
chr6:75974245 | ACTTT | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-23155_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974245 | |||||||
chr6:75974258 | CTT | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(19): Show |
22 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-23166_1292-23 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974258 | |||||||
chr6:75974274 | TTCTC | T | 5 | a0003c0003t0006g0005 a0003c0003t0006g0006 a0009c0009t0001g0253 others(2): Show |
5 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-23184_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974274 | |||||||
chr6:75974296 | TTTC | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-23205_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974296 | |||||||
chr6:75974330 | C | CCTTT | 19 | a0002c0002t0001g0048 a0002c0002t0001g0062 a0002c0002t0001g0107 others(16): Show |
19 | HG00558.hp2 HG00609.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1292-23240_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | C | CCTTTCTT others(1): Show |
14 | a0001c0001t0001g0061 a0002c0002t0001g0074 a0002c0002t0001g0120 others(11): Show |
14 | HG01074.hp1 HG01106.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-23244_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | C | CCTTTCTT others(5): Show |
2 | a0006c0005t0002g0089 a0013c0013t0001g0194 |
2 | NA18954.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1292-23248_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | CCTTT | C | 25 | a0002c0002t0001g0059 a0002c0002t0001g0069 a0002c0002t0001g0126 others(22): Show |
25 | HG00735.hp1 HG01070.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1292-23240_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | CCTTTCTT others(1): Show |
C | 19 | a0002c0002t0001g0063 a0002c0002t0001g0245 a0002c0002t0001g0248 others(16): Show |
19 | HG00438.hp2 HG00558.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-23244_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | CCTTTCTT others(5): Show |
C | 13 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0002c0002t0001g0078 others(10): Show |
13 | HG00423.hp1 HG01261.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-23248_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | CCTTTCTT others(9): Show |
C | 3 | a0001c0001t0001g0055 a0002c0002t0001g0121 a0009c0009t0001g0064 |
3 | HG03579.hp1 NA18962.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1292-23252_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974330 | CCTTTCTT others(13): Show |
C | 6 | a0001c0001t0001g0237 a0001c0001t0005g0010 a0001c0001t0009g0260 others(3): Show |
6 | HG02015.hp1 HG02622.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-23256_1292-23 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974330 | |||||||
chr6:75974343 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-23259_1292-23 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974343 | |||||||
chr6:75974356 | TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0001g0282 a0007c0007t0004g0090 |
2 | HG01109.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1292-23281_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974356 | |||||||
chr6:75974359 | C | CTT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1292-23267_1292-23 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974359 | |||||||
chr6:75974360 | TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0277 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1292-23277_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | |||||||
chr6:75974360 | TTTCTTTC others(8): Show |
T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0275 a0001c0001t0001g0280 others(3): Show |
7 | HG00673.hp2 HG02056.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-23281_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | |||||||
chr6:75974360 | TTTCTTTC others(12): Show |
T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0272 a0001c0001t0001g0273 others(6): Show |
9 | HG00140.hp2 HG01074.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-23285_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | |||||||
chr6:75974360 | TTTCTTTC others(16): Show |
T | 1 | a0003c0003t0014g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1292-23289_1292-23 others(29): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974360 | |||||||
chr6:75974364 | TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0001g0286 a0005c0006t0003g0281 |
2 | HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1292-23281_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974364 | |||||||
chr6:75974364 | TTTCTTTC others(8): Show |
T | 2 | a0001c0001t0001g0287 a0005c0006t0003g0291 |
2 | HG01167.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1292-23285_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974364 | |||||||
chr6:75974367 | C | CT | 4 | a0003c0015t0001g0013 a0004c0004t0002g0071 a0014c0014t0001g0038 others(1): Show |
4 | HG02922.hp2 NA18947.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-23274dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974367 | |||||||
chr6:75974368 | TTTC | T | 4 | a0001c0001t0001g0217 a0007c0007t0004g0219 a0007c0007t0004g0228 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-23277_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974368 | |||||||
chr6:75974368 | TTTCTTTC others(12): Show |
T | 2 | a0001c0001t0001g0085 a0003c0003t0001g0083 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1292-23293_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974368 | |||||||
chr6:75974372 | TTTCTTTC others(8): Show |
T | 1 | a0001c0001t0001g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1292-23293_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974372 | |||||||
chr6:75974375 | C | CT | 8 | a0003c0003t0001g0100 a0003c0003t0001g0178 a0005c0006t0003g0080 others(5): Show |
8 | HG00741.hp1 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-23282dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974375 | |||||||
chr6:75974379 | C | CT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0174 others(15): Show |
18 | HG00140.hp1 HG00609.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-23286dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974379 | |||||||
chr6:75974379 | C | CTTTCT | 19 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0070 others(16): Show |
20 | HG01106.hp1 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-23290_1292-23 others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974379 | |||||||
chr6:75974380 | T | C | 2 | a0001c0001t0001g0279 a0003c0015t0001g0012 |
2 | HG02559.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1292-23286A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974380 | |||||||
chr6:75974382 | T | TTCTTTCC others(3): Show |
1 | a0009c0009t0001g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1292-23289_1292-23 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974382 | |||||||
chr6:75974383 | C | CT | 5 | a0001c0001t0001g0188 a0001c0001t0005g0238 a0001c0026t0001g0251 others(2): Show |
5 | HG01099.hp1 HG01169.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-23290dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974383 | |||||||
chr6:75974384 | T | C | 11 | a0001c0001t0001g0265 a0001c0001t0001g0277 a0001c0001t0001g0279 others(8): Show |
11 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-23290A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974384 | |||||||
chr6:75974384 | TTTCTTTC others(5): Show |
T | 1 | a0011c0011t0003g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1292-23302_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974384 | |||||||
chr6:75974386 | T | C | 2 | a0009c0009t0001g0253 a0009c0009t0001g0258 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-23292A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974386 | |||||||
chr6:75974388 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0217 a0001c0001t0001g0265 others(23): Show |
27 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1292-23294A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974388 | |||||||
chr6:75974390 | T | C | 2 | a0009c0009t0001g0253 a0009c0009t0001g0258 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-23296A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974390 | |||||||
chr6:75974391 | C | T | 29 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0026 others(26): Show |
29 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1292-23297G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974391 | |||||||
chr6:75974391 | CT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0034 others(46): Show |
50 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1292-23298delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974391 | |||||||
chr6:75974392 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0026 others(36): Show |
39 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1292-23298A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | |||||||
chr6:75974392 | T | TTTC | 8 | a0001c0001t0001g0188 a0001c0001t0005g0238 a0003c0003t0001g0044 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-23299_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | |||||||
chr6:75974392 | T | TTTCTTTC others(4): Show |
1 | a0003c0003t0001g0152 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1292-23299_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | |||||||
chr6:75974392 | T | TTTCTTTC others(5): Show |
2 | a0003c0003t0001g0030 a0007c0007t0004g0198 |
2 | HG01517.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1292-23299_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | |||||||
chr6:75974392 | T | TTTCTTTT others(1): Show |
5 | a0001c0001t0001g0196 a0001c0001t0001g0224 a0003c0003t0001g0103 others(2): Show |
5 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-23299_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974392 | |||||||
chr6:75974393 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0217 others(31): Show |
35 | HG00140.hp2 HG00673.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1292-23299A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCC | 13 | a0001c0001t0001g0004 a0001c0001t0001g0070 a0001c0001t0001g0173 others(10): Show |
13 | HG01261.hp1 HG02055.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1292-23300_1292-23 others(9): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCCTTCC | 12 | a0001c0001t0001g0182 a0001c0018t0001g0102 a0003c0003t0001g0016 others(9): Show |
13 | HG00609.hp2 HG00741.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-23300_1292-23 others(13): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCCTTCC others(4): Show |
6 | a0001c0001t0001g0041 a0001c0001t0001g0298 a0005c0006t0003g0086 others(3): Show |
6 | HG00140.hp1 HG01106.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-23300_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCCTTCC others(20): Show |
1 | a0005c0006t0003g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(33): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCTTTCC others(4): Show |
1 | a0008c0008t0001g0197 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(17): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCTTTCC others(24): Show |
1 | a0005c0006t0003g0227 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(37): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCTTTCC others(28): Show |
1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(41): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974393 | T | TTCTTTTC others(33): Show |
1 | a0001c0001t0001g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1292-23300_1292-23 others(46): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974393 | |||||||
chr6:75974395 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0274 a0001c0001t0012g0204 others(5): Show |
8 | HG01433.hp2 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-23301A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974395 | |||||||
chr6:75974395 | T | G | 1 | a0003c0015t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1292-23301A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974395 | |||||||
chr6:75974396 | C | T | 1 | a0002c0002t0013g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1292-23302G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974396 | |||||||
chr6:75974397 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(80): Show |
85 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1292-23303A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974397 | |||||||
chr6:75974397 | T | TTCCTTCC others(12): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0274 |
2 | NA18945.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1292-23304_1292-23 others(25): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974397 | |||||||
chr6:75974399 | T | C | 4 | a0001c0001t0012g0204 a0003c0003t0001g0043 a0003c0003t0006g0005 others(1): Show |
4 | HG01433.hp2 HG02965.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-23305A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974399 | |||||||
chr6:75974401 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0020 others(92): Show |
97 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.1292-23307A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTCCTTCC others(8): Show |
4 | a0001c0001t0012g0204 a0003c0003t0001g0043 a0003c0003t0006g0005 others(1): Show |
4 | HG01433.hp2 HG02965.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(21): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCCTTC others(17): Show |
1 | a0005c0006t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCCTTC others(21): Show |
1 | a0001c0001t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(34): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCTTTC others(5): Show |
3 | a0001c0001t0005g0017 a0001c0001t0005g0222 a0004c0004t0002g0024 |
3 | HG02615.hp2 HG02717.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCTTTC others(9): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0271 |
2 | HG02074.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCTTTC others(25): Show |
1 | a0001c0001t0001g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCTTTC others(17): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0295 |
2 | HG00597.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1292-23308_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCTTTC others(25): Show |
1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | T | TTTCTTTC others(29): Show |
1 | a0003c0003t0001g0044 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1292-23308_1292-23 others(42): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974401 | TTTCC | T | 3 | a0004c0004t0002g0114 a0009c0009t0001g0113 a0011c0011t0003g0212 |
3 | HG02129.hp2 NA18957.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1292-23311_1292-23 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974401 | |||||||
chr6:75974404 | C | CCTTCCTT others(13): Show |
1 | a0003c0003t0001g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1292-23311_1292-23 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | |||||||
chr6:75974404 | C | CCTTCCTT others(9): Show |
1 | a0008c0008t0001g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1292-23311_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | |||||||
chr6:75974404 | C | CTTTCCTT others(17): Show |
4 | a0001c0001t0001g0213 a0003c0003t0001g0045 a0010c0010t0001g0199 others(1): Show |
4 | HG00423.hp2 HG02273.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-23311_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | |||||||
chr6:75974404 | C | G | 18 | a0001c0001t0001g0041 a0001c0001t0001g0298 a0004c0004t0002g0027 others(15): Show |
18 | HG00140.hp1 HG00609.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1292-23310G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974404 | |||||||
chr6:75974405 | C | T | 35 | a0001c0001t0001g0053 a0001c0001t0001g0153 a0001c0001t0001g0180 others(32): Show |
35 | HG00423.hp1 HG00558.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1292-23311G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974405 | |||||||
chr6:75974408 | C | CCTTCCTT others(9): Show |
8 | a0001c0001t0001g0196 a0001c0001t0001g0203 a0003c0003t0001g0030 others(5): Show |
8 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-23315_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974408 | |||||||
chr6:75974408 | C | CCTTCCTT others(5): Show |
10 | a0001c0001t0001g0026 a0001c0001t0001g0095 a0001c0001t0001g0185 others(7): Show |
10 | HG00438.hp1 HG00673.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.1292-23315_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974408 | |||||||
chr6:75974408 | C | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0182 others(11): Show |
15 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1292-23314G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974408 | |||||||
chr6:75974409 | C | T | 2 | a0004c0004t0002g0114 a0009c0009t0001g0113 |
2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1292-23315G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974409 | |||||||
chr6:75974412 | C | CCTTCCTT others(5): Show |
9 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0163 others(6): Show |
9 | HG00621.hp1 HG01993.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-23319_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974412 | |||||||
chr6:75974412 | C | CCTTCCTT others(1): Show |
3 | a0001c0001t0001g0023 a0001c0001t0010g0003 a0003c0003t0001g0022 |
3 | HG01928.hp1 HG01952.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1292-23319_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974412 | |||||||
chr6:75974412 | C | G | 13 | a0001c0001t0001g0070 a0001c0001t0001g0173 a0001c0001t0001g0174 others(10): Show |
13 | HG01261.hp1 HG02015.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1292-23318G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974412 | |||||||
chr6:75974416 | C | CCTTCCTT others(1): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0003c0003t0001g0152 |
3 | HG01993.hp2 HG02145.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1292-23323_1292-23 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974416 | |||||||
chr6:75974416 | C | G | 12 | a0001c0001t0001g0034 a0001c0001t0001g0187 a0001c0001t0001g0188 others(9): Show |
12 | HG01099.hp1 HG02293.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1292-23322G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974416 | |||||||
chr6:75974424 | C | G | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-23330G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974424 | |||||||
chr6:75974428 | G | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(151): Show |
156 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1292-23334C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974428 | G | GCTTCCTT others(5): Show |
3 | a0003c0003t0001g0160 a0003c0003t0001g0179 a0003c0003t0001g0210 |
3 | HG01167.hp1 HG01169.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1292-23346_1292-23 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974428 | G | GCTTCCTT others(9): Show |
9 | a0001c0001t0001g0053 a0001c0001t0001g0153 a0001c0001t0001g0180 others(6): Show |
9 | HG01081.hp2 HG01175.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-23350_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974428 | G | GCTTCCTT others(13): Show |
13 | a0004c0004t0001g0233 a0004c0004t0002g0036 a0004c0004t0002g0054 others(10): Show |
13 | HG00423.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-23354_1292-23 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974428 | G | GCTTCCTT others(17): Show |
6 | a0004c0004t0002g0072 a0004c0004t0002g0088 a0004c0004t0002g0097 others(3): Show |
6 | HG00558.hp1 HG02523.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-23358_1292-23 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974428 | G | GCTTCCTT others(25): Show |
1 | a0009c0009t0001g0166 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1292-23335_1292-23 others(38): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974428 | GCTTCCTT others(9): Show |
G | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-23350_1292-23 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974428 | |||||||
chr6:75974451 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1292-23357A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974451 | |||||||
chr6:75974508 | C | T | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1292-23414G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974508 | |||||||
chr6:75974813 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1292-23719C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974813 | |||||||
chr6:75974923 | C | T | 3 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 |
3 | HG02717.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1292-23829G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75974923 | |||||||
chr6:75975383 | G | A | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1292-24289C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975383 | |||||||
chr6:75975433 | C | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0157 a0001c0001t0005g0220 others(2): Show |
5 | HG02615.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-24339G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975433 | |||||||
chr6:75975553 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1292-24459C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975553 | |||||||
chr6:75975594 | C | G | 8 | a0002c0002t0001g0288 a0002c0002t0001g0289 a0004c0004t0002g0128 others(5): Show |
8 | HG00438.hp2 HG00609.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-24500G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975594 | |||||||
chr6:75975595 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(31): Show |
34 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1292-24501A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975595 | |||||||
chr6:75975760 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1292-24666C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975760 | |||||||
chr6:75975998 | C | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(21): Show |
24 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1292-24904G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75975998 | |||||||
chr6:75976153 | A | G | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-25059T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976153 | |||||||
chr6:75976232 | A | G | 1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1292-25138T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976232 | |||||||
chr6:75976293 | G | A | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1292-25199C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976293 | |||||||
chr6:75976417 | C | T | 2 | a0003c0003t0001g0030 a0003c0003t0001g0103 |
2 | HG00738.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1292-25323G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976417 | |||||||
chr6:75976431 | G | A | 1 | a0012c0012t0004g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1292-25337C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976431 | |||||||
chr6:75976439 | G | A | 11 | a0001c0001t0001g0042 a0001c0001t0001g0153 a0001c0001t0001g0180 others(8): Show |
11 | HG01081.hp2 HG01099.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1292-25345C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976439 | |||||||
chr6:75976626 | C | A | 10 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-25532G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976626 | |||||||
chr6:75976696 | G | A | 62 | a0001c0001t0001g0130 a0002c0002t0001g0048 a0002c0002t0001g0065 others(59): Show |
62 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1292-25602C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976696 | |||||||
chr6:75976738 | C | G | 2 | a0001c0018t0001g0262 a0007c0007t0004g0090 |
2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1292-25644G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976738 | |||||||
chr6:75976873 | C | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1292-25779G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976873 | |||||||
chr6:75976884 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(197): Show |
202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1292-25790A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976884 | |||||||
chr6:75976887 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-25793C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976887 | |||||||
chr6:75976909 | TA | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(133): Show |
138 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1292-25816delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75976909 | |||||||
chr6:75977043 | C | T | 5 | a0001c0001t0001g0009 a0007c0007t0004g0241 a0007c0007t0004g0242 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+25875G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977043 | |||||||
chr6:75977044 | G | A | 5 | a0003c0003t0006g0005 a0003c0003t0006g0006 a0009c0009t0001g0253 others(2): Show |
5 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+25874C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977044 | |||||||
chr6:75977094 | A | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1291+25824T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977094 | |||||||
chr6:75977144 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(180): Show |
185 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1291+25774A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977144 | |||||||
