Item | Value |
---|---|
geneid | 11086 |
ensemblid | ENSG00000168594.15 |
hgncid | 207 |
symbol | ADAM29 |
name | ADAM metallopeptidase domain 29 |
refseq_nuc | NM_014269.4 |
refseq_prot | NP_055084.3 |
ensembl_nuc | ENST00000359240.7 |
ensembl_prot | ENSP00000352177.3 |
mane_status | MANE Select |
chr | chr4 |
start | 174918358 |
end | 174978180 |
strand | + |
ver | v1.2 |
region | chr4:174918358-174978180 |
region5000 | chr4:174913358-174983180 |
regionname0 | ADAM29_chr4_174918358_174978180 |
regionname5000 | ADAM29_chr4_174913358_174983180 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 820 | 205 | 47 | 46 | 74 | 5 | 31 | 50 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0002 | 0/0 | 838 | 55 | 5 | 13 | 30 | 1 | 6 | 26 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(833): Show |
chr4 | 174913358 | 174983180 |
a0003 | 0/0 | 820 | 32 | 0 | 1 | 26 | 0 | 5 | 13 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0004 | 0/0 | 820 | 26 | 22 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0005 | 0/0 | 820 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0006 | 0/0 | 820 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0007 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0008 | 0/0 | 820 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0009 | 0/0 | 820 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(815): Show |
chr4 | 174913358 | 174983180 |
a0010 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | MKMLL others(736): Show |
chr4 | 174913358 | 174983180 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2460 | 197 | 39 | 46 | 74 | 5 | 31 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0001c0006 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0001c0008 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0001c0009 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0001c0013 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0001c0016 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0002c0002 | 0/0 | 2514 | 55 | 5 | 13 | 30 | 1 | 6 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2509): Show |
chr4 | 174913358 | 174983180 | ||
a0003c0003 | 0/0 | 2460 | 32 | 0 | 1 | 26 | 0 | 5 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0004c0004 | 0/0 | 2460 | 25 | 21 | 4 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0004c0015 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2509): Show |
chr4 | 174913358 | 174983180 | ||
a0005c0005 | 0/0 | 2514 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2509): Show |
chr4 | 174913358 | 174983180 | ||
a0005c0007 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0006c0010 | 0/0 | 2460 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0007c0011 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0008c0014 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0009c0012 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 | ||
a0010c0017 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | ATGAA others(2455): Show |
chr4 | 174913358 | 174983180 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3327 | 96 | 10 | 17 | 59 | 2 | 8 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0002 | 0/0 | 3327 | 43 | 16 | 9 | 10 | 0 | 8 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0003 | 0/1 | 3327 | 33 | 3 | 14 | 1 | 3 | 11 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0004 | 1/0 | 3325 | 12 | 3 | 6 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3320): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0005 | 0/0 | 3325 | 5 | 3 | 0 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3320): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0006 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0007 | 0/0 | 3327 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0008 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0001t0015 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0006t0002 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0008t0002 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0009t0011 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3320): Show |
chr4 | 174913358 | 174983180 |
a0001c0009t0013 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0013t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0001c0016t0002 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0002c0002t0001 | 0/0 | 3381 | 28 | 2 | 7 | 17 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3376): Show |
chr4 | 174913358 | 174983180 |
a0002c0002t0002 | 0/0 | 3381 | 6 | 2 | 0 | 1 | 0 | 3 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3376): Show |
chr4 | 174913358 | 174983180 |
a0002c0002t0003 | 0/0 | 3381 | 5 | 0 | 4 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3376): Show |
chr4 | 174913358 | 174983180 |
a0002c0002t0004 | 0/0 | 3379 | 15 | 1 | 1 | 11 | 1 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3374): Show |
chr4 | 174913358 | 174983180 |
a0002c0002t0012 | 0/0 | 3381 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3376): Show |
chr4 | 174913358 | 174983180 |
a0003c0003t0001 | 0/0 | 3327 | 8 | 0 | 1 | 6 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0003c0003t0002 | 0/0 | 3327 | 24 | 0 | 0 | 20 | 0 | 4 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0004c0004t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0004c0004t0002 | 0/0 | 3327 | 19 | 15 | 4 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0004c0004t0004 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3320): Show |
chr4 | 174913358 | 174983180 |
a0004c0004t0006 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0004c0004t0009 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0004c0004t0010 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0004c0015t0002 | 0/0 | 3381 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3376): Show |
chr4 | 174913358 | 174983180 |
a0005c0005t0002 | 0/0 | 3381 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3376): Show |
chr4 | 174913358 | 174983180 |
a0005c0007t0002 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0006c0010t0003 | 0/0 | 3327 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0007c0011t0002 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0008c0014t0001 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0009c0012t0014 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
a0010c0017t0002 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | GTGAC others(3322): Show |
chr4 | 174913358 | 174983180 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0001t0015g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0006t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0006t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0008t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0008t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0009t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0009t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0013t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0001c0016t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0007 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0002c0002t0012g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0003c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0004t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0004c0015t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0005t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0005t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0005t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0007t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0005c0007t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0006c0010t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0006c0010t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0007c0011t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0008c0014t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0009c0012t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
a0010c0017t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0062 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00408 | hp2 | a0003 | c0003 | t0002 | g0254 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00438 | hp2 | a0003 | c0003 | t0002 | g0025 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00544 | hp1 | a0002 | c0002 | t0004 | g0095 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00621 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00639 | hp1 | a0004 | c0004 | t0002 | g0269 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00639 | hp2 | a0006 | c0010 | t0003 | g0057 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00642 | hp2 | a0002 | c0002 | t0012 | g0050 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00735 | hp2 | a0002 | c0002 | t0003 | g0044 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0091 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00741 | hp1 | a0004 | c0004 | t0002 | g0267 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01106 | hp1 | a0002 | c0002 | t0003 | g0074 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01109 | hp1 | a0004 | c0004 | t0002 | g0027 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0075 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01433 | hp1 | a0004 | c0004 | t0002 | g0262 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01891 | hp1 | a0001 | c0008 | t0002 | g0100 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0214 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01981 | hp1 | a0006 | c0010 | t0003 | g0067 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02040 | hp1 | a0002 | c0002 | t0004 | g0092 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02056 | hp1 | a0003 | c0003 | t0002 | g0243 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02071 | hp2 | a0002 | c0002 | t0004 | g0098 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02074 | hp1 | a0007 | c0011 | t0002 | g0245 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02129 | hp1 | a0003 | c0003 | t0002 | g0183 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02135 | hp1 | a0003 | c0003 | t0002 | g0232 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02155 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CDX | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0132 | EAS | CDX | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02258 | hp2 | a0004 | c0004 | t0009 | g0233 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0061 | AMR | PEL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02451 | hp1 | a0004 | c0004 | t0002 | g0272 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02572 | hp1 | a0004 | c0004 | t0002 | g0036 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02602 | hp1 | a0003 | c0003 | t0002 | g0005 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0081 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02615 | hp1 | a0004 | c0004 | t0002 | g0235 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02622 | hp1 | a0001 | c0008 | t0002 | g0099 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02630 | hp1 | a0001 | c0013 | t0001 | g0187 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02630 | hp2 | a0005 | c0007 | t0002 | g0222 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02647 | hp2 | a0004 | c0004 | t0002 | g0028 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02723 | hp2 | a0004 | c0004 | t0009 | g0234 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02809 | hp1 | a0005 | c0007 | t0002 | g0224 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02818 | hp1 | a0001 | c0016 | t0002 | g0039 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02818 | hp2 | a0008 | c0014 | t0001 | g0137 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02886 | hp1 | a0005 | c0005 | t0002 | g0223 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02886 | hp2 | a0004 | c0004 | t0010 | g0176 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02895 | hp1 | a0005 | c0005 | t0002 | g0024 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02895 | hp2 | a0004 | c0004 | t0002 | g0260 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02897 | hp1 | a0005 | c0005 | t0002 | g0024 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02922 | hp1 | a0001 | c0009 | t0013 | g0041 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03041 | hp2 | a0004 | c0004 | t0002 | g0261 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03098 | hp1 | a0001 | c0009 | t0011 | g0097 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03098 | hp2 | a0004 | c0004 | t0006 | g0054 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03139 | hp1 | a0004 | c0004 | t0002 | g0174 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03209 | hp2 | a0004 | c0004 | t0001 | g0202 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03225 | hp2 | a0001 | c0006 | t0002 | g0033 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0178 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03453 | hp2 | a0004 | c0004 | t0004 | g0078 | AFR | MSL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0230 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03516 | hp1 | a0004 | c0004 | t0002 | g0029 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0082 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03704 | hp1 | a0003 | c0003 | t0002 | g0229 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0179 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03927 | hp2 | a0003 | c0003 | t0002 | g0274 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0158 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04199 | hp2 | a0003 | c0003 | t0002 | g0241 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | STU | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18522 | hp1 | a0004 | c0004 | t0002 | g0029 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18612 | hp1 | a0003 | c0003 | t0002 | g0135 | EAS | CHB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18906 | hp2 | a0004 | c0004 | t0002 | g0027 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0251 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18944 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18945 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18950 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18957 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18972 | hp2 | a0001 | c0001 | t0015 | g0116 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18973 | hp2 | a0010 | c0017 | t0002 | g0275 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18981 | hp1 | a0003 | c0003 | t0002 | g0258 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18981 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0087 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0196 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18986 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18989 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18992 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19043 | hp2 | a0005 | c0005 | t0002 | g0225 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19065 | hp2 | a0003 | c0003 | t0002 | g0256 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19074 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19080 | hp1 | a0002 | c0002 | t0004 | g0093 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19080 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19083 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19091 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0088 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA19240 | hp2 | a0004 | c0015 | t0002 | g0227 | AFR | YRI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20129 | hp1 | a0004 | c0004 | t0002 | g0228 | AFR | ASW | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0263 | AFR | ASW | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20752 | hp1 | a0002 | c0002 | t0004 | g0083 | EUR | TSI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0046 | EUR | TSI | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | GIH | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | GIH | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01123 | hp1 | a0002 | c0002 | t0004 | g0079 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02109 | hp1 | a0004 | c0004 | t0002 | g0264 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02486 | hp1 | a0004 | c0004 | t0002 | g0266 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02559 | hp1 | a0004 | c0004 | t0002 | g0028 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG06807 | hp1 | a0009 | c0012 | t0014 | g0034 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA20300 | hp2 | a0001 | c0006 | t0002 | g0035 | AFR | USA | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | LWK | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0049 | REF | REF | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0084 | REF | REF | ADAM29_chr4_174913358_174983180 | ADAM29 | chr4 | 174913358 | 174983180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174976088 | G | C | 1 | a0007 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.563G>C | p.Ser188Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 1233/3325 | 563/2463 | 188/820 | chr4 | 174976088 | |||