chr6:75977154 | T | C | 1 | a0002c0002t0001g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+25764A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977154 | |||||||
chr6:75977385 | C | T | 1 | a0010c0010t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1291+25533G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977385 | |||||||
chr6:75977456 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+25462C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977456 | |||||||
chr6:75977501 | C | T | 10 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(7): Show |
10 | HG01192.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291+25417G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977501 | |||||||
chr6:75977587 | C | CA | 11 | a0001c0001t0001g0095 a0001c0001t0009g0260 a0002c0002t0001g0062 others(8): Show |
11 | HG00673.hp1 HG00738.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291+25330dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977587 | |||||||
chr6:75977587 | CA | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(168): Show |
173 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1291+25330delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977587 | |||||||
chr6:75977590 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+25328T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977590 | |||||||
chr6:75977597 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+25321T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977597 | |||||||
chr6:75977602 | C | A | 1 | a0006c0005t0002g0096 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1291+25316G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977602 | |||||||
chr6:75977611 | A | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1291+25307T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977611 | |||||||
chr6:75977665 | A | C | 1 | a0001c0001t0005g0018 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1291+25253T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977665 | |||||||
chr6:75977716 | G | A | 20 | a0002c0002t0001g0062 a0002c0002t0001g0063 a0002c0002t0001g0141 others(17): Show |
20 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1291+25202C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977716 | |||||||
chr6:75977822 | C | T | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1291+25096G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75977822 | |||||||
chr6:75978037 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291+24881C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978037 | |||||||
chr6:75978129 | T | TTATATAC others(3): Show |
2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+24779_1291+24 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978129 | |||||||
chr6:75978253 | T | C | 1 | a0011c0011t0003g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1291+24665A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978253 | |||||||
chr6:75978323 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(185): Show |
190 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1291+24595G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978323 | |||||||
chr6:75978463 | A | G | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+24455T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978463 | |||||||
chr6:75978474 | TG | T | 10 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+24443delC | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978474 | |||||||
chr6:75978803 | T | C | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+24115A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75978803 | |||||||
chr6:75979006 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1291+23912C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979006 | |||||||
chr6:75979089 | C | T | 1 | a0002c0002t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1291+23829G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979089 | |||||||
chr6:75979153 | G | A | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1291+23765C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979153 | |||||||
chr6:75979197 | G | A | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+23721C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979197 | |||||||
chr6:75979211 | C | T | 1 | a0017c0028t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1291+23707G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979211 | |||||||
chr6:75979583 | C | T | 1 | a0002c0002t0001g0126 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1291+23335G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979583 | |||||||
chr6:75979597 | A | T | 1 | a0014c0014t0001g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1291+23321T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979597 | |||||||
chr6:75979631 | C | A | 1 | a0002c0002t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291+23287G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979631 | |||||||
chr6:75979716 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1291+23202C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979716 | |||||||
chr6:75979736 | G | C | 1 | a0025c0027t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1291+23182C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979736 | |||||||
chr6:75979817 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1291+23101T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979817 | |||||||
chr6:75979892 | A | G | 6 | a0004c0004t0002g0071 a0014c0014t0001g0038 a0014c0014t0001g0040 others(3): Show |
6 | NA18947.hp2 NA18969.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+23026T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979892 | |||||||
chr6:75979922 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291+22996A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75979922 | |||||||
chr6:75980135 | A | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+22783T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980135 | |||||||
chr6:75980322 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(184): Show |
189 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1291+22596G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980322 | |||||||
chr6:75980344 | A | G | 6 | a0001c0026t0001g0251 a0003c0003t0006g0005 a0003c0003t0006g0006 others(3): Show |
6 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+22574T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980344 | |||||||
chr6:75980414 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(184): Show |
189 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1291+22504G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980414 | |||||||
chr6:75980583 | G | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1291+22335C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980583 | |||||||
chr6:75980596 | A | G | 1 | a0002c0002t0001g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+22322T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980596 | |||||||
chr6:75980710 | C | A | 1 | a0010c0010t0001g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1291+22208G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980710 | |||||||
chr6:75980884 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+22034C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75980884 | |||||||
chr6:75981107 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1291+21811T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981107 | |||||||
chr6:75981148 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(9): Show |
12 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+21770G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981148 | |||||||
chr6:75981195 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+21723C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981195 | |||||||
chr6:75981238 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+21680G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981238 | |||||||
chr6:75981626 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1291+21292G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981626 | |||||||
chr6:75981819 | G | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+21099C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981819 | |||||||
chr6:75981836 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1291+21082A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75981836 | |||||||
chr6:75982059 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(131): Show |
136 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1291+20859G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982059 | |||||||
chr6:75982196 | C | A | 2 | a0003c0003t0006g0005 a0003c0003t0006g0006 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+20722G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982196 | |||||||
chr6:75982293 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00140.hp2 HG00673.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1291+20625A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982293 | |||||||
chr6:75982321 | T | A | 1 | a0009c0009t0001g0101 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1291+20597A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982321 | |||||||
chr6:75982397 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1291+20521G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982397 | |||||||
chr6:75982464 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1291+20454G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982464 | |||||||
chr6:75982511 | G | A | 66 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0173 others(63): Show |
66 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1291+20407C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982511 | |||||||
chr6:75982536 | T | A | 1 | a0004c0004t0002g0175 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1291+20382A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982536 | |||||||
chr6:75982541 | A | ATATC | 5 | a0001c0001t0001g0009 a0009c0009t0001g0253 a0009c0009t0001g0258 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+20373_1291+20 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982541 | A | ATATCTAT others(1): Show |
129 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(126): Show |
131 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1291+20369_1291+20 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982541 | A | ATATCTAT others(5): Show |
13 | a0001c0001t0001g0053 a0001c0001t0001g0280 a0001c0001t0001g0298 others(10): Show |
13 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291+20365_1291+20 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982541 | A | ATATCTAT others(9): Show |
1 | a0002c0002t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1291+20361_1291+20 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982541 | A | ATATCTAT others(13): Show |
3 | a0001c0001t0005g0220 a0002c0002t0001g0226 a0012c0012t0004g0229 |
3 | HG02559.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1291+20357_1291+20 others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982541 | A | ATATCTAT others(17): Show |
1 | a0004c0004t0002g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1291+20376_1291+20 others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982541 | ATATC | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 |
3 | HG02257.hp2 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1291+20373_1291+20 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982541 | |||||||
chr6:75982586 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1291+20332C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982586 | |||||||
chr6:75982586 | GATATATA others(11): Show |
G | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+20314_1291+20 others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982586 | |||||||
chr6:75982586 | GATATATA others(29): Show |
G | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+20296_1291+20 others(42): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982586 | |||||||
chr6:75982698 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+20220T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982698 | |||||||
chr6:75982829 | G | C | 2 | a0003c0003t0006g0005 a0003c0003t0006g0006 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+20089C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75982829 | |||||||
chr6:75983048 | T | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(186): Show |
191 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1291+19870A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983048 | |||||||
chr6:75983772 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+19146C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983772 | |||||||
chr6:75983826 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+19092C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983826 | |||||||
chr6:75983870 | GC | G | 12 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(9): Show |
12 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+19047delG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75983870 | |||||||
chr6:75984229 | G | C | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1291+18689C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984229 | |||||||
chr6:75984785 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+18133A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984785 | |||||||
chr6:75984922 | T | G | 11 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(8): Show |
11 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1291+17996A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984922 | |||||||
chr6:75984938 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+17980C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984938 | |||||||
chr6:75984956 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+17962G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984956 | |||||||
chr6:75984957 | C | A | 1 | a0002c0002t0001g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1291+17961G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75984957 | |||||||
chr6:75985038 | A | G | 2 | a0002c0002t0001g0288 a0002c0002t0001g0289 |
2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1291+17880T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985038 | |||||||
chr6:75985109 | A | G | 9 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291+17809T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985109 | |||||||
chr6:75985284 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1291+17634C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985284 | |||||||
chr6:75985332 | C | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+17586G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985332 | |||||||
chr6:75985481 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(190): Show |
195 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.1291+17437T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985481 | |||||||
chr6:75985548 | GA | G | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+17369delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985548 | |||||||
chr6:75985583 | C | T | 1 | a0003c0003t0001g0210 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1291+17335G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985583 | |||||||
chr6:75985599 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1291+17319G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985599 | |||||||
chr6:75985606 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+17312A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985606 | |||||||
chr6:75985697 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1291+17221C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985697 | |||||||
chr6:75985928 | T | C | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1291+16990A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985928 | |||||||
chr6:75985984 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1291+16934T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75985984 | |||||||
chr6:75986004 | A | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+16914T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986004 | |||||||
chr6:75986080 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(148): Show |
153 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1291+16838A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986080 | |||||||
chr6:75986186 | G | A | 1 | a0019c0019t0003g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1291+16732C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986186 | |||||||
chr6:75986251 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+16667G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986251 | |||||||
chr6:75986482 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+16436G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986482 | |||||||
chr6:75986519 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1291+16399A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986519 | |||||||
chr6:75986745 | GA | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+16172delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986745 | |||||||
chr6:75986810 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1291+16108C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986810 | |||||||
chr6:75986826 | CA | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 |
3 | HG02257.hp2 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1291+16091delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75986826 | |||||||
chr6:75987037 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1291+15881C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987037 | |||||||
chr6:75987048 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+15870G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987048 | |||||||
chr6:75987301 | C | CT | 116 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(113): Show |
117 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1291+15616dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987301 | |||||||
chr6:75987301 | CT | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(26): Show |
30 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1291+15616delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987301 | |||||||
chr6:75987343 | T | C | 16 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0052 others(13): Show |
16 | HG00621.hp1 HG01175.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291+15575A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987343 | |||||||
chr6:75987354 | C | T | 1 | a0005c0006t0003g0227 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1291+15564G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987354 | |||||||
chr6:75987373 | T | C | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+15545A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987373 | |||||||
chr6:75987453 | C | CG | 4 | a0001c0001t0001g0110 a0002c0002t0001g0294 a0015c0017t0001g0292 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+15464_1291+15 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987453 | |||||||
chr6:75987454 | T | C | 5 | a0001c0001t0001g0110 a0002c0002t0001g0294 a0013c0013t0001g0181 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+15464A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987454 | |||||||
chr6:75987454 | T | G | 6 | a0001c0001t0001g0225 a0001c0001t0001g0256 a0001c0001t0005g0157 others(3): Show |
6 | HG02257.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+15464A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987454 | |||||||
chr6:75987454 | T | TC | 40 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0061 others(37): Show |
40 | HG00621.hp1 HG00738.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1291+15463dupG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987454 | |||||||
chr6:75987471 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1291+15447G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987471 | |||||||
chr6:75987600 | T | C | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1291+15318A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987600 | |||||||
chr6:75987647 | C | CT | 148 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(145): Show |
150 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1291+15270dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987647 | |||||||
chr6:75987685 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+15233G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987685 | |||||||
chr6:75987745 | C | T | 8 | a0002c0002t0001g0288 a0002c0002t0001g0289 a0004c0004t0002g0128 others(5): Show |
8 | HG00438.hp2 HG00609.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291+15173G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987745 | |||||||
chr6:75987805 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+15113G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987805 | |||||||
chr6:75987866 | T | C | 5 | a0007c0007t0004g0231 a0007c0007t0004g0241 a0007c0007t0004g0242 others(2): Show |
5 | HG01261.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+15052A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987866 | |||||||
chr6:75987898 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+15020G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987898 | |||||||
chr6:75987972 | T | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(149): Show |
154 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1291+14946A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987972 | |||||||
chr6:75987991 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1291+14927G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75987991 | |||||||
chr6:75988017 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+14901T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988017 | |||||||
chr6:75988021 | T | C | 9 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291+14897A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988021 | |||||||
chr6:75988242 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+14676A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988242 | |||||||
chr6:75988307 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+14611G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988307 | |||||||
chr6:75988345 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(201): Show |
206 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1291+14573G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988345 | |||||||
chr6:75988442 | A | G | 63 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0091 others(60): Show |
64 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1291+14476T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988442 | |||||||
chr6:75988450 | C | G | 2 | a0003c0003t0006g0005 a0003c0003t0006g0006 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+14468G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988450 | |||||||
chr6:75988485 | T | G | 1 | a0017c0028t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1291+14433A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988485 | |||||||
chr6:75988751 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(149): Show |
154 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1291+14167A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988751 | |||||||
chr6:75988757 | T | C | 1 | a0006c0005t0008g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1291+14161A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988757 | |||||||
chr6:75988775 | A | C | 1 | a0005c0006t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1291+14143T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988775 | |||||||
chr6:75988955 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+13963T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75988955 | |||||||
chr6:75989049 | C | CA | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+13868_1291+13 others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989049 | |||||||
chr6:75989366 | A | G | 1 | a0001c0001t0005g0238 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1291+13552T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989366 | |||||||
chr6:75989425 | T | C | 13 | a0002c0002t0001g0048 a0002c0002t0001g0069 a0002c0002t0001g0136 others(10): Show |
13 | HG02135.hp2 HG02602.hp2 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.1291+13493A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989425 | |||||||
chr6:75989443 | T | C | 2 | a0002c0002t0001g0150 a0003c0003t0001g0149 |
2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1291+13475A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989443 | |||||||
chr6:75989550 | A | G | 1 | a0011c0011t0003g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1291+13368T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989550 | |||||||
chr6:75989564 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0057 others(2): Show |
5 | HG02896.hp1 HG03209.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+13354G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989564 | |||||||
chr6:75989599 | T | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+13319A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989599 | |||||||
chr6:75989900 | A | C | 1 | a0008c0008t0001g0197 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1291+13018T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75989900 | |||||||
chr6:75990182 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+12736C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990182 | |||||||