chr4:174977404 | C | T | 3 | a0003 a0007 a0010 |
34 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(31): Show |
missense_variant | MODERATE | c.1879C>T | p.Pro627Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2549/3325 | 1879/2463 | 627/820 | chr4 | 174977404 | |||
chr4:174977693 | G | A | 1 | a0009 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.2168G>A | p.Arg723His | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2838/3325 | 2168/2463 | 723/820 | chr4 | 174977693 | |||
chr4:174977749 | C | T | 1 | a0010 | 1 | NA18973.hp2 | stop_gained | HIGH | c.2224C>T | p.Gln742* | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2894/3325 | 2224/2463 | 742/820 | chr4 | 174977749 | |||
chr4:174977783 | A | G | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2258A>G | p.Gln753Arg | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2928/3325 | 2258/2463 | 753/820 | chr4 | 174977783 | |||
chr4:174977816 | C | T | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2291C>T | p.Thr764Ile | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2961/3325 | 2291/2463 | 764/820 | chr4 | 174977816 | |||
chr4:174977832 | A | T | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2307A>T | p.Gln769His | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2977/3325 | 2307/2463 | 769/820 | chr4 | 174977832 | |||
chr4:174977837 | G | A | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2312G>A | p.Arg771Gln | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2982/3325 | 2312/2463 | 771/820 | chr4 | 174977837 | |||
chr4:174977839 | G | T | 1 | a0006 | 2 | HG00639.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.2314G>T | p.Val772Leu | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2984/3325 | 2314/2463 | 772/820 | chr4 | 174977839 | |||
chr4:174977843 | T | C | 2 | a0006 a0008 |
3 | HG00639.hp2 HG01981.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.2318T>C | p.Met773Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2988/3325 | 2318/2463 | 773/820 | chr4 | 174977843 | |||
chr4:174977850 | T | TCAGAGTC others(47): Show |
1 | a0002 | 55 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(52): Show |
disruptive_inframe_insertion | MODERATE | c.2345_2398dupTGCCTT others(48): Show |
p.Met782_Val799dup | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3069/3325 | 2399/2463 | 800/820 | INFO_REALIGN_3_PRIME | chr4 | 174977850 | ||
chr4:174977870 | T | C | 1 | a0004 | 26 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(23): Show |
missense_variant | MODERATE | c.2345T>C | p.Met782Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3015/3325 | 2345/2463 | 782/820 | chr4 | 174977870 | |||
chr4:174977937 | G | GCAACCTC others(47): Show |
1 | a0005 | 4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
stop_gained&conservative_inframe_insertion | HIGH | c.2436_2437insGGTCAA others(48): Show |
p.Gln812_Ser813insGl others(52): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3107/3325 | 2437/2463 | 813/820 | INFO_REALIGN_3_PRIME | chr4 | 174977937 | ||
chr4:174977962 | A | G | 1 | a0005 | 2 | HG02630.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.2437A>G | p.Ser813Gly | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3107/3325 | 2437/2463 | 813/820 | chr4 | 174977962 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174976095 | T | C | 4 | a0001c0006 a0005c0005 a0005c0007 others(1): Show |
9 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(6): Show |
synonymous_variant | LOW | c.570T>C | p.Tyr190Tyr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 1240/3325 | 570/2463 | 190/820 | chr4 | 174976095 | |||
chr4:174976359 | G | A | 1 | a0001c0013 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.834G>A | p.Thr278Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 1504/3325 | 834/2463 | 278/820 | chr4 | 174976359 | |||
chr4:174977559 | T | C | 1 | a0001c0008 | 2 | HG01891.hp1 HG02622.hp1 |
synonymous_variant | LOW | c.2034T>C | p.Tyr678Tyr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2704/3325 | 2034/2463 | 678/820 | chr4 | 174977559 | |||
chr4:174977763 | G | A | 1 | a0001c0009 | 2 | HG02922.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.2238G>A | p.Thr746Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2908/3325 | 2238/2463 | 746/820 | chr4 | 174977763 | |||
chr4:174977796 | C | T | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2271C>T | p.Ser757Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2941/3325 | 2271/2463 | 757/820 | chr4 | 174977796 | |||
chr4:174977817 | A | G | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2292A>G | p.Thr764Thr | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2962/3325 | 2292/2463 | 764/820 | chr4 | 174977817 | |||
chr4:174977820 | C | T | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2295C>T | p.Pro765Pro | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2965/3325 | 2295/2463 | 765/820 | chr4 | 174977820 | |||
chr4:174977850 | T | C | 1 | a0006c0010 | 2 | HG00639.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.2325T>C | p.Ser775Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 2995/3325 | 2325/2463 | 775/820 | chr4 | 174977850 | |||
chr4:174977877 | C | A | 1 | a0001c0016 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2352C>A | p.Ser784Ser | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 3022/3325 | 2352/2463 | 784/820 | chr4 | 174977877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174918369 | T | C | 1 | a0004c0004t0010 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-659T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/5 | 57157 | chr4 | 174918369 | ||||||
chr4:174918404 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(23): Show |
257 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-624A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/5 | chr4 | 174918404 | |||||||
chr4:174918460 | G | A | 1 | a0001c0001t0008 | 2 | HG03130.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-568G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/5 | 57066 | chr4 | 174918460 | ||||||
chr4:174920749 | G | T | 4 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0012 others(1): Show |
40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-494G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/5 | 54777 | chr4 | 174920749 | ||||||
chr4:174931001 | A | ATG | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
5_prime_UTR_variant | MODIFIER | c.-434_-433insGT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/5 | 44523 | INFO_REALIGN_3_PRIME | chr4 | 174931001 | |||||
chr4:174931004 | C | T | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0015 others(6): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-432C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/5 | 44522 | chr4 | 174931004 | ||||||
chr4:174931027 | G | A | 1 | a0004c0004t0009 | 2 | HG02258.hp2 HG02723.hp2 |
5_prime_UTR_variant | MODIFIER | c.-409G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/5 | 44499 | chr4 | 174931027 | ||||||
chr4:174975361 | G | A | 1 | a0001c0001t0007 | 3 | HG00609.hp1 NA19010.hp1 NA19090.hp1 |
5_prime_UTR_variant | MODIFIER | c.-165G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 165 | chr4 | 174975361 | ||||||
chr4:174975456 | A | T | 1 | a0001c0009t0011 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 70 | chr4 | 174975456 | ||||||
chr4:174977937 | G | GCAACCTC others(47): Show |
1 | a0004c0015t0002 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.2461_*51dupTAGAGCC others(47): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 52 | INFO_REALIGN_3_PRIME | chr4 | 174977937 | |||||
chr4:174978016 | A | G | 1 | a0009c0012t0014 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 28 | chr4 | 174978016 | ||||||
chr4:174978094 | C | T | 1 | a0001c0001t0015 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 106 | chr4 | 174978094 | ||||||
chr4:174978122 | C | T | 2 | a0001c0009t0011 a0001c0009t0013 |
2 | HG02922.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*134C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 5/5 | 134 | chr4 | 174978122 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:174918574 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(67): Show |
88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-557+103C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918574 | |||||||
chr4:174918576 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(78): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-557+105G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918576 | |||||||
chr4:174918585 | G | T | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
150 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-557+114G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918585 | |||||||
chr4:174918741 | T | C | 7 | a0001c0001t0002g0037 a0001c0006t0002g0033 a0001c0006t0002g0035 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-557+270T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918741 | |||||||
chr4:174918747 | T | TA | 12 | a0001c0001t0003g0012 a0001c0001t0003g0042 a0001c0001t0003g0043 others(9): Show |
13 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.-557+284dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 174918747 | ||||||
chr4:174918812 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-557+341A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918812 | |||||||
chr4:174918895 | T | C | 5 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0002c0002t0002g0031 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-557+424T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918895 | |||||||
chr4:174918952 | A | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
257 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-557+481A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174918952 | |||||||
chr4:174919271 | A | G | 1 | a0001c0001t0002g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-557+800A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919271 | |||||||
chr4:174919586 | T | C | 9 | a0001c0001t0002g0221 a0001c0001t0002g0226 a0004c0004t0002g0228 others(6): Show |
10 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-556-1101T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919586 | |||||||
chr4:174919633 | C | G | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-556-1054C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919633 | |||||||
chr4:174919741 | T | C | 1 | a0003c0003t0002g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-556-946T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919741 | |||||||
chr4:174919751 | G | A | 257 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.-556-936G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919751 | |||||||
chr4:174919752 | T | C | 61 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(58): Show |
78 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-556-935T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174919752 | |||||||
chr4:174920007 | T | A | 1 | a0002c0002t0001g0103 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-556-680T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920007 | |||||||
chr4:174920033 | T | C | 8 | a0001c0001t0003g0012 a0001c0001t0003g0042 a0001c0001t0003g0043 others(5): Show |
9 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-556-654T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920033 | |||||||
chr4:174920083 | G | A | 7 | a0001c0001t0002g0037 a0001c0006t0002g0033 a0001c0006t0002g0035 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-556-604G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920083 | |||||||
chr4:174920113 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-556-574A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920113 | |||||||
chr4:174920150 | C | G | 3 | a0001c0001t0004g0014 a0001c0001t0006g0077 a0004c0004t0004g0078 |
4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-556-537C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920150 | |||||||
chr4:174920164 | C | T | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-556-523C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920164 | |||||||
chr4:174920185 | A | T | 1 | a0002c0002t0004g0098 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-556-502A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920185 | |||||||
chr4:174920498 | C | T | 1 | a0001c0001t0003g0006 | 3 | HG01106.hp2 HG01123.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-556-189C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920498 | |||||||
chr4:174920550 | G | T | 1 | a0001c0001t0002g0277 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-556-137G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | chr4 | 174920550 | |||||||
chr4:174920962 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
18 | HG00323.hp2 HG01192.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-451+170A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174920962 | |||||||
chr4:174921011 | A | G | 3 | a0001c0001t0002g0276 a0001c0001t0008g0101 a0001c0001t0008g0102 |