chr6:75990259 | A | C | 4 | a0001c0001t0001g0091 a0004c0004t0002g0054 a0004c0004t0002g0094 others(1): Show |
4 | HG00423.hp1 HG00558.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+12659T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990259 | |||||||
chr6:75990579 | C | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(151): Show |
156 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1291+12339G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990579 | |||||||
chr6:75990588 | T | TAC | 46 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(43): Show |
47 | HG00673.hp2 HG00741.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1291+12328_1291+12 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | |||||||
chr6:75990588 | T | TACAC | 16 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0001g0263 others(13): Show |
17 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+12326_1291+12 others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | |||||||
chr6:75990588 | T | TACACAC | 33 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+12324_1291+12 others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | |||||||
chr6:75990588 | T | TACACACA others(1): Show |
83 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(80): Show |
83 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1291+12322_1291+12 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | |||||||
chr6:75990588 | T | TACACACA others(3): Show |
17 | a0001c0001t0001g0180 a0001c0001t0001g0187 a0001c0001t0001g0188 others(14): Show |
17 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+12320_1291+12 others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | |||||||
chr6:75990588 | T | TACACACA others(5): Show |
12 | a0001c0001t0001g0196 a0003c0003t0001g0029 a0003c0003t0001g0030 others(9): Show |
12 | HG00140.hp1 HG00597.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1291+12318_1291+12 others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990588 | |||||||
chr6:75990773 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+12145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990773 | |||||||
chr6:75990793 | CA | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+12124delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990793 | |||||||
chr6:75990873 | T | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+12045A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75990873 | |||||||
chr6:75991007 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0003c0003t0001g0083 |
3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1291+11911T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991007 | |||||||
chr6:75991059 | T | G | 1 | a0002c0002t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1291+11859A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991059 | |||||||
chr6:75991106 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+11812A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991106 | |||||||
chr6:75991233 | T | C | 3 | a0001c0001t0005g0010 a0001c0001t0005g0220 a0001c0001t0005g0223 |
3 | HG03453.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1291+11685A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991233 | |||||||
chr6:75991315 | C | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+11603G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991315 | |||||||
chr6:75991349 | C | G | 1 | a0001c0001t0001g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1291+11569G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991349 | |||||||
chr6:75991382 | C | G | 10 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1291+11536G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991382 | |||||||
chr6:75991396 | T | TA | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0110 others(10): Show |
13 | HG01884.hp2 HG02027.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1291+11521dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991396 | |||||||
chr6:75991396 | TAA | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+11520_1291+11 others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991396 | |||||||
chr6:75991567 | A | G | 2 | a0002c0002t0007g0056 a0002c0002t0007g0255 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1291+11351T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991567 | |||||||
chr6:75991649 | G | A | 1 | a0007c0007t0004g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+11269C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991649 | |||||||
chr6:75991743 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+11175A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75991743 | |||||||
chr6:75992072 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+10846C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992072 | |||||||
chr6:75992164 | C | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+10754G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992164 | |||||||
chr6:75992450 | C | T | 3 | a0004c0004t0002g0071 a0022c0021t0002g0098 a0023c0020t0001g0039 |
3 | NA18947.hp2 NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1291+10468G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992450 | |||||||
chr6:75992581 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1291+10337G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992581 | |||||||
chr6:75992711 | C | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+10207G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992711 | |||||||
chr6:75992758 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1291+10160G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992758 | |||||||
chr6:75992801 | T | G | 117 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(114): Show |
118 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1291+10117A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992801 | |||||||
chr6:75992834 | G | A | 1 | a0007c0007t0004g0008 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1291+10084C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992834 | |||||||
chr6:75992993 | C | T | 1 | a0001c0001t0012g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1291+9925G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75992993 | |||||||
chr6:75993298 | C | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(24): Show |
28 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+9620G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993298 | |||||||
chr6:75993479 | AGAGAGAA others(3): Show |
A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+9429_1291+943 others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993479 | |||||||
chr6:75993499 | GGAGAGAG others(11): Show |
G | 1 | a0004c0004t0002g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1291+9401_1291+941 others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993499 | |||||||
chr6:75993660 | T | A | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+9258A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993660 | |||||||
chr6:75993715 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+9203T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993715 | |||||||
chr6:75993797 | T | TAAAAGTT others(1586): Show |
1 | a0010c0010t0001g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1291+9120_1291+912 others(1597): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993797 | |||||||
chr6:75993847 | T | C | 1 | a0018c0029t0001g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1291+9071A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993847 | |||||||
chr6:75993864 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+9054T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993864 | |||||||
chr6:75993948 | T | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+8970A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993948 | |||||||
chr6:75993993 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1291+8925A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75993993 | |||||||
chr6:75994179 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+8739C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994179 | |||||||
chr6:75994334 | T | C | 1 | a0006c0005t0002g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1291+8584A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994334 | |||||||
chr6:75994411 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1291+8507G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994411 | |||||||
chr6:75994597 | G | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+8321C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994597 | |||||||
chr6:75994772 | G | A | 2 | a0002c0002t0007g0056 a0002c0002t0007g0255 |
2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1291+8146C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994772 | |||||||
chr6:75994956 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+7962C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75994956 | |||||||
chr6:75995037 | C | T | 1 | a0007c0007t0004g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+7881G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995037 | |||||||
chr6:75995363 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1291+7555C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995363 | |||||||
chr6:75995374 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0035 others(2): Show |
5 | HG00597.hp1 HG02074.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+7544G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995374 | |||||||
chr6:75995385 | T | C | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+7533A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995385 | |||||||
chr6:75995486 | C | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(24): Show |
28 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+7432G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995486 | |||||||
chr6:75995594 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(42): Show |
45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+7324G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75995594 | |||||||
chr6:75996045 | T | C | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+6873A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996045 | |||||||
chr6:75996159 | G | T | 109 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(106): Show |
110 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1291+6759C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996159 | |||||||
chr6:75996160 | C | T | 21 | a0001c0001t0001g0061 a0002c0002t0001g0062 a0002c0002t0001g0063 others(18): Show |
21 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.1291+6758G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996160 | |||||||
chr6:75996316 | C | A | 1 | a0005c0006t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1291+6602G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996316 | |||||||
chr6:75996567 | G | C | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+6351C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996567 | |||||||
chr6:75996722 | ATGTAATA others(12): Show |
A | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291+6177_1291+619 others(23): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75996722 | |||||||
chr6:75997060 | A | C | 1 | a0002c0002t0001g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1291+5858T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997060 | |||||||
chr6:75997101 | T | C | 3 | a0004c0004t0002g0114 a0005c0006t0003g0032 a0009c0009t0001g0113 |
3 | HG02129.hp2 NA18941.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1291+5817A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997101 | |||||||
chr6:75997136 | G | A | 1 | a0008c0008t0001g0135 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1291+5782C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997136 | |||||||
chr6:75997318 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1291+5600G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997318 | |||||||
chr6:75997353 | T | C | 11 | a0001c0001t0001g0095 a0002c0002t0001g0068 a0002c0002t0001g0134 others(8): Show |
11 | HG00673.hp1 HG00735.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+5565A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997353 | |||||||
chr6:75997702 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1291+5216C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997702 | |||||||
chr6:75997714 | A | T | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+5204T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997714 | |||||||
chr6:75997723 | T | C | 1 | a0021c0023t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1291+5195A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997723 | |||||||
chr6:75997865 | T | A | 4 | a0001c0001t0001g0061 a0002c0002t0001g0062 a0002c0002t0001g0063 others(1): Show |
4 | HG03139.hp2 HG03209.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+5053A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997865 | |||||||
chr6:75997941 | G | A | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+4977C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75997941 | |||||||
chr6:75998102 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1291+4816G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998102 | |||||||
chr6:75998200 | A | G | 8 | a0002c0002t0001g0288 a0002c0002t0001g0289 a0004c0004t0002g0128 others(5): Show |
8 | HG00438.hp2 HG00609.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291+4718T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998200 | |||||||
chr6:75998450 | G | A | 1 | a0009c0009t0001g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1291+4468C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998450 | |||||||
chr6:75998514 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+4404C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998514 | |||||||
chr6:75998672 | T | G | 1 | a0014c0014t0001g0040 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1291+4246A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998672 | |||||||
chr6:75998717 | C | T | 1 | a0006c0005t0008g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1291+4201G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998717 | |||||||
chr6:75998743 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(24): Show |
28 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+4175G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998743 | |||||||
chr6:75998950 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+3968T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75998950 | |||||||
chr6:75999077 | G | A | 9 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0256 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291+3841C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999077 | |||||||
chr6:75999089 | TC | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+3828delG | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999089 | |||||||
chr6:75999165 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1291+3753A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999165 | |||||||
chr6:75999237 | T | C | 1 | a0003c0003t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1291+3681A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999237 | |||||||
chr6:75999261 | A | ACATACCA others(300): Show |
4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+3656_1291+365 others(311): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999261 | |||||||
chr6:75999275 | T | C | 1 | a0013c0013t0001g0192 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1291+3643A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999275 | |||||||
chr6:75999501 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(42): Show |
45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+3417C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999501 | |||||||
chr6:75999506 | G | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+3412C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999506 | |||||||
chr6:75999551 | C | T | 1 | a0008c0008t0001g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1291+3367G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999551 | |||||||
chr6:75999555 | G | A | 1 | a0004c0004t0002g0235 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1291+3363C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999555 | |||||||
chr6:75999607 | G | A | 1 | a0002c0002t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1291+3311C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999607 | |||||||
chr6:75999807 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(202): Show |
207 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1291+3111G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999807 | |||||||
chr6:75999857 | A | G | 1 | a0002c0002t0001g0126 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1291+3061T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999857 | |||||||
chr6:75999919 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+2999G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999919 | |||||||
chr6:75999931 | T | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(42): Show |
45 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1291+2987A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 75999931 | |||||||
chr6:76000081 | C | T | 1 | a0003c0003t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1291+2837G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000081 | |||||||
chr6:76000438 | A | G | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1291+2480T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000438 | |||||||
chr6:76000624 | C | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0265 others(20): Show |
24 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1291+2294G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000624 | |||||||
chr6:76000755 | A | C | 1 | a0002c0002t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1291+2163T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000755 | |||||||
chr6:76000759 | C | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+2159G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000759 | |||||||
chr6:76000760 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1291+2158G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000760 | |||||||
chr6:76000830 | G | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+2088C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000830 | |||||||
chr6:76000958 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+1960T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76000958 | |||||||
chr6:76001074 | C | A | 2 | a0002c0002t0001g0252 a0002c0002t0001g0261 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1291+1844G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001074 | |||||||
chr6:76001145 | T | C | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1291+1773A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001145 | |||||||
chr6:76001253 | T | C | 2 | a0002c0002t0013g0007 a0007c0007t0004g0008 |
2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1291+1665A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001253 | |||||||
chr6:76001332 | C | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1291+1586G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001332 | |||||||
chr6:76001812 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1291+1106A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001812 | |||||||
chr6:76001894 | A | G | 1 | a0007c0007t0004g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1291+1024T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76001894 | |||||||
chr6:76002054 | G | A | 272 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(269): Show |
274 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.1291+864C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002054 | |||||||
chr6:76002092 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0005g0017 a0001c0001t0005g0018 others(5): Show |
8 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+826T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002092 | |||||||
chr6:76002372 | G | C | 1 | a0006c0005t0011g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1291+546C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002372 | |||||||
chr6:76002648 | C | T | 26 | a0001c0001t0001g0042 a0002c0002t0001g0093 a0003c0003t0001g0100 others(23): Show |
26 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.1291+270G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002648 | |||||||
chr6:76002718 | C | T | 6 | a0003c0003t0006g0005 a0003c0003t0006g0006 a0007c0007t0004g0241 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+200G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002718 | |||||||
chr6:76002735 | T | C | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1291+183A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002735 | |||||||
chr6:76002751 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1291+167G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002751 | |||||||
chr6:76002813 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291+105G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 12/16 | chr6 | 76002813 | |||||||
chr6:76003248 | C | T | 1 | a0017c0028t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1213-252G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003248 | |||||||
chr6:76003453 | C | T | 1 | a0002c0002t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1212+421G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003453 | |||||||
chr6:76003545 | T | C | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1212+329A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003545 | |||||||
chr6:76003816 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1212+58A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 11/16 | chr6 | 76003816 | |||||||
chr6:76004037 | C | T | 113 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(110): Show |
114 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1136-87G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004037 | |||||||
chr6:76004038 | G | A | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1136-88C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004038 | |||||||
chr6:76004065 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1136-115G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004065 | |||||||
chr6:76004138 | A | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(13): Show |
16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136-188T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004138 | |||||||
chr6:76004185 | G | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1136-235C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004185 | |||||||
chr6:76004297 | A | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(23): Show |
26 | HG02145.hp1 HG02280.hp1 HG02293.hp2 others(23): Show |
intron_variant | MODIFIER | c.1136-347T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004297 | |||||||
chr6:76004462 | C | T | 1 | a0003c0003t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1136-512G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004462 | |||||||
chr6:76004463 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136-513C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004463 | |||||||
chr6:76004532 | C | T | 1 | a0010c0010t0001g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1136-582G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004532 | |||||||
chr6:76004647 | C | A | 113 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(110): Show |
114 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1135+640G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004647 | |||||||
chr6:76004852 | T | C | 4 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135+435A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004852 | |||||||
chr6:76004880 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135+407G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004880 | |||||||
chr6:76004997 | C | G | 2 | a0002c0002t0001g0184 a0003c0003t0001g0172 |
2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1135+290G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76004997 | |||||||
chr6:76005016 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(142): Show |
146 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1135+271A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005016 | |||||||
chr6:76005024 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1135+263G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005024 | |||||||
chr6:76005079 | T | C | 5 | a0001c0001t0001g0011 a0002c0002t0007g0056 a0002c0002t0013g0007 others(2): Show |
5 | HG01109.hp1 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135+208A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005079 | |||||||
chr6:76005209 | C | T | 1 | a0001c0001t0005g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1135+78G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005209 | |||||||
chr6:76005222 | A | G | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1135+65T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 10/16 | chr6 | 76005222 | |||||||
chr6:76005582 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.888-48C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76005582 | |||||||
chr6:76005825 | T | A | 3 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 |
3 | HG01070.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.888-291A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76005825 | |||||||
chr6:76005827 | TTTTC | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(20): Show |