3 | HG01070.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+219A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921011 | |||||||
chr4:174921079 | A | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
163 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-451+287A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921079 | |||||||
chr4:174921343 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-451+551C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921343 | |||||||
chr4:174921344 | G | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(71): Show |
92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-451+552G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921344 | |||||||
chr4:174921429 | T | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
255 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-451+637T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921429 | |||||||
chr4:174921478 | C | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02132.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-451+686C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921478 | |||||||
chr4:174921504 | A | G | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+712A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921504 | |||||||
chr4:174921580 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-451+788G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921580 | |||||||
chr4:174921635 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
255 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-451+843A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921635 | |||||||
chr4:174921828 | G | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(71): Show |
92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-451+1036G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921828 | |||||||
chr4:174921832 | G | A | 2 | a0001c0001t0002g0231 a0002c0002t0002g0230 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-451+1040G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921832 | |||||||
chr4:174921891 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0231 a0001c0008t0002g0099 others(2): Show |
8 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-451+1099G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174921891 | |||||||
chr4:174922016 | A | G | 1 | a0010c0017t0002g0275 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-451+1224A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922016 | |||||||
chr4:174922077 | A | G | 3 | a0001c0001t0004g0014 a0001c0001t0006g0077 a0004c0004t0004g0078 |
4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-451+1285A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922077 | |||||||
chr4:174922174 | C | T | 5 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0002c0002t0002g0031 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-451+1382C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922174 | |||||||
chr4:174922223 | AT | A | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+1432delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922223 | |||||||
chr4:174922226 | C | A | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+1434C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922226 | |||||||
chr4:174922277 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-451+1485A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922277 | |||||||
chr4:174922306 | G | A | 2 | a0001c0001t0002g0037 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+1514G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922306 | |||||||
chr4:174922455 | C | G | 1 | a0003c0003t0002g0274 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-451+1663C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922455 | |||||||
chr4:174922729 | TA | T | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+1943delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174922729 | ||||||
chr4:174922744 | C | T | 2 | a0001c0001t0002g0037 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+1952C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922744 | |||||||
chr4:174922778 | T | C | 1 | a0003c0003t0002g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-451+1986T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174922778 | |||||||
chr4:174923009 | G | A | 9 | a0001c0001t0002g0221 a0001c0001t0002g0226 a0004c0004t0002g0228 others(6): Show |
10 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-451+2217G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923009 | |||||||
chr4:174923065 | TA | T | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(78): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2274delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923065 | |||||||
chr4:174923119 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(78): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2327G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923119 | |||||||
chr4:174923156 | G | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(253): Show |
301 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.-451+2364G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923156 | |||||||
chr4:174923205 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-451+2413C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923205 | |||||||
chr4:174923214 | A | G | 2 | a0001c0001t0002g0273 a0001c0001t0002g0278 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-451+2422A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923214 | |||||||
chr4:174923245 | C | G | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+2453C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923245 | |||||||
chr4:174923306 | C | T | 1 | a0001c0009t0011g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-451+2514C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923306 | |||||||
chr4:174923350 | T | C | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+2558T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923350 | |||||||
chr4:174923380 | T | G | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(78): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2588T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923380 | |||||||
chr4:174923434 | G | C | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(78): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+2642G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923434 | |||||||
chr4:174923519 | T | TGATA | 8 | a0001c0001t0002g0226 a0004c0004t0002g0028 a0004c0004t0002g0261 others(5): Show |
9 | HG01433.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-451+2727_-451+272 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923519 | |||||||
chr4:174923519 | T | TGATATA | 8 | a0001c0001t0002g0221 a0001c0009t0013g0041 a0004c0004t0002g0027 others(5): Show |
10 | HG01109.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-451+2727_-451+272 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923519 | |||||||
chr4:174923519 | TTATATGT others(1): Show |
T | 6 | a0001c0001t0002g0257 a0002c0002t0002g0255 a0002c0002t0002g0259 others(3): Show |
6 | HG02559.hp2 HG03239.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-451+2733_-451+274 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | ||||||
chr4:174923519 | TTATATGT others(3): Show |
T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(31): Show |
47 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.-451+2733_-451+274 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | ||||||
chr4:174923519 | TTATATGT others(9): Show |
T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0016t0002g0039 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+2733_-451+274 others(20): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | ||||||
chr4:174923519 | TTATATGT others(17): Show |
T | 3 | a0001c0006t0002g0035 a0004c0004t0009g0233 a0004c0004t0009g0234 |
3 | HG02258.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-451+2733_-451+275 others(28): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923519 | ||||||
chr4:174923520 | T | G | 9 | a0001c0001t0002g0268 a0001c0001t0002g0278 a0004c0004t0002g0029 others(6): Show |
10 | HG00639.hp1 HG00741.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-451+2728T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923520 | |||||||
chr4:174923523 | ATG | A | 4 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0004c0004t0002g0228 others(1): Show |
4 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-451+2733_-451+273 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923523 | ||||||
chr4:174923525 | G | A | 28 | a0001c0001t0002g0037 a0001c0001t0002g0221 a0001c0001t0002g0226 others(25): Show |
32 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.-451+2733G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923525 | |||||||
chr4:174923525 | G | GTGTA | 9 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0151 others(6): Show |
12 | HG00609.hp2 HG00673.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTATA | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
53 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTATAT others(1): Show |
26 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0001g0111 others(23): Show |
26 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTATAT others(3): Show |
17 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0001g0152 others(14): Show |
17 | HG00408.hp1 HG00438.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTATAT others(5): Show |
28 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0017 others(25): Show |
33 | HG00323.hp2 HG01168.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTATAT others(7): Show |
8 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0184 others(5): Show |
9 | HG00558.hp2 HG01261.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.-451+2734_-451+273 others(18): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTATAT others(13): Show |
1 | a0002c0002t0001g0133 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-451+2734_-451+273 others(24): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | G | GTGTGTGT others(3): Show |
1 | a0002c0002t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-451+2734_-451+273 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | GTA | G | 7 | a0001c0001t0004g0015 a0001c0001t0004g0085 a0001c0001t0006g0096 others(4): Show |
7 | HG00544.hp1 HG01168.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-451+2768_-451+276 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | GTATA | G | 4 | a0001c0001t0003g0071 a0001c0001t0004g0015 a0002c0002t0003g0075 others(1): Show |
4 | HG01256.hp2 HG01361.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-451+2766_-451+276 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | GTATATA | G | 10 | a0001c0001t0003g0013 a0001c0001t0003g0056 a0001c0001t0003g0062 others(7): Show |
12 | HG00323.hp1 HG01106.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-451+2764_-451+276 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | GTATATAT others(1): Show |
G | 25 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0042 others(22): Show |
28 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-451+2762_-451+276 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | GTATATAT others(3): Show |
G | 3 | a0001c0001t0003g0043 a0001c0001t0006g0077 a0004c0004t0006g0054 |
3 | HG01433.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-451+2760_-451+276 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923525 | GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0203 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-451+2748_-451+276 others(26): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174923525 | ||||||
chr4:174923526 | T | G | 1 | a0001c0001t0002g0030 | 2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-451+2734T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923526 | |||||||
chr4:174923528 | T | G | 6 | a0001c0001t0002g0257 a0002c0002t0002g0255 a0002c0002t0002g0259 others(3): Show |
6 | HG02559.hp2 HG03239.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-451+2736T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923528 | |||||||
chr4:174923530 | T | G | 33 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(30): Show |
46 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-451+2738T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923530 | |||||||
chr4:174923533 | A | G | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+2741A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923533 | |||||||
chr4:174923536 | T | G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0016t0002g0039 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+2744T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923536 | |||||||
chr4:174923544 | T | G | 2 | a0004c0004t0009g0233 a0004c0004t0009g0234 |
2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-451+2752T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923544 | |||||||
chr4:174923549 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-451+2757A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923549 | |||||||
chr4:174923560 | T | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(211): Show |
254 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-451+2768T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923560 | |||||||
chr4:174923602 | A | C | 2 | a0001c0001t0002g0037 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+2810A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923602 | |||||||
chr4:174923602 | A | G | 1 | a0004c0004t0001g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-451+2810A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923602 | |||||||
chr4:174923721 | A | G | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(37): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-451+2929A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923721 | |||||||
chr4:174923812 | C | A | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+3020C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923812 | |||||||
chr4:174923865 | A | C | 5 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0002c0002t0002g0031 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-451+3073A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923865 | |||||||
chr4:174923876 | C | G | 3 | a0002c0002t0001g0020 a0002c0002t0001g0200 a0002c0002t0001g0201 |
4 | NA18947.hp2 NA18962.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+3084C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923876 | |||||||
chr4:174923909 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
10 | NA18939.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.-451+3117C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923909 | |||||||
chr4:174923980 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-451+3188T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174923980 | |||||||
chr4:174924114 | T | G | 1 | a0001c0001t0002g0038 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-451+3322T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924114 | |||||||