23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.888-297_888-294del others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76005827 | |||||||
chr6:76006133 | C | G | 3 | a0020c0024t0001g0132 a0021c0023t0001g0127 a0024c0022t0001g0050 |
3 | NA18946.hp2 NA18948.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.888-599G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006133 | |||||||
chr6:76006183 | T | C | 4 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(1): Show |
4 | HG02647.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.888-649A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006183 | |||||||
chr6:76006209 | G | A | 100 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0130 others(97): Show |
100 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.888-675C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006209 | |||||||
chr6:76006348 | A | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.888-814T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006348 | |||||||
chr6:76006455 | TGTGTATA others(15): Show |
T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0061 others(125): Show |
129 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.888-943_888-922del others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006455 | |||||||
chr6:76006519 | G | T | 1 | a0001c0001t0005g0223 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.887+961C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006519 | |||||||
chr6:76006520 | G | A | 1 | a0001c0001t0005g0223 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.887+960C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006520 | |||||||
chr6:76006529 | C | CGT | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.887+949_887+950dup others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006529 | |||||||
chr6:76006550 | A | G | 3 | a0002c0002t0013g0007 a0007c0007t0004g0008 a0007c0007t0004g0090 |
3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.887+930T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006550 | |||||||
chr6:76006551 | T | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.887+929A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006551 | |||||||
chr6:76006568 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.887+912C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006568 | |||||||
chr6:76006683 | C | T | 100 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0130 others(97): Show |
100 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.887+797G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006683 | |||||||
chr6:76006907 | A | G | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.887+573T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76006907 | |||||||
chr6:76007025 | C | T | 118 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0034 others(115): Show |
119 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.887+455G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007025 | |||||||
chr6:76007163 | G | A | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.887+317C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007163 | |||||||
chr6:76007184 | C | T | 99 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0130 others(96): Show |
99 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.887+296G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007184 | |||||||
chr6:76007275 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02027.hp2 HG02071.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+205T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007275 | |||||||
chr6:76007300 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.887+180C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007300 | |||||||
chr6:76007302 | A | AT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.887+177dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007302 | |||||||
chr6:76007302 | AT | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(27): Show |
31 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.887+177delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007302 | |||||||
chr6:76007440 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(26): Show |
30 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.887+40G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 9/16 | chr6 | 76007440 | |||||||
chr6:76007552 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867-52C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007552 | |||||||
chr6:76007691 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.867-191C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007691 | |||||||
chr6:76007818 | G | A | 1 | a0004c0004t0002g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.867-318C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007818 | |||||||
chr6:76007832 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.867-332G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007832 | |||||||
chr6:76007832 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.867-332G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76007832 | |||||||
chr6:76008046 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0061 others(125): Show |
129 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.867-546C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008046 | |||||||
chr6:76008290 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.867-790G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008290 | |||||||
chr6:76008566 | G | A | 2 | a0002c0002t0001g0296 a0002c0002t0001g0297 |
2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.867-1066C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008566 | |||||||
chr6:76008797 | C | T | 111 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(108): Show |
112 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.867-1297G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008797 | |||||||
chr6:76008861 | C | T | 1 | a0010c0010t0001g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.867-1361G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76008861 | |||||||
chr6:76009088 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.867-1588A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009088 | |||||||
chr6:76009294 | G | C | 1 | a0002c0002t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.867-1794C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009294 | |||||||
chr6:76009542 | G | A | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.866+1624C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009542 | |||||||
chr6:76009702 | T | TA | 3 | a0002c0002t0001g0230 a0003c0003t0001g0075 a0012c0012t0004g0229 |
3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.866+1463dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009702 | |||||||
chr6:76009978 | T | G | 23 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0180 others(20): Show |
23 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.866+1188A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76009978 | |||||||
chr6:76010054 | A | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0203 others(27): Show |
31 | HG00140.hp1 HG00438.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.866+1112T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010054 | |||||||
chr6:76010294 | G | A | 1 | a0001c0018t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.866+872C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010294 | |||||||
chr6:76010382 | T | C | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.866+784A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010382 | |||||||
chr6:76010384 | T | C | 3 | a0002c0002t0001g0230 a0003c0003t0001g0075 a0012c0012t0004g0229 |
3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.866+782A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010384 | |||||||
chr6:76010487 | C | T | 21 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01358.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.866+679G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010487 | |||||||
chr6:76010548 | C | G | 1 | a0001c0001t0001g0275 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.866+618G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010548 | |||||||
chr6:76010577 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.866+589C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010577 | |||||||
chr6:76010633 | G | A | 1 | a0010c0010t0001g0278 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.866+533C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010633 | |||||||
chr6:76010779 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.866+387G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010779 | |||||||
chr6:76010835 | C | T | 273 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(270): Show |
275 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.866+331G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010835 | |||||||
chr6:76010867 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.866+299G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010867 | |||||||
chr6:76010888 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.866+278G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76010888 | |||||||
chr6:76011034 | C | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(142): Show |
146 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.866+132G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76011034 | |||||||
chr6:76011057 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0005g0010 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.866+109C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 8/16 | chr6 | 76011057 | |||||||
chr6:76011242 | TTTGTAAA others(6): Show |
T | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.808-31_808-19delGA others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011242 | |||||||
chr6:76011273 | A | T | 112 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(109): Show |
113 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.808-49T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011273 | |||||||
chr6:76011394 | T | C | 4 | a0001c0001t0001g0236 a0003c0003t0001g0232 a0003c0003t0001g0234 others(1): Show |
4 | NA18970.hp1 NA18987.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.808-170A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011394 | |||||||
chr6:76011508 | G | A | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.808-284C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011508 | |||||||
chr6:76011736 | T | C | 1 | a0011c0011t0003g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.808-512A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011736 | |||||||
chr6:76011737 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.808-513G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011737 | |||||||
chr6:76011910 | T | A | 1 | a0002c0002t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.808-686A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011910 | |||||||
chr6:76011981 | A | G | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.808-757T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76011981 | |||||||
chr6:76012003 | C | G | 3 | a0006c0005t0001g0170 a0011c0011t0003g0124 a0011c0011t0003g0125 |
3 | HG01256.hp1 HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.808-779G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012003 | |||||||
chr6:76012040 | TTATC | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(20): Show |
23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.808-820_808-817del others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012040 | |||||||
chr6:76012068 | A | G | 1 | a0002c0002t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.808-844T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012068 | |||||||
chr6:76012084 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0005g0010 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.808-860C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012084 | |||||||
chr6:76012128 | T | G | 2 | a0004c0004t0002g0240 a0009c0009t0001g0111 |
2 | NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.808-904A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012128 | |||||||
chr6:76012550 | C | A | 1 | a0006c0005t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.808-1326G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012550 | |||||||
chr6:76012600 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0230 others(3): Show |
6 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-1376C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012600 | |||||||
chr6:76012634 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(20): Show |
23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.808-1410C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012634 | |||||||
chr6:76012758 | C | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(20): Show |
23 | HG02145.hp1 HG02293.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.808-1534G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012758 | |||||||
chr6:76012998 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0277 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.808-1774A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76012998 | |||||||
chr6:76013109 | G | T | 1 | a0009c0009t0001g0064 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.808-1885C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013109 | |||||||
chr6:76013294 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0061 others(125): Show |
129 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.808-2070G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013294 | |||||||
chr6:76013338 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.808-2114G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013338 | |||||||
chr6:76013469 | T | C | 1 | a0003c0003t0001g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.808-2245A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013469 | |||||||
chr6:76013698 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.808-2474A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013698 | |||||||
chr6:76013905 | C | T | 1 | a0002c0002t0001g0126 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.808-2681G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013905 | |||||||
chr6:76013980 | G | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.808-2756C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76013980 | |||||||
chr6:76014023 | G | A | 119 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0034 others(116): Show |
120 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.808-2799C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014023 | |||||||
chr6:76014218 | C | T | 1 | a0004c0004t0002g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.808-2994G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014218 | |||||||
chr6:76014285 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.808-3061G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014285 | |||||||
chr6:76014486 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.808-3262C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014486 | |||||||
chr6:76014838 | T | C | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.808-3614A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014838 | |||||||
chr6:76014967 | C | T | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.808-3743G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76014967 | |||||||
chr6:76015018 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.807+3700G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015018 | |||||||
chr6:76015459 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+3259C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015459 | |||||||
chr6:76015484 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+3234A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015484 | |||||||
chr6:76015487 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0230 others(3): Show |
6 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+3231C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015487 | |||||||
chr6:76015499 | C | T | 1 | a0003c0003t0001g0149 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.807+3219G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015499 | |||||||
chr6:76015534 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.807+3184G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015534 | |||||||
chr6:76015549 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.807+3169G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015549 | |||||||
chr6:76015567 | G | A | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.807+3151C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015567 | |||||||
chr6:76015598 | C | T | 6 | a0001c0001t0001g0095 a0002c0002t0001g0093 a0004c0004t0002g0088 others(3): Show |
6 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+3120G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015598 | |||||||
chr6:76015634 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+3084G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015634 | |||||||
chr6:76015753 | T | C | 1 | a0004c0004t0002g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.807+2965A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015753 | |||||||
chr6:76015800 | C | CA | 101 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(98): Show |
102 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.807+2917dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | |||||||
chr6:76015800 | C | CAA | 9 | a0001c0001t0001g0196 a0003c0003t0001g0029 a0003c0003t0001g0045 others(6): Show |
9 | HG00597.hp2 HG01169.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.807+2916_807+2917d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | |||||||
chr6:76015800 | CA | C | 96 | a0001c0001t0001g0021 a0001c0001t0001g0057 a0001c0001t0001g0091 others(93): Show |
96 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.807+2917delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | |||||||
chr6:76015800 | CAA | C | 11 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(8): Show |
11 | HG01099.hp1 HG02135.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.807+2916_807+2917d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | |||||||
chr6:76015800 | CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.807+2909_807+2917d others(11): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015800 | |||||||
chr6:76015892 | C | G | 131 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(128): Show |
132 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.807+2826G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015892 | |||||||
chr6:76015935 | T | TTC | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.807+2781_807+2782d others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76015935 | |||||||
chr6:76016025 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+2693T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016025 | |||||||
chr6:76016027 | C | G | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.807+2691G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016027 | |||||||
chr6:76016491 | T | C | 1 | a0005c0006t0003g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.807+2227A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016491 | |||||||
chr6:76016808 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.807+1910G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016808 | |||||||
chr6:76016928 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.807+1790G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016928 | |||||||
chr6:76016979 | G | A | 1 | a0007c0007t0004g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.807+1739C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76016979 | |||||||
chr6:76017195 | CA | C | 131 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(128): Show |
132 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.807+1522delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017195 | |||||||
chr6:76017370 | T | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.807+1348A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017370 | |||||||
chr6:76017437 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.807+1281G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017437 | |||||||
chr6:76017591 | C | T | 22 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0180 others(19): Show |
22 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.807+1127G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017591 | |||||||
chr6:76017898 | G | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.807+820C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017898 | |||||||
chr6:76017989 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.807+729G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76017989 | |||||||
chr6:76018020 | G | A | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.807+698C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018020 | |||||||
chr6:76018210 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+508T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018210 | |||||||
chr6:76018229 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+489G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018229 | |||||||
chr6:76018329 | C | T | 26 | a0001c0001t0001g0061 a0001c0018t0001g0262 a0002c0002t0001g0059 others(23): Show |
26 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.807+389G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018329 | |||||||
chr6:76018375 | A | G | 1 | a0006c0005t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.807+343T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018375 | |||||||
chr6:76018489 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.807+229C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018489 | |||||||
chr6:76018609 | A | T | 3 | a0005c0006t0003g0202 a0007c0007t0004g0001 a0007c0007t0004g0198 |
4 | HG01256.hp2 HG01258.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+109T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018609 | |||||||
chr6:76018618 | A | T | 1 | a0010c0010t0001g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.807+100T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018618 | |||||||
chr6:76018637 | C | T | 6 | a0003c0003t0006g0005 a0003c0003t0006g0006 a0007c0007t0004g0241 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.807+81G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018637 | |||||||
chr6:76018640 | C | T | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.807+78G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018640 | |||||||
chr6:76018641 | G | A | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.807+77C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018641 | |||||||
chr6:76018661 | G | A | 1 | a0009c0009t0001g0101 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.807+57C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 7/16 | chr6 | 76018661 | |||||||
chr6:76018866 | T | TA | 18 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.667-9dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76018866 | |||||||
chr6:76018866 | TA | T | 13 | a0001c0001t0001g0270 a0001c0001t0001g0284 a0002c0002t0001g0294 others(10): Show |
13 | HG00558.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.667-9delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76018866 | |||||||
chr6:76019240 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(25): Show |
29 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-382T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019240 | |||||||
chr6:76019332 | G | A | 1 | a0010c0010t0001g0278 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.667-474C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019332 | |||||||
chr6:76019402 | C | T | 3 | a0002c0002t0013g0007 a0007c0007t0004g0008 a0007c0007t0004g0090 |
3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.667-544G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019402 | |||||||
chr6:76019586 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.667-728G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019586 | |||||||
chr6:76019616 | G | A | 3 | a0002c0002t0013g0007 a0007c0007t0004g0008 a0007c0007t0004g0090 |
3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.667-758C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019616 | |||||||
chr6:76019822 | A | G | 9 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0230 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-964T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019822 | |||||||
chr6:76019867 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.667-1009T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019867 | |||||||
chr6:76019891 | A | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(13): Show |
16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.667-1033T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019891 | |||||||
chr6:76019949 | A | G | 2 | a0001c0001t0001g0163 a0009c0009t0001g0166 |
2 | NA18960.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.667-1091T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76019949 | |||||||
chr6:76020017 | A | G | 20 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0257 others(17): Show |
20 | HG01109.hp1 HG01884.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.667-1159T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020017 | |||||||
chr6:76020208 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.667-1350T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020208 | |||||||
chr6:76020257 | C | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.667-1399G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020257 | |||||||
chr6:76020337 | G | T | 1 | a0008c0008t0001g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.667-1479C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020337 | |||||||
chr6:76020476 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.667-1618C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020476 | |||||||
chr6:76020568 | C | T | 49 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0051 others(46): Show |
49 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.666+1548G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020568 | |||||||
chr6:76020698 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+1418C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020698 | |||||||
chr6:76020716 | A | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0271 |
2 | NA18959.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.666+1400T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020716 | |||||||
chr6:76020800 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.666+1316C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020800 | |||||||
chr6:76020997 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.666+1119G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76020997 | |||||||
chr6:76021004 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(275): Show |
280 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.666+1112T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021004 | |||||||
chr6:76021160 | G | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.666+956C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021160 | |||||||
chr6:76021479 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+637G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021479 | |||||||
chr6:76021480 | G | A | 12 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0230 others(9): Show |
12 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.666+636C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021480 | |||||||
chr6:76021641 | A | T | 2 | a0002c0002t0001g0296 a0002c0002t0001g0297 |
2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.666+475T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021641 | |||||||
chr6:76021665 | G | A | 3 | a0002c0002t0001g0230 a0003c0003t0001g0075 a0012c0012t0004g0229 |
3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.666+451C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021665 | |||||||
chr6:76021694 | T | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+422A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021694 | |||||||
chr6:76021725 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(161): Show |
165 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.666+391A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021725 | |||||||
chr6:76021751 | G | C | 8 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 others(5): Show |
8 | NA18947.hp1 NA18954.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.666+365C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021751 | |||||||
chr6:76021778 | C | CATATATA others(1): Show |
4 | a0002c0002t0001g0294 a0005c0006t0003g0227 a0015c0017t0001g0292 others(1): Show |
4 | HG01169.hp1 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+330_666+337dup others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(3): Show |
6 | a0001c0001t0005g0157 a0001c0026t0001g0251 a0007c0007t0004g0231 others(3): Show |
6 | HG01261.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+328_666+337dup others(10): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(5): Show |
16 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0225 others(13): Show |
16 | HG00438.hp2 HG02071.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.666+326_666+337dup others(12): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(7): Show |
46 | a0001c0001t0001g0095 a0001c0001t0001g0182 a0001c0001t0001g0189 others(43): Show |
47 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.666+324_666+337dup others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(9): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0023 others(42): Show |
46 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.666+322_666+337dup others(16): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(11): Show |
92 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0055 others(89): Show |
92 | HG00597.hp2 HG00609.hp2 HG01071.hp1 others(89): Show |
intron_variant | MODIFIER | c.666+320_666+337dup others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(13): Show |
76 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0031 others(73): Show |
76 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.666+318_666+337dup others(20): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(15): Show |
4 | a0001c0001t0001g0190 a0001c0001t0001g0275 a0002c0002t0001g0148 others(1): Show |
4 | HG01175.hp2 NA18947.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+316_666+337dup others(22): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(17): Show |
1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.666+314_666+337dup others(24): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(19): Show |
2 | a0002c0002t0001g0108 a0002c0002t0001g0184 |
2 | HG00738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.666+337_666+338ins others(26): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021778 | C | CATATATA others(23): Show |
2 | a0003c0003t0001g0022 a0008c0008t0001g0135 |
2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.666+337_666+338ins others(30): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021778 | |||||||
chr6:76021798 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.666+317_666+318ins others(18): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021798 | |||||||
chr6:76021853 | G | A | 1 | a0005c0006t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.666+263C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021853 | |||||||
chr6:76021869 | G | A | 1 | a0004c0004t0002g0054 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.666+247C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76021869 | |||||||
chr6:76022035 | T | C | 1 | a0009c0009t0001g0101 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.666+81A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 6/16 | chr6 | 76022035 | |||||||
chr6:76022297 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.563-78A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022297 | |||||||
chr6:76022364 | G | A | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.563-145C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022364 | |||||||
chr6:76022371 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.563-152A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022371 | |||||||
chr6:76022749 | G | A | 3 | a0002c0002t0013g0007 a0007c0007t0004g0008 a0007c0007t0004g0090 |
3 | HG01109.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.563-530C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022749 | |||||||
chr6:76022823 | A | G | 2 | a0001c0001t0001g0298 a0010c0010t0001g0299 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.563-604T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022823 | |||||||
chr6:76022892 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.563-673A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022892 | |||||||
chr6:76022995 | A | G | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0257 others(7): Show |
10 | HG02280.hp1 HG02559.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.563-776T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76022995 | |||||||
chr6:76023027 | A | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.563-808T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023027 | |||||||
chr6:76023121 | G | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.563-902C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023121 | |||||||
chr6:76023205 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.563-986C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023205 | |||||||
chr6:76023311 | A | G | 3 | a0001c0001t0001g0095 a0004c0004t0002g0094 a0004c0004t0002g0097 |
3 | HG00423.hp1 HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.563-1092T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023311 | |||||||
chr6:76023358 | G | C | 1 | a0003c0003t0001g0075 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-1139C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023358 | |||||||
chr6:76023410 | A | T | 4 | a0001c0016t0005g0014 a0001c0016t0005g0015 a0003c0015t0001g0012 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-1191T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023410 | |||||||
chr6:76023858 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.562+1336G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023858 | |||||||
chr6:76023920 | A | G | 115 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0034 others(112): Show |
116 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.562+1274T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023920 | |||||||
chr6:76023962 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0003c0003t0001g0083 |
3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.562+1232G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76023962 | |||||||
chr6:76024053 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.562+1141A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024053 | |||||||
chr6:76024173 | G | A | 16 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(13): Show |
16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.562+1021C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024173 | |||||||
chr6:76024205 | C | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.562+989G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024205 | |||||||
chr6:76024263 | A | G | 1 | a0008c0008t0001g0209 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.562+931T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024263 | |||||||
chr6:76024395 | C | CTTAGA | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(161): Show |
165 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.562+798_562+799ins others(5): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024395 | |||||||
chr6:76024398 | T | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(161): Show |
165 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.562+796A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024398 | |||||||
chr6:76024655 | TA | T | 15 | a0001c0001t0001g0217 a0005c0006t0003g0080 a0005c0006t0003g0081 others(12): Show |
16 | HG00140.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.562+538delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76024655 | |||||||
chr6:76025111 | A | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(13): Show |
16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.562+83T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76025111 | |||||||
chr6:76025119 | T | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(33): Show |
37 | HG00673.hp2 HG00741.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.562+75A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 5/16 | chr6 | 76025119 | |||||||
chr6:76025348 | A | G | 122 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0020 others(119): Show |
123 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.498-90T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025348 | |||||||
chr6:76025559 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(175): Show |
180 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.498-301C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025559 | |||||||
chr6:76025743 | T | C | 116 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0034 others(113): Show |
117 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.498-485A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025743 | |||||||
chr6:76025839 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.498-581A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76025839 | |||||||
chr6:76026035 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-777C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026035 | |||||||
chr6:76026040 | G | T | 1 | a0002c0002t0001g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.498-782C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026040 | |||||||
chr6:76026085 | ATGCGGGA others(21): Show |
A | 2 | a0002c0002t0001g0252 a0002c0002t0001g0261 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.498-855_498-828del others(28): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026085 | |||||||
chr6:76026116 | C | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0013g0007 others(3): Show |
6 | HG01109.hp1 HG02896.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-858G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026116 | |||||||
chr6:76026260 | C | A | 106 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0041 others(103): Show |
107 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.498-1002G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026260 | |||||||
chr6:76026306 | C | T | 2 | a0002c0002t0001g0248 a0002c0002t0001g0249 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.498-1048G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026306 | |||||||
chr6:76026336 | T | G | 1 | a0003c0003t0001g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.498-1078A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026336 | |||||||
chr6:76026387 | T | C | 1 | a0002c0002t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.498-1129A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026387 | |||||||
chr6:76026411 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.498-1153G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026411 | |||||||
chr6:76026434 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.498-1176G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026434 | |||||||
chr6:76026435 | T | A | 47 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0051 others(44): Show |
47 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.498-1177A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026435 | |||||||
chr6:76026451 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.498-1193G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026451 | |||||||
chr6:76026470 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-1212C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026470 | |||||||
chr6:76026527 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1269G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026527 | |||||||
chr6:76026612 | A | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.498-1354T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026612 | |||||||
chr6:76026712 | T | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1454A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026712 | |||||||
chr6:76026868 | G | A | 1 | a0010c0010t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.498-1610C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026868 | |||||||
chr6:76026932 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0084 others(23): Show |
27 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.498-1674A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76026932 | |||||||
chr6:76027112 | G | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1854C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027112 | |||||||
chr6:76027223 | G | C | 3 | a0005c0006t0003g0227 a0010c0010t0001g0199 a0011c0011t0003g0212 |
3 | HG01169.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.498-1965C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027223 | |||||||
chr6:76027277 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.498-2019A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027277 | |||||||
chr6:76027279 | T | C | 123 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0061 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.498-2021A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027279 | |||||||
chr6:76027280 | C | T | 4 | a0002c0002t0001g0078 a0002c0002t0001g0158 a0002c0002t0001g0285 others(1): Show |
4 | HG02273.hp2 HG03017.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-2022G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027280 | |||||||
chr6:76027445 | T | C | 1 | a0001c0001t0005g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.498-2187A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027445 | |||||||
chr6:76027655 | C | G | 1 | a0001c0001t0001g0274 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.498-2397G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027655 | |||||||
chr6:76027696 | G | A | 16 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(13): Show |
16 | HG01109.hp1 HG02145.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.498-2438C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027696 | |||||||
chr6:76027790 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2532C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027790 | |||||||
chr6:76027854 | T | G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(13): Show |
16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.498-2596A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027854 | |||||||
chr6:76027990 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2732C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76027990 | |||||||
chr6:76028033 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2775G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028033 | |||||||
chr6:76028256 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2998G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028256 | |||||||
chr6:76028288 | G | T | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.498-3030C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028288 | |||||||
chr6:76028339 | T | C | 72 | a0001c0001t0001g0091 a0001c0001t0001g0130 a0001c0001t0001g0153 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.498-3081A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028339 | |||||||
chr6:76028395 | C | T | 1 | a0008c0008t0001g0119 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.498-3137G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028395 | |||||||
chr6:76028396 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.498-3138C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028396 | |||||||
chr6:76028416 | G | A | 2 | a0020c0024t0001g0132 a0024c0022t0001g0050 |
2 | NA18946.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.498-3158C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028416 | |||||||
chr6:76028570 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-3312G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028570 | |||||||
chr6:76028595 | C | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(13): Show |
16 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.498-3337G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028595 | |||||||
chr6:76028596 | G | A | 1 | a0002c0002t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.498-3338C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028596 | |||||||
chr6:76028656 | C | T | 8 | a0001c0016t0005g0014 a0001c0016t0005g0015 a0002c0002t0001g0294 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.498-3398G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028656 | |||||||
chr6:76028657 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.498-3399C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028657 | |||||||
chr6:76028900 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0259 others(7): Show |
10 | HG02145.hp1 HG02293.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-3642G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028900 | |||||||
chr6:76028916 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-3658G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028916 | |||||||
chr6:76028972 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0265 others(20): Show |
24 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.498-3714G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76028972 | |||||||
chr6:76029249 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498-3991C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029249 | |||||||
chr6:76029302 | G | A | 1 | a0002c0002t0001g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.498-4044C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029302 | |||||||
chr6:76029438 | G | T | 27 | a0001c0001t0001g0095 a0001c0001t0001g0163 a0002c0002t0001g0093 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.498-4180C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029438 | |||||||
chr6:76029701 | G | T | 1 | a0002c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.498-4443C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029701 | |||||||
chr6:76029763 | C | G | 2 | a0007c0007t0004g0219 a0007c0007t0004g0228 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.498-4505G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76029763 | |||||||
chr6:76030095 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.497+4220A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030095 | |||||||
chr6:76030123 | T | C | 1 | a0002c0002t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+4192A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030123 | |||||||
chr6:76030178 | A | G | 1 | a0010c0010t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.497+4137T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030178 | |||||||
chr6:76030179 | C | G | 1 | a0010c0010t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.497+4136G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030179 | |||||||
chr6:76030185 | G | A | 1 | a0002c0002t0007g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497+4130C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030185 | |||||||
chr6:76030462 | TA | T | 3 | a0002c0002t0001g0230 a0003c0003t0001g0075 a0012c0012t0004g0229 |
3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.497+3852delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030462 | |||||||
chr6:76030553 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+3762C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030553 | |||||||
chr6:76030657 | A | C | 108 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0130 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.497+3658T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030657 | |||||||
chr6:76030780 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.497+3535A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030780 | |||||||
chr6:76030782 | G | A | 11 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(8): Show |
11 | HG02055.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.497+3533C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030782 | |||||||
chr6:76030932 | C | T | 4 | a0001c0001t0001g0270 a0001c0001t0001g0286 a0003c0003t0001g0269 others(1): Show |
4 | HG01175.hp1 HG01358.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+3383G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030932 | |||||||
chr6:76030964 | C | T | 3 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0006c0005t0008g0087 |
3 | HG00738.hp1 HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.497+3351G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030964 | |||||||
chr6:76030996 | C | T | 1 | a0001c0001t0005g0223 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497+3319G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76030996 | |||||||
chr6:76031100 | T | C | 1 | a0006c0005t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.497+3215A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031100 | |||||||
chr6:76031111 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+3204G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031111 | |||||||
chr6:76031202 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+3113T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031202 | |||||||
chr6:76031203 | T | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+3112A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031203 | |||||||
chr6:76031225 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0265 others(20): Show |
24 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.497+3090A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031225 | |||||||
chr6:76031342 | T | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0052 others(15): Show |
18 | HG00621.hp1 HG02027.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.497+2973A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031342 | |||||||
chr6:76031342 | T | G | 3 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 |
3 | NA18981.hp1 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.497+2973A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031342 | |||||||
chr6:76031734 | C | T | 2 | a0012c0012t0004g0161 a0012c0012t0004g0162 |
2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.497+2581G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031734 | |||||||
chr6:76031861 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0005g0010 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.497+2454A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031861 | |||||||
chr6:76031986 | T | A | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.497+2329A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031986 | |||||||