chr4:174924283 | T | C | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+3491T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924283 | |||||||
chr4:174924440 | C | T | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+3648C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924440 | |||||||
chr4:174924596 | G | A | 1 | a0002c0002t0004g0079 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-451+3804G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924596 | |||||||
chr4:174924718 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(67): Show |
88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-451+3926C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924718 | |||||||
chr4:174924841 | G | A | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-451+4049G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924841 | |||||||
chr4:174924959 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(78): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-451+4167G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174924959 | |||||||
chr4:174925169 | A | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(73): Show |
94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-451+4377A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925169 | |||||||
chr4:174925176 | G | A | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-451+4384G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925176 | |||||||
chr4:174925204 | C | T | 1 | a0004c0004t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-451+4412C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925204 | |||||||
chr4:174925275 | C | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(67): Show |
88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-451+4483C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925275 | |||||||
chr4:174925327 | A | G | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-451+4535A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925327 | |||||||
chr4:174925349 | ACT | A | 36 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(33): Show |
40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-451+4560_-451+456 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174925349 | ||||||
chr4:174925367 | AT | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(143): Show |
169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-451+4585delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174925367 | ||||||
chr4:174925390 | A | G | 2 | a0001c0001t0002g0037 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-451+4598A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925390 | |||||||
chr4:174925405 | A | G | 1 | a0001c0006t0002g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-451+4613A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925405 | |||||||
chr4:174925456 | T | A | 1 | a0002c0002t0004g0080 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-451+4664T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925456 | |||||||
chr4:174925485 | T | C | 1 | a0004c0015t0002g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-451+4693T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925485 | |||||||
chr4:174925498 | A | G | 1 | a0002c0002t0002g0259 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-451+4706A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925498 | |||||||
chr4:174925539 | C | A | 1 | a0001c0001t0004g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-451+4747C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925539 | |||||||
chr4:174925590 | C | T | 1 | a0003c0003t0002g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-451+4798C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925590 | |||||||
chr4:174925682 | CAGG | C | 5 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0002c0002t0002g0031 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-451+4893_-451+489 others(7): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174925682 | ||||||
chr4:174925685 | G | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0009t0013g0041 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-451+4893G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925685 | |||||||
chr4:174925763 | G | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0191 others(5): Show |
11 | HG00423.hp1 HG00673.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-451+4971G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925763 | |||||||
chr4:174925825 | G | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
150 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-451+5033G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925825 | |||||||
chr4:174925993 | A | T | 74 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(71): Show |
92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-450-4993A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174925993 | |||||||
chr4:174926033 | A | G | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-450-4953A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926033 | |||||||
chr4:174926037 | A | T | 2 | a0001c0001t0006g0096 a0001c0009t0011g0097 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-450-4949A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926037 | |||||||
chr4:174926252 | C | T | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-450-4734C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926252 | |||||||
chr4:174926263 | C | T | 3 | a0001c0001t0004g0014 a0001c0001t0006g0077 a0004c0004t0004g0078 |
4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-450-4723C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926263 | |||||||
chr4:174926265 | C | T | 9 | a0001c0001t0002g0221 a0001c0001t0002g0226 a0004c0004t0002g0228 others(6): Show |
10 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-450-4721C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926265 | |||||||
chr4:174926270 | A | G | 4 | a0004c0004t0002g0028 a0004c0004t0002g0235 a0004c0004t0002g0263 others(1): Show |
5 | HG02109.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-450-4716A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926270 | |||||||
chr4:174926285 | C | A | 42 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(39): Show |
47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-450-4701C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926285 | |||||||
chr4:174926313 | A | G | 2 | a0001c0001t0002g0037 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-450-4673A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926313 | |||||||
chr4:174926376 | T | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(67): Show |
88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-450-4610T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926376 | |||||||
chr4:174926409 | T | C | 2 | a0001c0001t0001g0104 a0002c0002t0001g0105 |
2 | NA18962.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-450-4577T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926409 | |||||||
chr4:174926417 | T | G | 1 | a0004c0004t0006g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-450-4569T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926417 | |||||||
chr4:174926541 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0199 |
3 | NA18945.hp1 NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-450-4445A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926541 | |||||||
chr4:174926600 | T | C | 254 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(251): Show |
296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-450-4386T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926600 | |||||||
chr4:174926639 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-450-4347G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926639 | |||||||
chr4:174926721 | C | CA | 17 | a0001c0001t0001g0109 a0001c0001t0001g0191 a0001c0001t0001g0211 others(14): Show |
18 | HG01074.hp1 HG01934.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-450-4248dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | ||||||
chr4:174926721 | C | CAA | 6 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0009t0013g0041 others(3): Show |
6 | HG02451.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-450-4249_-450-424 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | ||||||
chr4:174926721 | C | CAAA | 58 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(55): Show |
75 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-450-4250_-450-424 others(7): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | ||||||
chr4:174926721 | CA | C | 9 | a0001c0001t0001g0190 a0001c0006t0002g0033 a0001c0006t0002g0035 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-450-4248delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174926721 | ||||||
chr4:174926758 | A | G | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(37): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-450-4228A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926758 | |||||||
chr4:174926833 | G | T | 1 | a0001c0001t0006g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-450-4153G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926833 | |||||||
chr4:174926977 | C | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-450-4009C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174926977 | |||||||
chr4:174927217 | A | C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(73): Show |
94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-450-3769A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927217 | |||||||
chr4:174927391 | A | G | 42 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(39): Show |
47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-450-3595A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927391 | |||||||
chr4:174927432 | A | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-450-3554A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927432 | |||||||
chr4:174927654 | C | A | 3 | a0001c0001t0004g0014 a0001c0001t0006g0077 a0004c0004t0004g0078 |
4 | HG03041.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-450-3332C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927654 | |||||||
chr4:174927684 | G | C | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-450-3302G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927684 | |||||||
chr4:174927887 | T | C | 1 | a0006c0010t0003g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-450-3099T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927887 | |||||||
chr4:174927936 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-450-3050T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927936 | |||||||
chr4:174927992 | C | T | 2 | a0001c0001t0002g0037 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-450-2994C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174927992 | |||||||
chr4:174928138 | A | G | 1 | a0001c0001t0006g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-450-2848A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928138 | |||||||
chr4:174928195 | A | G | 257 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.-450-2791A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928195 | |||||||
chr4:174928292 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-450-2694G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928292 | |||||||
chr4:174928292 | G | T | 40 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(37): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-450-2694G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928292 | |||||||
chr4:174928296 | G | C | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-450-2690G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928296 | |||||||
chr4:174928365 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-450-2621G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928365 | |||||||
chr4:174928569 | T | TAAAAAAA others(1): Show |
20 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0189 others(17): Show |
21 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-450-2412_-450-240 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174928569 | ||||||
chr4:174928569 | T | TAAAAAAA others(2): Show |
156 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-450-2413_-450-240 others(13): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174928569 | ||||||
chr4:174928569 | T | TAAAAAAA others(3): Show |
5 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0008g0101 others(2): Show |
5 | HG00621.hp1 HG03130.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-450-2414_-450-240 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174928569 | ||||||
chr4:174928569 | T | TTAAAA | 14 | a0001c0001t0002g0030 a0001c0001t0002g0038 a0001c0001t0002g0040 others(11): Show |
16 | HG00735.hp1 HG01243.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.-450-2417_-450-241 others(9): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928569 | |||||||
chr4:174928569 | T | TTAAAAA | 62 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(59): Show |
78 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-450-2417_-450-241 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928569 | |||||||
chr4:174928747 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-450-2239A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928747 | |||||||
chr4:174928767 | G | T | 1 | a0001c0001t0003g0076 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-450-2219G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928767 | |||||||
chr4:174928820 | A | G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0009t0013g0041 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-450-2166A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928820 | |||||||
chr4:174928833 | T | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(73): Show |
94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-450-2153T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928833 | |||||||
chr4:174928931 | G | T | 1 | a0001c0001t0001g0195 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-450-2055G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174928931 | |||||||
chr4:174929035 | A | C | 2 | a0001c0001t0005g0270 a0001c0001t0005g0271 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-450-1951A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929035 | |||||||
chr4:174929081 | G | A | 1 | a0001c0001t0006g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-450-1905G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929081 | |||||||
chr4:174929332 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-450-1654G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929332 | |||||||
chr4:174929454 | T | G | 73 | a0001c0001t0001g0119 a0001c0001t0002g0001 a0001c0001t0002g0011 others(70): Show |
91 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-450-1532T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929454 | |||||||
chr4:174929455 | T | C | 2 | a0004c0015t0002g0227 a0009c0012t0014g0034 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-450-1531T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929455 | |||||||
chr4:174929647 | GT | G | 37 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(34): Show |
41 | HG00280.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.-450-1334delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174929647 | ||||||
chr4:174929723 | T | C | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG01099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-450-1263T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929723 | |||||||
chr4:174929755 | CT | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(211): Show |
254 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.-450-1217delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 174929755 | ||||||
chr4:174929859 | C | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0040 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-450-1127C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929859 | |||||||
chr4:174929868 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-450-1118T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929868 | |||||||
chr4:174929902 | G | A | 2 | a0002c0002t0002g0255 a0002c0002t0002g0259 |
2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-450-1084G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929902 | |||||||
chr4:174929975 | C | A | 101 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(98): Show |
122 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-450-1011C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929975 | |||||||
chr4:174929984 | A | T | 1 | a0001c0001t0002g0252 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-450-1002A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929984 | |||||||
chr4:174929991 | T | C | 101 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(98): Show |
122 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-450-995T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174929991 | |||||||
chr4:174930051 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-450-935C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930051 | |||||||
chr4:174930073 | C | T | 2 | a0002c0002t0003g0074 a0002c0002t0003g0075 |
2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-450-913C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930073 | |||||||
chr4:174930369 | T | G | 67 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(64): Show |
84 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-450-617T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930369 | |||||||
chr4:174930658 | G | A | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-450-328G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930658 | |||||||
chr4:174930803 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-450-183A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930803 | |||||||
chr4:174930828 | T | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.-450-158T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | chr4 | 174930828 | |||||||
chr4:174931291 | A | T | 2 | a0001c0001t0002g0277 a0003c0003t0002g0251 |
2 | NA18942.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-262+117A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931291 | |||||||
chr4:174931337 | A | G | 9 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(6): Show |
12 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-262+163A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931337 | |||||||
chr4:174931470 | T | C | 1 | a0009c0012t0014g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-262+296T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931470 | |||||||
chr4:174931541 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-262+367T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931541 | |||||||
chr4:174931749 | T | C | 68 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(65): Show |
85 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-262+575T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931749 | |||||||
chr4:174931778 | G | T | 67 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(64): Show |
84 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-262+604G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931778 | |||||||
chr4:174931785 | C | G | 8 | a0001c0001t0002g0226 a0001c0001t0006g0096 a0004c0004t0002g0228 others(5): Show |
9 | HG02109.hp2 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-262+611C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931785 | |||||||
chr4:174931816 | T | TCA | 13 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
18 | HG00323.hp2 HG01192.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-262+661_-262+662d others(4): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | ||||||
chr4:174931816 | T | TCACA | 71 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
81 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-262+659_-262+662d others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | ||||||
chr4:174931816 | T | TCACACA | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0220 |
3 | HG00642.hp1 NA19060.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-262+657_-262+662d others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | ||||||
chr4:174931816 | TCA | T | 68 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(65): Show |
85 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-262+661_-262+662d others(4): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174931816 | ||||||
chr4:174931874 | A | G | 1 | a0004c0004t0002g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-262+700A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931874 | |||||||
chr4:174931881 | T | A | 68 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(65): Show |
85 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-262+707T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931881 | |||||||
chr4:174931934 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0016t0002g0039 |
3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-262+760A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174931934 | |||||||
chr4:174932163 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-262+989C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932163 | |||||||
chr4:174932253 | T | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.-262+1079T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932253 | |||||||
chr4:174932297 | G | GA | 67 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(64): Show |
83 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-262+1132dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174932297 | ||||||
chr4:174932308 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0115 a0001c0001t0001g0191 others(1): Show |
6 | HG00423.hp1 HG00621.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-262+1134G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932308 | |||||||
chr4:174932336 | T | C | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-262+1162T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932336 | |||||||
chr4:174932364 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-262+1190G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932364 | |||||||
chr4:174932379 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-262+1205A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932379 | |||||||
chr4:174932384 | A | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(117): Show |
139 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-262+1210A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932384 | |||||||
chr4:174932621 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-262+1447G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932621 | |||||||
chr4:174932872 | G | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-262+1698G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932872 | |||||||
chr4:174932916 | A | C | 1 | a0002c0002t0002g0255 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-262+1742A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932916 | |||||||
chr4:174932966 | C | T | 2 | a0001c0008t0002g0099 a0001c0008t0002g0100 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-262+1792C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174932966 | |||||||
chr4:174933028 | A | G | 3 | a0001c0001t0002g0221 a0005c0007t0002g0222 a0005c0007t0002g0224 |
3 | HG02630.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-262+1854A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933028 | |||||||
chr4:174933270 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-262+2096A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933270 | |||||||
chr4:174933318 | C | T | 67 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(64): Show |
84 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-262+2144C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933318 | |||||||
chr4:174933347 | C | T | 63 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(60): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-262+2173C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933347 | |||||||
chr4:174933362 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-262+2188T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933362 | |||||||
chr4:174933477 | TA | T | 7 | a0001c0001t0002g0226 a0001c0001t0006g0096 a0002c0002t0004g0095 others(4): Show |
8 | HG00544.hp1 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-262+2313delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 174933477 | ||||||
chr4:174933511 | G | C | 3 | a0001c0001t0002g0221 a0005c0007t0002g0222 a0005c0007t0002g0224 |
3 | HG02630.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-262+2337G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933511 | |||||||
chr4:174933515 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-262+2341G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933515 | |||||||
chr4:174933531 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-262+2357A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174933531 | |||||||
chr4:174934002 | T | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.-262+2828T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934002 | |||||||
chr4:174934158 | T | C | 2 | a0001c0001t0002g0265 a0001c0001t0002g0276 |
2 | HG01070.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-261-2775T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934158 | |||||||
chr4:174934183 | C | T | 242 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(239): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-261-2750C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934183 | |||||||
chr4:174934258 | A | G | 63 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(60): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-261-2675A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934258 | |||||||
chr4:174934301 | T | A | 2 | a0001c0001t0002g0003 a0004c0004t0006g0054 |
5 | HG02258.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261-2632T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934301 | |||||||
chr4:174934365 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-261-2568T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934365 | |||||||
chr4:174934421 | T | C | 242 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(239): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-261-2512T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934421 | |||||||
chr4:174934429 | T | G | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-261-2504T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934429 | |||||||
chr4:174934551 | G | A | 3 | a0001c0001t0004g0014 a0001c0001t0005g0177 a0004c0004t0004g0078 |
4 | HG03130.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261-2382G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934551 | |||||||
chr4:174934642 | A | G | 9 | a0001c0001t0002g0226 a0001c0001t0006g0096 a0004c0004t0002g0036 others(6): Show |
10 | HG02109.hp2 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261-2291A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934642 | |||||||
chr4:174934966 | T | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
161 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-261-1967T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174934966 | |||||||
chr4:174935062 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-261-1871T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935062 | |||||||
chr4:174935154 | G | T | 242 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(239): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-261-1779G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935154 | |||||||
chr4:174935160 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0197 others(1): Show |
7 | NA18939.hp2 NA18945.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261-1773C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935160 | |||||||
chr4:174935188 | C | T | 1 | a0004c0004t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-261-1745C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935188 | |||||||
chr4:174935309 | G | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(238): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-261-1624G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935309 | |||||||
chr4:174935442 | T | C | 63 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(60): Show |
80 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-261-1491T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935442 | |||||||
chr4:174935463 | A | C | 1 | a0004c0004t0006g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-261-1470A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935463 | |||||||
chr4:174935491 | A | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-261-1442A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935491 | |||||||
chr4:174935492 | T | C | 6 | a0001c0001t0002g0226 a0001c0001t0006g0096 a0004c0004t0002g0228 others(3): Show |
7 | HG02109.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261-1441T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935492 | |||||||
chr4:174935531 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0016t0002g0039 |
3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-261-1402G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935531 | |||||||
chr4:174935755 | T | C | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-261-1178T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935755 | |||||||
chr4:174935851 | T | G | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-261-1082T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174935851 | |||||||
chr4:174936124 | A | G | 2 | a0002c0002t0003g0074 a0002c0002t0003g0075 |
2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-261-809A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936124 | |||||||
chr4:174936249 | A | C | 42 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0002g0221 others(39): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-261-684A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936249 | |||||||
chr4:174936256 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(238): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-261-677C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936256 | |||||||