chr6:76031992 | C | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.497+2323G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76031992 | |||||||
chr6:76032260 | T | G | 5 | a0001c0016t0005g0014 a0001c0016t0005g0015 a0003c0015t0001g0012 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+2055A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032260 | |||||||
chr6:76032309 | AT | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.497+2005delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032309 | |||||||
chr6:76032467 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0005g0010 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.497+1848C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032467 | |||||||
chr6:76032543 | A | G | 3 | a0003c0015t0001g0012 a0003c0015t0001g0013 a0006c0005t0006g0221 |
3 | HG01109.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.497+1772T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032543 | |||||||
chr6:76032875 | T | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+1440A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032875 | |||||||
chr6:76032938 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.497+1377G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76032938 | |||||||
chr6:76033002 | C | G | 1 | a0010c0010t0001g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.497+1313G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033002 | |||||||
chr6:76033205 | C | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.497+1110G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033205 | |||||||
chr6:76033367 | C | T | 5 | a0003c0003t0008g0133 a0003c0003t0008g0177 a0003c0003t0014g0079 others(2): Show |
5 | HG00741.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+948G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033367 | |||||||
chr6:76033399 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497+916T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033399 | |||||||
chr6:76033770 | CTCT | C | 5 | a0001c0016t0005g0014 a0001c0016t0005g0015 a0003c0015t0001g0012 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+542_497+544del others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033770 | |||||||
chr6:76033848 | G | A | 2 | a0001c0001t0005g0222 a0001c0001t0005g0223 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.497+467C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033848 | |||||||
chr6:76033896 | T | A | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+419A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033896 | |||||||
chr6:76033943 | G | T | 2 | a0001c0001t0001g0298 a0010c0010t0001g0299 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.497+372C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76033943 | |||||||
chr6:76034142 | T | C | 1 | a0003c0003t0001g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.497+173A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76034142 | |||||||
chr6:76034264 | T | G | 3 | a0003c0015t0001g0012 a0003c0015t0001g0013 a0006c0005t0006g0221 |
3 | HG01109.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.497+51A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 4/16 | chr6 | 76034264 | |||||||
chr6:76034395 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0003c0003t0001g0083 |
3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.469-52C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 3/16 | chr6 | 76034395 | |||||||
chr6:76034576 | C | A | 3 | a0002c0002t0001g0230 a0003c0003t0001g0075 a0012c0012t0004g0229 |
3 | HG02559.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.468+45G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 3/16 | chr6 | 76034576 | |||||||
chr6:76034581 | C | T | 56 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0095 others(53): Show |
57 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.468+40G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 3/16 | chr6 | 76034581 | |||||||
chr6:76034831 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(29): Show |
32 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.302-44G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034831 | |||||||
chr6:76034839 | A | C | 1 | a0002c0002t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.302-52T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034839 | |||||||
chr6:76034887 | C | T | 1 | a0003c0003t0001g0029 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.302-100G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034887 | |||||||
chr6:76034892 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.302-105G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76034892 | |||||||
chr6:76035033 | C | T | 115 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0061 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-246G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035033 | |||||||
chr6:76035217 | C | T | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.302-430G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035217 | |||||||
chr6:76035238 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.302-451T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035238 | |||||||
chr6:76035274 | G | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.302-487C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035274 | |||||||
chr6:76035277 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.302-490G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035277 | |||||||
chr6:76035346 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.302-559T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035346 | |||||||
chr6:76035360 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0005g0010 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.302-573C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035360 | |||||||
chr6:76035447 | C | T | 3 | a0007c0007t0004g0242 a0007c0007t0004g0243 a0007c0007t0004g0244 |
3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.302-660G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035447 | |||||||
chr6:76035499 | C | CA | 16 | a0001c0001t0001g0237 a0001c0001t0001g0259 a0001c0001t0001g0263 others(13): Show |
16 | HG02293.hp2 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.302-713dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035499 | |||||||
chr6:76035499 | CA | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(136): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.302-713delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035499 | |||||||
chr6:76035499 | CAA | C | 106 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0130 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.302-714_302-713del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035499 | |||||||
chr6:76035529 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.302-742T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035529 | |||||||
chr6:76035535 | G | A | 2 | a0002c0002t0001g0147 a0002c0002t0005g0076 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.302-748C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035535 | |||||||
chr6:76035623 | C | T | 1 | a0003c0003t0002g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.302-836G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035623 | |||||||
chr6:76035635 | A | G | 1 | a0004c0004t0002g0054 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.302-848T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035635 | |||||||
chr6:76035734 | A | C | 1 | a0001c0001t0005g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.302-947T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035734 | |||||||
chr6:76035740 | C | G | 1 | a0002c0002t0001g0285 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-953G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035740 | |||||||
chr6:76035774 | C | G | 1 | a0002c0002t0001g0285 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-987G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035774 | |||||||
chr6:76035830 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.302-1043C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035830 | |||||||
chr6:76035853 | G | A | 1 | a0008c0008t0001g0197 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302-1066C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76035853 | |||||||
chr6:76036222 | A | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
16 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.302-1435T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036222 | |||||||
chr6:76036278 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.302-1491G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036278 | |||||||
chr6:76036334 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.302-1547G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036334 | |||||||
chr6:76036686 | T | C | 5 | a0002c0002t0001g0134 a0002c0002t0001g0195 a0002c0002t0001g0211 others(2): Show |
5 | HG00735.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-1899A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036686 | |||||||
chr6:76036787 | GAGTGGCT others(72): Show |
G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.302-2079_302-2001d others(81): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036787 | |||||||
chr6:76036828 | C | T | 2 | a0003c0003t0001g0030 a0003c0003t0001g0103 |
2 | HG00738.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.302-2041G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036828 | |||||||
chr6:76036909 | A | C | 26 | a0001c0001t0001g0061 a0001c0018t0001g0262 a0002c0002t0001g0059 others(23): Show |
26 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.302-2122T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036909 | |||||||
chr6:76036944 | A | G | 2 | a0002c0002t0001g0296 a0002c0002t0001g0297 |
2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.302-2157T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76036944 | |||||||
chr6:76037021 | T | C | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.302-2234A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037021 | |||||||
chr6:76037068 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.302-2281C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037068 | |||||||
chr6:76037233 | G | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(159): Show |
162 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.302-2446C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037233 | |||||||
chr6:76037761 | A | G | 1 | a0005c0006t0003g0218 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.302-2974T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037761 | |||||||
chr6:76037853 | C | T | 1 | a0012c0012t0004g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.302-3066G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037853 | |||||||
chr6:76037866 | A | T | 1 | a0002c0002t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.302-3079T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037866 | |||||||
chr6:76037914 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.302-3127A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037914 | |||||||
chr6:76037927 | C | A | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(293): Show |
intron_variant | MODIFIER | c.302-3140G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037927 | |||||||
chr6:76037948 | T | A | 2 | a0001c0001t0001g0190 a0003c0003t0001g0191 |
2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.302-3161A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037948 | |||||||
chr6:76037957 | T | C | 1 | a0002c0002t0001g0108 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.302-3170A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76037957 | |||||||
chr6:76038045 | C | T | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(291): Show |
296 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(293): Show |
intron_variant | MODIFIER | c.302-3258G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038045 | |||||||
chr6:76038106 | A | G | 2 | a0008c0008t0001g0214 a0008c0008t0001g0215 |
2 | NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.302-3319T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038106 | |||||||
chr6:76038179 | G | A | 2 | a0002c0002t0001g0155 a0006c0005t0001g0154 |
2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.302-3392C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038179 | |||||||
chr6:76038227 | A | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(187): Show |
191 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.302-3440T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038227 | |||||||
chr6:76038476 | G | A | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.301+3417C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038476 | |||||||
chr6:76038753 | C | T | 1 | a0006c0005t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.301+3140G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038753 | |||||||
chr6:76038828 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.301+3065G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76038828 | |||||||
chr6:76039098 | C | T | 1 | a0017c0028t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301+2795G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039098 | |||||||
chr6:76039356 | G | GT | 42 | a0001c0001t0001g0011 a0001c0001t0001g0095 a0001c0001t0001g0180 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+2536dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039356 | |||||||
chr6:76039356 | GT | G | 103 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(100): Show |
103 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.301+2536delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039356 | |||||||
chr6:76039365 | T | C | 2 | a0001c0001t0005g0222 a0001c0001t0005g0223 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301+2528A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039365 | |||||||
chr6:76039402 | A | C | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.301+2491T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039402 | |||||||
chr6:76039501 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(1): Show |
4 | NA18941.hp2 NA18974.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+2392C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039501 | |||||||
chr6:76039542 | G | A | 3 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 |
3 | NA18981.hp1 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.301+2351C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039542 | |||||||
chr6:76039750 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.301+2143G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039750 | |||||||
chr6:76039909 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.301+1984T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039909 | |||||||
chr6:76039955 | T | G | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+1938A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76039955 | |||||||
chr6:76040168 | T | G | 1 | a0002c0002t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.301+1725A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040168 | |||||||
chr6:76040184 | A | G | 1 | a0011c0011t0003g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301+1709T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040184 | |||||||
chr6:76040196 | A | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.301+1697T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040196 | |||||||
chr6:76040412 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.301+1481A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040412 | |||||||
chr6:76040674 | C | G | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.301+1219G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040674 | |||||||
chr6:76040871 | T | C | 2 | a0012c0012t0004g0161 a0012c0012t0004g0162 |
2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.301+1022A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040871 | |||||||
chr6:76040971 | G | T | 2 | a0002c0002t0001g0290 a0006c0005t0001g0139 |
2 | HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.301+922C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76040971 | |||||||
chr6:76041028 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(22): Show |
26 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.301+865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041028 | |||||||
chr6:76041042 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.301+851C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041042 | |||||||
chr6:76041137 | T | C | 1 | a0006c0005t0008g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.301+756A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041137 | |||||||
chr6:76041163 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(14): Show |
17 | HG00597.hp1 HG00609.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.301+730C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041163 | |||||||
chr6:76041243 | T | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0237 others(18): Show |
21 | HG01109.hp1 HG02145.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.301+650A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041243 | |||||||
chr6:76041312 | A | AACC | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.301+578_301+580dup others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041312 | |||||||
chr6:76041356 | A | G | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+537T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041356 | |||||||
chr6:76041496 | T | A | 1 | a0003c0003t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.301+397A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 2/16 | chr6 | 76041496 | |||||||
chr6:76042175 | A | G | 5 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(2): Show |
5 | HG02293.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-49T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042175 | |||||||
chr6:76042329 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-203C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042329 | |||||||
chr6:76042346 | A | G | 1 | a0003c0003t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-220T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042346 | |||||||
chr6:76042449 | G | C | 1 | a0001c0001t0005g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-323C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042449 | |||||||
chr6:76042608 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(22): Show |
26 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-482T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042608 | |||||||
chr6:76042943 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-817G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042943 | |||||||
chr6:76042960 | A | C | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-834T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76042960 | |||||||
chr6:76043184 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.68-1058G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043184 | |||||||
chr6:76043215 | T | A | 85 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.68-1089A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043215 | |||||||
chr6:76043269 | G | A | 6 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0247 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1143C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043269 | |||||||
chr6:76043308 | G | T | 1 | a0002c0002t0001g0285 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.68-1182C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043308 | |||||||
chr6:76043384 | G | T | 1 | a0004c0004t0002g0071 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.68-1258C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043384 | |||||||
chr6:76043481 | GT | G | 123 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.68-1356delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043481 | |||||||
chr6:76043517 | A | G | 1 | a0009c0009t0001g0064 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.68-1391T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043517 | |||||||
chr6:76043563 | C | T | 1 | a0002c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.68-1437G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043563 | |||||||
chr6:76043595 | T | C | 116 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(113): Show |
116 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.68-1469A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043595 | |||||||
chr6:76043736 | A | G | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-1610T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043736 | |||||||
chr6:76043897 | G | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0237 others(18): Show |
21 | HG01109.hp1 HG02145.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.68-1771C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043897 | |||||||
chr6:76043921 | A | G | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-1795T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043921 | |||||||
chr6:76043940 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-1814G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043940 | |||||||
chr6:76043971 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-1845G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76043971 | |||||||
chr6:76044087 | A | C | 4 | a0001c0016t0005g0014 a0001c0016t0005g0015 a0003c0015t0001g0012 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1961T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044087 | |||||||
chr6:76044094 | C | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.68-1968G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044094 | |||||||
chr6:76044272 | A | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2146T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044272 | |||||||
chr6:76044548 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.68-2422A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044548 | |||||||
chr6:76044897 | C | G | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2771G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76044897 | |||||||
chr6:76045024 | C | T | 4 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(1): Show |
4 | HG02647.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2898G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045024 | |||||||
chr6:76045065 | T | C | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2939A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045065 | |||||||
chr6:76045259 | C | T | 23 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(20): Show |
23 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-3133G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045259 | |||||||
chr6:76045344 | G | A | 2 | a0001c0001t0005g0157 a0005c0006t0003g0086 |
2 | HG00140.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-3218C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045344 | |||||||
chr6:76045418 | T | C | 2 | a0004c0004t0002g0240 a0009c0009t0001g0111 |
2 | NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.68-3292A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045418 | |||||||
chr6:76045441 | C | CT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(84): Show |
88 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.68-3316dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045441 | |||||||
chr6:76045441 | C | CTT | 83 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.68-3317_68-3316dup others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045441 | |||||||
chr6:76045479 | G | A | 1 | a0025c0027t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-3353C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045479 | |||||||
chr6:76045504 | G | A | 112 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.68-3378C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045504 | |||||||
chr6:76045604 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.68-3478A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045604 | |||||||
chr6:76045994 | A | C | 1 | a0001c0001t0005g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.68-3868T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76045994 | |||||||
chr6:76046090 | GA | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0020 others(151): Show |
156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.68-3965delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046090 | |||||||
chr6:76046186 | C | T | 1 | a0011c0011t0003g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-4060G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046186 | |||||||
chr6:76046279 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-4153C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046279 | |||||||
chr6:76046305 | GA | G | 76 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0070 others(73): Show |
76 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.68-4180delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046305 | |||||||
chr6:76046320 | G | A | 4 | a0002c0002t0001g0226 a0002c0002t0001g0294 a0015c0017t0001g0292 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-4194C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046320 | |||||||
chr6:76046472 | G | A | 1 | a0002c0002t0001g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.68-4346C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046472 | |||||||
chr6:76046519 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.68-4393A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046519 | |||||||