chr4:174936297 | T | C | 9 | a0001c0001t0002g0226 a0001c0001t0006g0096 a0004c0004t0002g0036 others(6): Show |
10 | HG02109.hp2 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261-636T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936297 | |||||||
chr4:174936417 | C | T | 1 | a0001c0006t0002g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-261-516C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936417 | |||||||
chr4:174936591 | A | G | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-261-342A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936591 | |||||||
chr4:174936603 | T | G | 1 | a0001c0001t0001g0195 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-261-330T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936603 | |||||||
chr4:174936760 | C | A | 4 | a0004c0004t0002g0228 a0005c0005t0002g0024 a0005c0005t0002g0223 others(1): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261-173C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936760 | |||||||
chr4:174936846 | A | T | 36 | a0001c0001t0002g0136 a0001c0001t0003g0006 a0001c0001t0003g0012 others(33): Show |
40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-261-87A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936846 | |||||||
chr4:174936878 | G | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(238): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-261-55G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | chr4 | 174936878 | |||||||
chr4:174937046 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-181+33A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937046 | |||||||
chr4:174937098 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-181+85C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937098 | |||||||
chr4:174937264 | G | A | 2 | a0004c0015t0002g0227 a0009c0012t0014g0034 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+251G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937264 | |||||||
chr4:174937269 | C | G | 2 | a0005c0007t0002g0222 a0005c0007t0002g0224 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-181+256C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937269 | |||||||
chr4:174937373 | A | G | 1 | a0002c0002t0004g0098 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-181+360A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937373 | |||||||
chr4:174937377 | T | C | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+364T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937377 | |||||||
chr4:174937405 | C | G | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+392C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937405 | |||||||
chr4:174937531 | A | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
101 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-181+518A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937531 | |||||||
chr4:174937552 | A | G | 1 | a0002c0002t0012g0050 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-181+539A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937552 | |||||||
chr4:174937645 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(61): Show |
81 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-181+632C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937645 | |||||||
chr4:174937757 | G | C | 244 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(241): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-181+744G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937757 | |||||||
chr4:174937837 | A | T | 1 | a0001c0001t0003g0047 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-181+824A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937837 | |||||||
chr4:174937995 | G | A | 242 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(239): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-181+982G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174937995 | |||||||
chr4:174938186 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0189 |
2 | NA19000.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-181+1173A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938186 | |||||||
chr4:174938222 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-181+1209A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938222 | |||||||
chr4:174938231 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(61): Show |
81 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-181+1218C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938231 | |||||||
chr4:174938275 | T | C | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+1262T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938275 | |||||||
chr4:174938461 | A | G | 44 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(41): Show |
51 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.-181+1448A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938461 | |||||||
chr4:174938509 | G | A | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+1496G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938509 | |||||||
chr4:174938553 | GTTTCATA others(9): Show |
G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0009t0013g0041 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+1552_-181+156 others(20): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174938553 | ||||||
chr4:174938572 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(61): Show |
81 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-181+1559T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938572 | |||||||
chr4:174938871 | C | T | 2 | a0002c0002t0001g0134 a0002c0002t0001g0188 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-181+1858C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174938871 | |||||||
chr4:174939056 | A | C | 252 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(249): Show |
296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-181+2043A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939056 | |||||||
chr4:174939097 | T | TA | 3 | a0001c0001t0006g0077 a0001c0001t0008g0101 a0001c0001t0008g0102 |
3 | HG03041.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+2085dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174939097 | ||||||
chr4:174939145 | A | G | 3 | a0001c0001t0006g0077 a0001c0001t0008g0101 a0001c0001t0008g0102 |
3 | HG03041.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-181+2132A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939145 | |||||||
chr4:174939173 | T | G | 3 | a0001c0001t0004g0014 a0001c0001t0005g0177 a0004c0004t0004g0078 |
4 | HG03130.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+2160T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939173 | |||||||
chr4:174939177 | A | G | 1 | a0001c0001t0002g0250 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-181+2164A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939177 | |||||||
chr4:174939269 | A | G | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-181+2256A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939269 | |||||||
chr4:174939311 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-181+2298A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939311 | |||||||
chr4:174939405 | G | A | 2 | a0004c0015t0002g0227 a0009c0012t0014g0034 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+2392G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939405 | |||||||
chr4:174939412 | C | A | 38 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0003g0006 others(35): Show |
42 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-181+2399C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939412 | |||||||
chr4:174939746 | A | G | 3 | a0001c0001t0002g0273 a0001c0001t0002g0278 a0004c0004t0002g0269 |
3 | HG00639.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-181+2733A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939746 | |||||||
chr4:174939893 | A | C | 6 | a0001c0001t0004g0014 a0001c0001t0005g0177 a0001c0008t0002g0099 others(3): Show |
7 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-181+2880A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939893 | |||||||
chr4:174939910 | A | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
258 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.-181+2897A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174939910 | |||||||
chr4:174940020 | C | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-181+3007C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940020 | |||||||
chr4:174940064 | T | C | 69 | a0001c0001t0001g0140 a0001c0001t0002g0001 a0001c0001t0002g0011 others(66): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-181+3051T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940064 | |||||||
chr4:174940337 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0003c0003t0001g0110 |
3 | HG02027.hp2 HG02074.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-181+3324A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940337 | |||||||
chr4:174940362 | G | A | 1 | a0002c0002t0001g0120 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-181+3349G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940362 | |||||||
chr4:174940514 | G | GA | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+3507dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174940514 | ||||||
chr4:174940531 | A | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+3518A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940531 | |||||||
chr4:174940567 | CT | C | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+3561delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174940567 | ||||||
chr4:174940688 | G | T | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+3675G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940688 | |||||||
chr4:174940753 | T | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+3740T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940753 | |||||||
chr4:174940847 | T | C | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-181+3834T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940847 | |||||||
chr4:174940898 | C | T | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+3885C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940898 | |||||||
chr4:174940947 | C | T | 1 | a0005c0007t0002g0224 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-181+3934C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174940947 | |||||||
chr4:174941000 | A | G | 1 | a0004c0015t0002g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-181+3987A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941000 | |||||||
chr4:174941056 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0016t0002g0039 |
3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-181+4043G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941056 | |||||||
chr4:174941126 | A | G | 1 | a0002c0002t0004g0093 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-181+4113A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941126 | |||||||
chr4:174941252 | T | C | 3 | a0002c0002t0004g0079 a0002c0002t0004g0082 a0002c0002t0004g0083 |
3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-181+4239T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941252 | |||||||
chr4:174941349 | G | C | 1 | a0004c0004t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-181+4336G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941349 | |||||||
chr4:174941371 | A | T | 41 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0002g0226 others(38): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-181+4358A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941371 | |||||||
chr4:174941763 | T | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+4750T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941763 | |||||||
chr4:174941854 | A | T | 2 | a0004c0015t0002g0227 a0009c0012t0014g0034 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+4841A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941854 | |||||||
chr4:174941864 | C | T | 2 | a0001c0008t0002g0099 a0001c0008t0002g0100 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-181+4851C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174941864 | |||||||
chr4:174942045 | T | G | 1 | a0001c0001t0003g0042 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-181+5032T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942045 | |||||||
chr4:174942307 | C | T | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+5294C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942307 | |||||||
chr4:174942425 | C | T | 2 | a0005c0007t0002g0222 a0005c0007t0002g0224 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-181+5412C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942425 | |||||||
chr4:174942426 | G | A | 5 | a0001c0001t0001g0109 a0002c0002t0003g0061 a0002c0002t0003g0074 others(2): Show |
5 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-181+5413G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942426 | |||||||
chr4:174942470 | G | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+5457G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942470 | |||||||
chr4:174942480 | C | T | 1 | a0004c0004t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-181+5467C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942480 | |||||||
chr4:174942488 | ATCTGCCA others(5): Show |
A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0016t0002g0039 |
3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-181+5477_-181+548 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174942488 | ||||||
chr4:174942562 | T | TG | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+5551dupG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174942562 | ||||||
chr4:174942615 | A | C | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-181+5602A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174942615 | |||||||
chr4:174943046 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+6033A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943046 | |||||||
chr4:174943219 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-181+6206A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943219 | |||||||
chr4:174943259 | A | T | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+6246A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943259 | |||||||
chr4:174943411 | A | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+6398A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943411 | |||||||
chr4:174943482 | G | A | 2 | a0004c0015t0002g0227 a0009c0012t0014g0034 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-181+6469G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943482 | |||||||
chr4:174943526 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-181+6513G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943526 | |||||||
chr4:174943541 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+6528C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943541 | |||||||
chr4:174943590 | G | A | 1 | a0002c0002t0012g0050 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-181+6577G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943590 | |||||||
chr4:174943638 | C | G | 2 | a0003c0003t0002g0256 a0003c0003t0002g0258 |
2 | NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-181+6625C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943638 | |||||||
chr4:174943680 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+6667G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943680 | |||||||
chr4:174943701 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-181+6688C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943701 | |||||||
chr4:174943816 | GA | G | 102 | a0001c0001t0001g0140 a0001c0001t0002g0001 a0001c0001t0002g0003 others(99): Show |
128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-181+6815delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174943816 | ||||||
chr4:174943828 | AG | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+6817delG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174943828 | ||||||
chr4:174943905 | T | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0003c0003t0001g0110 |
3 | HG02027.hp2 HG02074.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-181+6892T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174943905 | |||||||
chr4:174944310 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+7297G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944310 | |||||||
chr4:174944391 | C | G | 41 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0002g0226 others(38): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-181+7378C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944391 | |||||||
chr4:174944442 | A | T | 255 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
300 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-181+7429A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944442 | |||||||
chr4:174944477 | A | G | 1 | a0001c0016t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-181+7464A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944477 | |||||||
chr4:174944540 | T | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-181+7527T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944540 | |||||||
chr4:174944557 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-181+7544T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944557 | |||||||
chr4:174944600 | G | T | 1 | a0002c0002t0001g0103 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-181+7587G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944600 | |||||||
chr4:174944612 | T | C | 255 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
300 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-181+7599T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944612 | |||||||
chr4:174944638 | G | C | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+7625G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944638 | |||||||
chr4:174944968 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-181+7955C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944968 | |||||||
chr4:174944975 | G | T | 41 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0002g0226 others(38): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-181+7962G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174944975 | |||||||
chr4:174945193 | C | A | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+8180C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945193 | |||||||
chr4:174945301 | AG | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+8291delG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174945301 | ||||||
chr4:174945396 | C | A | 1 | a0001c0001t0002g0003 | 4 | HG02258.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+8383C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945396 | |||||||
chr4:174945407 | T | G | 2 | a0001c0001t0005g0270 a0001c0001t0005g0271 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-181+8394T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945407 | |||||||
chr4:174945652 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+8639C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945652 | |||||||
chr4:174945669 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-181+8656A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945669 | |||||||
chr4:174945709 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+8696G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945709 | |||||||
chr4:174945759 | C | T | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+8746C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945759 | |||||||
chr4:174945781 | T | C | 1 | a0003c0003t0001g0121 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-181+8768T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945781 | |||||||
chr4:174945941 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0144 |
2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-181+8928T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174945941 | |||||||
chr4:174946105 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-181+9092G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946105 | |||||||
chr4:174946119 | A | G | 1 | a0001c0001t0003g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-181+9106A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946119 | |||||||
chr4:174946291 | C | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-181+9278C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946291 | |||||||
chr4:174946461 | C | T | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+9448C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946461 | |||||||
chr4:174946587 | G | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+9574G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946587 | |||||||
chr4:174946638 | A | G | 2 | a0001c0001t0003g0045 a0001c0001t0003g0048 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-181+9625A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946638 | |||||||
chr4:174946708 | T | A | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-181+9695T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946708 | |||||||
chr4:174946880 | T | C | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+9867T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174946880 | |||||||
chr4:174947020 | C | T | 4 | a0001c0008t0002g0099 a0001c0008t0002g0100 a0004c0015t0002g0227 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+10007C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947020 | |||||||
chr4:174947043 | A | G | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+10030A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947043 | |||||||
chr4:174947073 | A | G | 41 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0002g0226 others(38): Show |
45 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-181+10060A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947073 | |||||||
chr4:174947132 | C | G | 1 | a0002c0002t0001g0133 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-181+10119C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947132 | |||||||
chr4:174947143 | T | A | 1 | a0004c0004t0002g0228 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-181+10130T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947143 | |||||||
chr4:174947158 | G | A | 3 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 |
3 | HG00738.hp1 HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-181+10145G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947158 | |||||||
chr4:174947285 | T | G | 1 | a0001c0001t0003g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-181+10272T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947285 | |||||||
chr4:174947289 | A | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-181+10276A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947289 | |||||||
chr4:174947337 | T | G | 1 | a0002c0002t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-181+10324T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947337 | |||||||
chr4:174947555 | G | C | 1 | a0001c0001t0004g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-181+10542G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947555 | |||||||
chr4:174947606 | G | A | 69 | a0001c0001t0001g0140 a0001c0001t0002g0001 a0001c0001t0002g0011 others(66): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-181+10593G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947606 | |||||||
chr4:174947884 | A | C | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+10871A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947884 | |||||||
chr4:174947983 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-181+10970T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947983 | |||||||
chr4:174947995 | T | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.-181+10982T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174947995 | |||||||
chr4:174948293 | T | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-181+11280T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948293 | |||||||
chr4:174948472 | G | T | 3 | a0002c0002t0004g0079 a0002c0002t0004g0082 a0002c0002t0004g0083 |
3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-181+11459G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948472 | |||||||
chr4:174948877 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-181+11864G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948877 | |||||||
chr4:174948894 | A | G | 1 | a0001c0001t0007g0164 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-181+11881A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948894 | |||||||
chr4:174948906 | G | T | 1 | a0003c0003t0002g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-181+11893G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174948906 | |||||||
chr4:174949122 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-181+12109C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949122 | |||||||
chr4:174949171 | C | G | 42 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0002g0226 others(39): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-181+12158C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949171 | |||||||
chr4:174949279 | G | A | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+12266G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949279 | |||||||
chr4:174949294 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
103 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-181+12281C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949294 | |||||||
chr4:174949299 | A | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
158 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.-181+12286A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949299 | |||||||
chr4:174949525 | G | A | 36 | a0001c0001t0002g0037 a0001c0001t0002g0136 a0001c0001t0003g0006 others(33): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-181+12512G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949525 | |||||||
chr4:174949589 | G | A | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+12576G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949589 | |||||||
chr4:174949593 | A | G | 39 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(36): Show |
43 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-181+12580A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949593 | |||||||
chr4:174949610 | T | C | 171 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-181+12597T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949610 | |||||||
chr4:174949666 | C | T | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+12653C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949666 | |||||||
chr4:174949693 | T | C | 107 | a0001c0001t0001g0140 a0001c0001t0001g0169 a0001c0001t0001g0213 others(104): Show |
129 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.-181+12680T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949693 | |||||||
chr4:174949711 | C | T | 1 | a0004c0004t0002g0262 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-181+12698C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949711 | |||||||
chr4:174949763 | T | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
170 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-181+12750T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949763 | |||||||
chr4:174949771 | C | T | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
148 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.-181+12758C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949771 | |||||||
chr4:174949793 | C | A | 139 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-181+12780C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949793 | |||||||
chr4:174949827 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-181+12814C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949827 | |||||||
chr4:174949853 | T | C | 8 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0006t0002g0033 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-181+12840T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949853 | |||||||
chr4:174949950 | C | A | 2 | a0001c0008t0002g0099 a0001c0008t0002g0100 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-181+12937C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174949950 | |||||||
chr4:174950298 | A | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
156 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-181+13285A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950298 | |||||||
chr4:174950411 | A | G | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-181+13398A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950411 | |||||||
chr4:174950473 | G | A | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+13460G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950473 | |||||||
chr4:174950843 | G | A | 4 | a0001c0001t0002g0175 a0001c0006t0002g0033 a0001c0006t0002g0035 others(1): Show |
4 | HG02886.hp2 HG03225.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-181+13830G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950843 | |||||||
chr4:174950926 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-181+13913A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950926 | |||||||
chr4:174950980 | G | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-181+13967G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174950980 | |||||||
chr4:174951052 | A | C | 142 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-181+14039A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951052 | |||||||
chr4:174951119 | T | G | 1 | a0001c0001t0003g0042 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-181+14106T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951119 | |||||||
chr4:174951202 | C | A | 127 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(124): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-181+14189C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951202 | |||||||
chr4:174951341 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-181+14328G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951341 | |||||||
chr4:174951411 | C | T | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+14398C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951411 | |||||||