chr6:76046529 | A | G | 3 | a0002c0002t0001g0226 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-4403T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046529 | |||||||
chr6:76046531 | G | T | 4 | a0002c0002t0001g0226 a0002c0002t0001g0294 a0015c0017t0001g0292 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-4405C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046531 | |||||||
chr6:76046657 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.68-4531T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046657 | |||||||
chr6:76046678 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-4552G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046678 | |||||||
chr6:76046706 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
16 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-4580G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046706 | |||||||
chr6:76046782 | G | A | 1 | a0003c0003t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-4656C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046782 | |||||||
chr6:76046811 | C | T | 2 | a0001c0001t0001g0084 a0003c0003t0001g0083 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68-4685G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046811 | |||||||
chr6:76046812 | G | A | 2 | a0002c0002t0001g0150 a0003c0003t0001g0149 |
2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.68-4686C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046812 | |||||||
chr6:76046991 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-4865T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76046991 | |||||||
chr6:76047132 | T | C | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-5006A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047132 | |||||||
chr6:76047214 | C | T | 38 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(35): Show |
38 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.68-5088G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047214 | |||||||
chr6:76047249 | G | A | 1 | a0003c0003t0006g0006 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68-5123C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047249 | |||||||
chr6:76047631 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-5505G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047631 | |||||||
chr6:76047674 | TATTA | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-5552_68-5549del others(4): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047674 | |||||||
chr6:76047723 | T | C | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68-5597A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047723 | |||||||
chr6:76047895 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0237 others(2): Show |
5 | HG02896.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-5769G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76047895 | |||||||
chr6:76048037 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(250): Show |
255 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.68-5911C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048037 | |||||||
chr6:76048141 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-6015C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048141 | |||||||
chr6:76048270 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
18 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-6144T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048270 | |||||||
chr6:76048362 | A | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6236T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048362 | |||||||
chr6:76048363 | G | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6237C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048363 | |||||||
chr6:76048381 | C | T | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-6255G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048381 | |||||||
chr6:76048382 | A | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6256T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048382 | |||||||
chr6:76048460 | C | A | 1 | a0005c0006t0003g0266 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.68-6334G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048460 | |||||||
chr6:76048461 | G | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(10): Show |
13 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-6335C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048461 | |||||||
chr6:76048509 | G | T | 214 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.68-6383C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048509 | |||||||
chr6:76048556 | C | T | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-6430G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048556 | |||||||
chr6:76048581 | A | T | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-6455T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048581 | |||||||
chr6:76048662 | G | A | 7 | a0001c0001t0001g0153 a0003c0003t0001g0066 a0003c0003t0001g0067 others(4): Show |
7 | HG01081.hp2 HG01099.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-6536C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76048662 | |||||||
chr6:76049001 | T | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6875A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049001 | |||||||
chr6:76049046 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-6920G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049046 | |||||||
chr6:76049088 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(294): Show |
299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.68-6962G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049088 | |||||||
chr6:76049110 | A | C | 1 | a0010c0010t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68-6984T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049110 | |||||||
chr6:76049122 | A | G | 1 | a0005c0006t0003g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.68-6996T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049122 | |||||||
chr6:76049190 | A | G | 111 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0084 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.68-7064T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049190 | |||||||
chr6:76049308 | A | G | 216 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(213): Show |
217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.68-7182T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049308 | |||||||
chr6:76049410 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.68-7284C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049410 | |||||||
chr6:76049462 | TTCTCTCT others(7): Show |
T | 2 | a0001c0001t0001g0256 a0002c0002t0007g0255 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.68-7350_68-7337del others(14): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049462 | |||||||
chr6:76049482 | C | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.68-7356G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049482 | |||||||
chr6:76049590 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.68-7464G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049590 | |||||||
chr6:76049608 | A | G | 5 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0005c0006t0003g0106 others(2): Show |
5 | HG00738.hp1 HG01496.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-7482T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049608 | |||||||
chr6:76049666 | G | A | 1 | a0011c0011t0003g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.68-7540C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049666 | |||||||
chr6:76049695 | A | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 |
3 | HG02622.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-7569T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049695 | |||||||
chr6:76049822 | A | G | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7696T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049822 | |||||||
chr6:76049870 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.68-7744G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76049870 | |||||||
chr6:76050229 | C | A | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8103G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050229 | |||||||
chr6:76050312 | G | A | 1 | a0003c0003t0001g0030 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.68-8186C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050312 | |||||||
chr6:76050317 | C | T | 9 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0247 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-8191G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050317 | |||||||
chr6:76050325 | C | A | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-8199G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050325 | |||||||
chr6:76050350 | T | G | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-8224A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050350 | |||||||
chr6:76050357 | C | T | 9 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0247 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-8231G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050357 | |||||||
chr6:76050358 | G | A | 5 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0237 others(2): Show |
5 | HG02896.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-8232C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050358 | |||||||
chr6:76050397 | C | T | 1 | a0003c0003t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-8271G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050397 | |||||||
chr6:76050398 | G | A | 2 | a0002c0002t0001g0164 a0004c0004t0002g0036 |
2 | NA18944.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.68-8272C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050398 | |||||||
chr6:76050408 | A | T | 1 | a0004c0004t0002g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.68-8282T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050408 | |||||||
chr6:76050440 | CA | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0259 a0001c0001t0001g0263 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-8315delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050440 | |||||||
chr6:76050588 | C | T | 110 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(107): Show |
111 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.68-8462G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050588 | |||||||
chr6:76050678 | G | A | 2 | a0002c0002t0001g0155 a0006c0005t0001g0154 |
2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.68-8552C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050678 | |||||||
chr6:76050726 | C | T | 2 | a0003c0015t0001g0012 a0003c0015t0001g0013 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.68-8600G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050726 | |||||||
chr6:76050956 | G | A | 2 | a0001c0016t0005g0014 a0001c0016t0005g0015 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.68-8830C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050956 | |||||||
chr6:76050959 | G | A | 1 | a0003c0003t0001g0156 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.68-8833C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050959 | |||||||
chr6:76050994 | C | T | 2 | a0002c0002t0001g0252 a0002c0002t0001g0261 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-8868G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050994 | |||||||
chr6:76050999 | A | G | 1 | a0002c0002t0001g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.68-8873T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76050999 | |||||||
chr6:76051072 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(10): Show |
13 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-8946A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051072 | |||||||
chr6:76051192 | T | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-9066A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051192 | |||||||
chr6:76051225 | C | T | 1 | a0007c0007t0004g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.68-9099G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051225 | |||||||
chr6:76051406 | C | G | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-9280G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051406 | |||||||
chr6:76051444 | T | C | 1 | a0001c0001t0005g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-9318A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051444 | |||||||
chr6:76051536 | A | G | 2 | a0002c0002t0001g0252 a0002c0002t0001g0261 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-9410T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051536 | |||||||
chr6:76051983 | G | GA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0259 a0001c0001t0001g0263 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-9858dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76051983 | |||||||
chr6:76052000 | A | G | 1 | a0025c0027t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-9874T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052000 | |||||||
chr6:76052247 | T | A | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10121A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052247 | |||||||
chr6:76052249 | T | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10123A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052249 | |||||||
chr6:76052291 | T | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10165A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052291 | |||||||
chr6:76052411 | C | G | 6 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-10285G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052411 | |||||||
chr6:76052743 | G | A | 258 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.68-10617C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052743 | |||||||
chr6:76052843 | G | A | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10717C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052843 | |||||||
chr6:76052844 | A | T | 1 | a0013c0013t0001g0181 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.68-10718T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052844 | |||||||
chr6:76052965 | T | C | 2 | a0001c0001t0005g0238 a0001c0001t0005g0239 |
2 | HG02293.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.68-10839A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76052965 | |||||||
chr6:76053149 | A | G | 1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.68-11023T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053149 | |||||||
chr6:76053232 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.68-11106G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053232 | |||||||
chr6:76053612 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-11486G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053612 | |||||||
chr6:76053673 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-11547T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053673 | |||||||
chr6:76053724 | T | C | 1 | a0003c0003t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-11598A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76053724 | |||||||
chr6:76054179 | T | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-12053A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054179 | |||||||
chr6:76054315 | T | C | 3 | a0001c0001t0001g0213 a0008c0008t0001g0214 a0008c0008t0001g0215 |
3 | HG00423.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.68-12189A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054315 | |||||||
chr6:76054456 | T | C | 1 | a0002c0002t0001g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.68-12330A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054456 | |||||||
chr6:76054473 | T | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-12347A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054473 | |||||||
chr6:76054474 | T | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-12348A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054474 | |||||||
chr6:76054596 | T | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-12470A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054596 | |||||||
chr6:76054602 | A | T | 1 | a0007c0007t0004g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.68-12476T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054602 | |||||||
chr6:76054673 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-12547T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054673 | |||||||
chr6:76054839 | A | ACAAAGG | 85 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-12719_68-12714d others(8): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054839 | |||||||
chr6:76054858 | G | T | 85 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-12732C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76054858 | |||||||
chr6:76055136 | G | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.68-13010C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055136 | |||||||
chr6:76055214 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.68-13088A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055214 | |||||||
chr6:76055349 | A | G | 85 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-13223T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055349 | |||||||
chr6:76055399 | T | C | 261 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(258): Show |
262 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.68-13273A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055399 | |||||||
chr6:76055550 | CA | C | 125 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.68-13425delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055550 | |||||||
chr6:76055623 | G | A | 7 | a0001c0001t0005g0157 a0002c0002t0001g0078 a0002c0002t0001g0158 others(4): Show |
7 | HG00140.hp1 HG00741.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-13497C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055623 | |||||||
chr6:76055675 | A | AAGAAG | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-13554_68-13550d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055675 | |||||||
chr6:76055759 | A | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(34): Show |
37 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.68-13633T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055759 | |||||||
chr6:76055855 | C | T | 1 | a0008c0008t0001g0197 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.68-13729G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76055855 | |||||||
chr6:76056050 | C | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-13924G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056050 | |||||||
chr6:76056051 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.68-13925C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056051 | |||||||
chr6:76056083 | G | GA | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-13958dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056083 | |||||||
chr6:76056219 | G | T | 1 | a0002c0002t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.68-14093C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056219 | |||||||
chr6:76056283 | G | A | 2 | a0005c0006t0003g0081 a0005c0006t0003g0086 |
2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.68-14157C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056283 | |||||||
chr6:76056502 | C | CA | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-14377dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056502 | |||||||
chr6:76056588 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.68-14462T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056588 | |||||||
chr6:76056644 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.68-14518G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056644 | |||||||
chr6:76056652 | A | G | 1 | a0002c0002t0001g0195 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.68-14526T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056652 | |||||||
chr6:76056683 | T | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-14557A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056683 | |||||||
chr6:76056719 | C | A | 1 | a0001c0001t0005g0223 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68-14593G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056719 | |||||||
chr6:76056790 | A | T | 126 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.68-14664T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056790 | |||||||
chr6:76056945 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-14819G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76056945 | |||||||
chr6:76057010 | C | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-14884G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057010 | |||||||
chr6:76057117 | G | A | 4 | a0001c0001t0005g0238 a0001c0001t0005g0239 a0003c0003t0001g0160 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-14991C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057117 | |||||||
chr6:76057138 | G | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-15012C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057138 | |||||||
chr6:76057262 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18941.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.68-15136T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057262 | |||||||
chr6:76057270 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-15144A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057270 | |||||||
chr6:76057379 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.67+15043C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057379 | |||||||
chr6:76057393 | C | G | 2 | a0001c0001t0005g0238 a0001c0001t0005g0239 |
2 | HG02293.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.67+15029G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057393 | |||||||
chr6:76057447 | A | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14975T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057447 | |||||||
chr6:76057475 | C | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14947G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057475 | |||||||
chr6:76057507 | G | A | 210 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.67+14915C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057507 | |||||||
chr6:76057536 | A | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14886T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057536 | |||||||
chr6:76057619 | C | T | 1 | a0003c0003t0001g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.67+14803G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057619 | |||||||
chr6:76057641 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.67+14781T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057641 | |||||||
chr6:76057741 | T | C | 126 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.67+14681A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057741 | |||||||
chr6:76057969 | A | AAAAAT | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+14448_67+14452d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057969 | |||||||
chr6:76057969 | AAAAAT | A | 210 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.67+14448_67+14452d others(7): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76057969 | |||||||
chr6:76058075 | A | C | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0007g0255 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+14347T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058075 | |||||||
chr6:76058093 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(12): Show |
15 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+14329T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058093 | |||||||
chr6:76058107 | A | T | 2 | a0004c0004t0002g0088 a0006c0005t0002g0089 |
2 | NA18955.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67+14315T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058107 | |||||||
chr6:76058279 | A | C | 1 | a0006c0005t0008g0087 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67+14143T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058279 | |||||||
chr6:76058367 | T | C | 3 | a0005c0006t0003g0218 a0007c0007t0004g0219 a0007c0007t0004g0228 |
3 | HG01070.hp2 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.67+14055A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058367 | |||||||
chr6:76058542 | C | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(241): Show |
246 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.67+13880G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058542 | |||||||
chr6:76058784 | A | G | 3 | a0009c0009t0001g0253 a0009c0009t0001g0258 a0009c0009t0007g0254 |
3 | HG02280.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+13638T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058784 | |||||||
chr6:76058804 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0007g0255 |
3 | HG02615.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67+13618A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058804 | |||||||
chr6:76058829 | T | G | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0007g0255 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+13593A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76058829 | |||||||
chr6:76059295 | A | C | 4 | a0001c0018t0001g0262 a0002c0002t0001g0294 a0015c0017t0001g0292 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+13127T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059295 | |||||||
chr6:76059322 | A | G | 1 | a0005c0006t0003g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.67+13100T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059322 | |||||||
chr6:76059331 | G | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+13091C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059331 | |||||||
chr6:76059357 | A | T | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0007g0255 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+13065T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059357 | |||||||
chr6:76059402 | C | CT | 127 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+13019dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059402 | |||||||
chr6:76059402 | CT | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+13019delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059402 | |||||||
chr6:76059415 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.67+13007C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059415 | |||||||
chr6:76059439 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.67+12983C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059439 | |||||||
chr6:76059465 | G | A | 2 | a0012c0012t0004g0161 a0012c0012t0004g0162 |
2 | HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.67+12957C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059465 | |||||||
chr6:76059481 | T | C | 2 | a0002c0002t0001g0288 a0002c0002t0001g0289 |
2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.67+12941A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059481 | |||||||
chr6:76059585 | A | G | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12837T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059585 | |||||||
chr6:76059680 | C | A | 4 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12742G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059680 | |||||||
chr6:76059768 | A | T | 4 | a0001c0018t0001g0262 a0002c0002t0001g0294 a0015c0017t0001g0292 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12654T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059768 | |||||||
chr6:76059993 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.67+12429A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76059993 | |||||||
chr6:76060002 | T | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+12420A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060002 | |||||||
chr6:76060195 | A | G | 2 | a0003c0003t0001g0232 a0004c0004t0001g0233 |
2 | NA18987.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.67+12227T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060195 | |||||||
chr6:76060349 | G | A | 4 | a0001c0001t0005g0220 a0001c0001t0005g0222 a0001c0001t0005g0223 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12073C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060349 | |||||||
chr6:76060403 | A | T | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+12019T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060403 | |||||||
chr6:76060528 | C | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+11894G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060528 | |||||||
chr6:76060543 | A | G | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+11879T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060543 | |||||||
chr6:76060784 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
20 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11638C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060784 | |||||||
chr6:76060850 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+11572C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76060850 | |||||||
chr6:76061080 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0003c0003t0001g0083 |
3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.67+11342G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061080 | |||||||
chr6:76061208 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+11214T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061208 | |||||||
chr6:76061256 | A | G | 216 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(213): Show |
217 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.67+11166T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061256 | |||||||
chr6:76061316 | A | G | 1 | a0002c0002t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+11106T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061316 | |||||||
chr6:76061418 | C | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+11004G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061418 | |||||||
chr6:76061581 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0003c0003t0001g0022 |
3 | HG01928.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.67+10841G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061581 | |||||||
chr6:76061635 | A | G | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+10787T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061635 | |||||||
chr6:76061643 | T | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10779A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061643 | |||||||
chr6:76061689 | G | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10733C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061689 | |||||||
chr6:76061722 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+10700T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061722 | |||||||
chr6:76061737 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.67+10685G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061737 | |||||||
chr6:76061861 | T | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+10561A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061861 | |||||||
chr6:76061862 | T | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(14): Show |
17 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.67+10560A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76061862 | |||||||
chr6:76062327 | G | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+10095C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062327 | |||||||
chr6:76062329 | A | C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+10093T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062329 | |||||||
chr6:76062414 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0007g0056 others(1): Show |
4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+10008A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062414 | |||||||
chr6:76062432 | C | T | 1 | a0016c0025t0001g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67+9990G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062432 | |||||||
chr6:76062443 | A | C | 20 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0187 others(17): Show |
20 | HG00621.hp1 HG02055.hp1 HG03942.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+9979T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062443 | |||||||
chr6:76062848 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.67+9574T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062848 | |||||||
chr6:76062855 | GT | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(48): Show |
52 | HG00609.hp2 HG00673.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.67+9566delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062855 | |||||||
chr6:76062855 | GTT | G | 203 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0042 others(200): Show |
204 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.67+9565_67+9566del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062855 | |||||||
chr6:76062855 | GTTT | G | 14 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0259 others(11): Show |
14 | HG01884.hp2 HG01975.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+9564_67+9566del others(3): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062855 | |||||||
chr6:76062872 | T | C | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+9550A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062872 | |||||||
chr6:76062896 | G | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0020 others(269): Show |
274 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.67+9526C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062896 | |||||||
chr6:76062915 | T | C | 2 | a0001c0001t0001g0070 a0002c0002t0001g0169 |
2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.67+9507A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062915 | |||||||
chr6:76062950 | T | C | 5 | a0001c0001t0001g0163 a0002c0002t0001g0164 a0003c0003t0002g0167 others(2): Show |
5 | NA18960.hp2 NA18979.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+9472A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062950 | |||||||
chr6:76062952 | C | T | 1 | a0002c0002t0001g0078 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.67+9470G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76062952 | |||||||
chr6:76063122 | G | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+9300C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063122 | |||||||
chr6:76063590 | G | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8832C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063590 | |||||||
chr6:76063748 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(12): Show |
15 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+8674G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063748 | |||||||
chr6:76063911 | G | A | 1 | a0009c0009t0001g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+8511C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063911 | |||||||
chr6:76063932 | G | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8490C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063932 | |||||||
chr6:76063988 | G | GT | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+8433dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76063988 | |||||||
chr6:76064060 | C | T | 9 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0247 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+8362G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064060 | |||||||
chr6:76064068 | C | G | 1 | a0008c0008t0001g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.67+8354G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064068 | |||||||
chr6:76064070 | G | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+8352C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064070 | |||||||
chr6:76064140 | A | AAGGACAG others(20): Show |
1 | a0005c0006t0003g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67+8255_67+8281dup others(27): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064140 | |||||||
chr6:76064234 | G | A | 127 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+8188C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064234 | |||||||
chr6:76064253 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67+8169C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064253 | |||||||
chr6:76064303 | G | A | 127 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+8119C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064303 | |||||||
chr6:76064360 | A | AT | 32 | a0001c0001t0001g0002 a0001c0001t0001g0259 a0001c0001t0001g0265 others(29): Show |
33 | HG00673.hp2 HG01167.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.67+8061dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064360 | |||||||
chr6:76064370 | C | T | 4 | a0001c0001t0001g0263 a0002c0002t0001g0267 a0002c0002t0001g0268 others(1): Show |
4 | HG01074.hp1 HG01993.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+8052G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064370 | |||||||
chr6:76064370 | CT | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(237): Show |
241 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.67+8051delA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064370 | |||||||
chr6:76064370 | CTT | C | 6 | a0001c0001t0001g0237 a0003c0003t0001g0179 a0004c0004t0002g0033 others(3): Show |
6 | HG01070.hp2 HG01169.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+8050_67+8051del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064370 | |||||||
chr6:76064371 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.67+8051A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064371 | |||||||
chr6:76064375 | T | C | 2 | a0002c0002t0001g0230 a0012c0012t0004g0229 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.67+8047A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064375 | |||||||
chr6:76064504 | A | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+7918T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064504 | |||||||
chr6:76064554 | A | T | 9 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0247 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+7868T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064554 | |||||||
chr6:76064691 | G | A | 1 | a0007c0007t0004g0231 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.67+7731C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064691 | |||||||
chr6:76064694 | C | T | 3 | a0002c0002t0001g0074 a0002c0002t0005g0076 a0003c0003t0001g0075 |
3 | HG02257.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.67+7728G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064694 | |||||||
chr6:76064768 | T | A | 1 | a0002c0002t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67+7654A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064768 | |||||||
chr6:76064783 | G | C | 1 | a0006c0005t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.67+7639C>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76064783 | |||||||
chr6:76065176 | A | G | 3 | a0004c0004t0002g0071 a0004c0004t0002g0072 a0004c0004t0002g0073 |
3 | HG02523.hp2 NA18947.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.67+7246T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065176 | |||||||
chr6:76065206 | T | G | 1 | a0005c0006t0003g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67+7216A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065206 | |||||||
chr6:76065251 | T | A | 1 | a0002c0002t0007g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+7171A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065251 | |||||||
chr6:76065254 | A | C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+7168T>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065254 | |||||||
chr6:76065275 | A | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
20 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+7147T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065275 | |||||||
chr6:76065424 | A | G | 2 | a0001c0001t0001g0070 a0002c0002t0001g0069 |
2 | HG02135.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.67+6998T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065424 | |||||||
chr6:76065467 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+6955G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065467 | |||||||
chr6:76065521 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+6901G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065521 | |||||||
chr6:76065544 | A | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+6878T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065544 | |||||||
chr6:76065577 | G | T | 2 | a0003c0003t0001g0066 a0003c0003t0001g0067 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.67+6845C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065577 | |||||||
chr6:76065659 | T | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+6763A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065659 | |||||||
chr6:76065705 | T | A | 1 | a0010c0010t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+6717A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76065705 | |||||||
chr6:76066419 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.67+6003G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066419 | |||||||
chr6:76066515 | C | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+5907G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066515 | |||||||
chr6:76066706 | C | T | 1 | a0002c0002t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.67+5716G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066706 | |||||||
chr6:76066780 | A | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+5642T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066780 | |||||||
chr6:76066980 | T | TA | 5 | a0001c0001t0001g0236 a0003c0003t0001g0232 a0003c0003t0001g0234 others(2): Show |
5 | NA18966.hp2 NA18970.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+5441dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76066980 | |||||||
chr6:76067013 | C | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0007c0007t0004g0058 |
3 | HG02896.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.67+5409G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067013 | |||||||
chr6:76067214 | T | TA | 9 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(6): Show |
9 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+5207dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067214 | |||||||
chr6:76067507 | T | C | 127 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+4915A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067507 | |||||||
chr6:76067633 | TA | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0237 others(2): Show |
5 | HG02896.hp1 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4788delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067633 | |||||||
chr6:76067716 | C | T | 4 | a0007c0007t0004g0241 a0007c0007t0004g0242 a0007c0007t0004g0243 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+4706G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067716 | |||||||
chr6:76067727 | C | T | 1 | a0001c0018t0001g0262 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+4695G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067727 | |||||||
chr6:76067807 | G | T | 84 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(81): Show |
85 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.67+4615C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067807 | |||||||
chr6:76067879 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.67+4543G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067879 | |||||||
chr6:76067989 | A | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4433T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76067989 | |||||||
chr6:76068181 | T | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(1): Show |
4 | NA18941.hp2 NA18974.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4241A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068181 | |||||||
chr6:76068211 | T | TA | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4210dupT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068211 | |||||||
chr6:76068322 | C | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+4100G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068322 | |||||||
chr6:76068505 | C | G | 84 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0052 others(81): Show |
85 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.67+3917G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068505 | |||||||
chr6:76068510 | C | CT | 172 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.67+3911dupA | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068510 | |||||||
chr6:76068512 | T | TTC | 27 | a0001c0001t0001g0002 a0001c0001t0001g0270 a0001c0001t0001g0271 others(24): Show |
28 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+3909_67+3910ins others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068512 | |||||||
chr6:76068591 | C | T | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3831G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068591 | |||||||
chr6:76068642 | A | G | 127 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0070 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+3780T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068642 | |||||||
chr6:76068715 | C | A | 1 | a0004c0004t0002g0240 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.67+3707G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068715 | |||||||
chr6:76068717 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(286): Show |
291 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.67+3705T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068717 | |||||||
chr6:76068731 | G | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3691C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068731 | |||||||
chr6:76068802 | C | G | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3620G>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068802 | |||||||
chr6:76068832 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+3590T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068832 | |||||||
chr6:76068903 | A | G | 1 | a0009c0009t0001g0064 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.67+3519T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76068903 | |||||||
chr6:76069226 | T | C | 1 | a0001c0026t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+3196A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069226 | |||||||
chr6:76069423 | C | T | 5 | a0001c0001t0001g0061 a0002c0002t0001g0059 a0002c0002t0001g0062 others(2): Show |
5 | HG02647.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2999G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069423 | |||||||
chr6:76069509 | A | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0007g0056 others(1): Show |
4 | HG02896.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2913T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069509 | |||||||
chr6:76069513 | C | A | 1 | a0006c0005t0001g0037 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+2909G>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069513 | |||||||
chr6:76069736 | T | C | 1 | a0002c0002t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.67+2686A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069736 | |||||||
chr6:76069745 | CA | C | 228 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0041 others(225): Show |
229 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.67+2676delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069745 | |||||||
chr6:76069745 | CAA | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(22): Show |
25 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+2675_67+2676del others(2): Show |
IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069745 | |||||||
chr6:76069895 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02027.hp2 HG02071.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2527G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069895 | |||||||
chr6:76069990 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0004c0004t0002g0036 others(1): Show |
4 | HG02074.hp1 NA18944.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2432C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76069990 | |||||||
chr6:76070218 | T | A | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0002c0002t0007g0255 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2204A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070218 | |||||||
chr6:76070320 | G | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0263 a0001c0001t0009g0260 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+2102C>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070320 | |||||||
chr6:76070370 | A | T | 7 | a0001c0001t0001g0042 a0002c0002t0001g0048 a0003c0003t0001g0043 others(4): Show |
7 | NA18953.hp1 NA18959.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2052T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070370 | |||||||
chr6:76070623 | C | T | 4 | a0001c0001t0001g0041 a0014c0014t0001g0038 a0014c0014t0001g0040 others(1): Show |
4 | NA18969.hp2 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1799G>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070623 | |||||||
chr6:76070821 | GA | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(8): Show |
11 | HG02145.hp1 HG02559.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+1600delT | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070821 | |||||||
chr6:76070873 | A | T | 2 | a0003c0003t0006g0005 a0003c0003t0006g0006 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.67+1549T>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76070873 | |||||||
chr6:76071278 | A | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
20 | HG00597.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+1144T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071278 | |||||||
chr6:76071351 | A | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0005g0010 others(12): Show |
15 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+1071T>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071351 | |||||||
chr6:76071425 | T | C | 1 | a0006c0005t0002g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.67+997A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071425 | |||||||
chr6:76071662 | T | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0265 a0001c0001t0001g0270 others(25): Show |
29 | HG00673.hp2 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.67+760A>C | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071662 | |||||||
chr6:76071746 | T | C | 3 | a0002c0002t0001g0294 a0015c0017t0001g0292 a0015c0017t0001g0293 |
3 | HG01884.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+676A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76071746 | |||||||
chr6:76072026 | T | C | 3 | a0001c0001t0001g0295 a0002c0002t0001g0296 a0002c0002t0001g0297 |
3 | NA18945.hp1 NA18987.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.67+396A>G | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072026 | |||||||
chr6:76072331 | T | A | 2 | a0001c0001t0001g0298 a0010c0010t0001g0299 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.67+91A>T | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072331 | |||||||
chr6:76072349 | G | T | 2 | a0001c0001t0001g0004 a0001c0001t0010g0003 |
2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.67+73C>A | IMPG1 | ENSG00000112706.12 | transcript | ENST00000369950.8 | protein_coding | 1/16 | chr6 | 76072349 |