chr4:174951438 | G | T | 1 | a0001c0001t0004g0085 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-181+14425G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951438 | |||||||
chr4:174951489 | A | G | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+14476A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951489 | |||||||
chr4:174951541 | A | G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0249 others(1): Show |
4 | HG01496.hp2 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-181+14528A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951541 | |||||||
chr4:174951715 | A | G | 134 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(131): Show |
165 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-181+14702A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951715 | |||||||
chr4:174951749 | A | G | 80 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(77): Show |
99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-181+14736A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951749 | |||||||
chr4:174951858 | C | T | 1 | a0009c0012t0014g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-181+14845C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951858 | |||||||
chr4:174951899 | T | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+14886T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951899 | |||||||
chr4:174951953 | C | A | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-181+14940C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951953 | |||||||
chr4:174951977 | T | C | 1 | a0001c0001t0005g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-181+14964T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951977 | |||||||
chr4:174951996 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+14983C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174951996 | |||||||
chr4:174952146 | G | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15133G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952146 | |||||||
chr4:174952350 | C | CCA | 21 | a0001c0001t0001g0147 a0001c0001t0001g0194 a0001c0001t0001g0213 others(18): Show |
26 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.-181+15367_-181+15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | ||||||
chr4:174952350 | C | CCACA | 14 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0237 others(11): Show |
16 | HG01109.hp2 HG01496.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-181+15365_-181+15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | ||||||
chr4:174952350 | CCA | C | 74 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0106 others(71): Show |
96 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-181+15367_-181+15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | ||||||
chr4:174952350 | CCACA | C | 9 | a0001c0001t0002g0175 a0001c0001t0006g0077 a0001c0001t0008g0101 others(6): Show |
9 | HG01891.hp1 HG02622.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-181+15365_-181+15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | ||||||
chr4:174952350 | CCACACA | C | 13 | a0001c0001t0001g0192 a0001c0001t0002g0221 a0001c0001t0002g0265 others(10): Show |
14 | HG00408.hp2 HG00642.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-181+15363_-181+15 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174952350 | ||||||
chr4:174952444 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15431G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952444 | |||||||
chr4:174952713 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15700C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952713 | |||||||
chr4:174952739 | AG | A | 120 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(117): Show |
149 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-181+15727delG | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952739 | |||||||
chr4:174952786 | T | C | 2 | a0002c0002t0001g0134 a0002c0002t0001g0188 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-181+15773T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952786 | |||||||
chr4:174952846 | A | T | 120 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(117): Show |
149 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-181+15833A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952846 | |||||||
chr4:174952861 | C | T | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-181+15848C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952861 | |||||||
chr4:174952992 | A | G | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+15979A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174952992 | |||||||
chr4:174953012 | C | T | 1 | a0002c0002t0004g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-181+15999C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953012 | |||||||
chr4:174953142 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16129C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953142 | |||||||
chr4:174953172 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16159G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953172 | |||||||
chr4:174953214 | A | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16201A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953214 | |||||||
chr4:174953216 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16203G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953216 | |||||||
chr4:174953229 | T | G | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16216T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953229 | |||||||
chr4:174953255 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16242T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953255 | |||||||
chr4:174953280 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16267T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953280 | |||||||
chr4:174953333 | A | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16320A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953333 | |||||||
chr4:174953368 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-181+16355A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953368 | |||||||
chr4:174953426 | G | T | 1 | a0001c0001t0003g0056 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-181+16413G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953426 | |||||||
chr4:174953574 | T | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16561T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953574 | |||||||
chr4:174953722 | T | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16709T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953722 | |||||||
chr4:174953775 | A | G | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16762A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953775 | |||||||
chr4:174953845 | G | A | 3 | a0001c0001t0002g0175 a0001c0006t0002g0033 a0001c0006t0002g0035 |
3 | HG03225.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-181+16832G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953845 | |||||||
chr4:174953913 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16900C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953913 | |||||||
chr4:174953991 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16978T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953991 | |||||||
chr4:174953999 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+16986G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174953999 | |||||||
chr4:174954079 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17066T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954079 | |||||||
chr4:174954093 | C | T | 3 | a0001c0001t0002g0175 a0001c0006t0002g0033 a0001c0006t0002g0035 |
3 | HG03225.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-181+17080C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954093 | |||||||
chr4:174954207 | A | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17194A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954207 | |||||||
chr4:174954239 | A | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17226A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954239 | |||||||
chr4:174954248 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17235C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954248 | |||||||
chr4:174954252 | G | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17239G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954252 | |||||||
chr4:174954335 | C | T | 1 | a0001c0001t0005g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-181+17322C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954335 | |||||||
chr4:174954453 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17440T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954453 | |||||||
chr4:174954474 | G | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17461G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954474 | |||||||
chr4:174954477 | T | C | 122 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(119): Show |
152 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-181+17464T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954477 | |||||||
chr4:174954496 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0226 a0001c0001t0006g0096 |
6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-181+17483C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954496 | |||||||
chr4:174954566 | A | G | 1 | a0003c0003t0002g0183 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-181+17553A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954566 | |||||||
chr4:174954604 | C | T | 1 | a0001c0009t0011g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-181+17591C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954604 | |||||||
chr4:174954635 | T | C | 6 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(3): Show |
6 | HG01255.hp1 HG02523.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-181+17622T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954635 | |||||||
chr4:174954737 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-181+17724G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954737 | |||||||
chr4:174954863 | A | G | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+17850A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954863 | |||||||
chr4:174954911 | C | G | 1 | a0003c0003t0001g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-181+17898C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174954911 | |||||||
chr4:174955002 | A | C | 132 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(129): Show |
163 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.-181+17989A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955002 | |||||||
chr4:174955083 | AT | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18078delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174955083 | ||||||
chr4:174955172 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18159T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955172 | |||||||
chr4:174955173 | G | A | 1 | a0004c0004t0002g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-181+18160G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955173 | |||||||
chr4:174955198 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18185G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955198 | |||||||
chr4:174955205 | A | G | 2 | a0001c0001t0001g0161 a0003c0003t0001g0214 |
2 | HG01975.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-181+18192A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955205 | |||||||
chr4:174955222 | G | A | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-181+18209G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955222 | |||||||
chr4:174955322 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18309T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955322 | |||||||
chr4:174955443 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-181+18430G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955443 | |||||||
chr4:174955516 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18503C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955516 | |||||||
chr4:174955661 | C | CTTATT | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18651_-181+18 others(11): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174955661 | ||||||
chr4:174955727 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+18714G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955727 | |||||||
chr4:174955901 | C | T | 81 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(78): Show |
100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-181+18888C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174955901 | |||||||
chr4:174956025 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+19012T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956025 | |||||||
chr4:174956044 | A | G | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-181+19031A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956044 | |||||||
chr4:174956150 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-181+19137C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956150 | |||||||
chr4:174956209 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-19137G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956209 | |||||||
chr4:174956227 | A | C | 3 | a0002c0002t0004g0079 a0002c0002t0004g0082 a0002c0002t0004g0083 |
3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-180-19119A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956227 | |||||||
chr4:174956327 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-180-19019G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956327 | |||||||
chr4:174956406 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18940C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956406 | |||||||
chr4:174956420 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18926C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956420 | |||||||
chr4:174956440 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18906C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956440 | |||||||
chr4:174956445 | C | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0249 |
3 | HG01496.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-180-18901C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956445 | |||||||
chr4:174956448 | T | G | 1 | a0001c0001t0002g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-180-18898T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956448 | |||||||
chr4:174956475 | G | GGT | 3 | a0003c0003t0001g0196 a0003c0003t0002g0258 a0004c0004t0002g0036 |
3 | HG02572.hp1 NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-180-18854_-180-18 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174956475 | ||||||
chr4:174956508 | T | G | 121 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(118): Show |
151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-180-18838T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956508 | |||||||
chr4:174956510 | G | T | 121 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(118): Show |
151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-180-18836G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956510 | |||||||
chr4:174956513 | A | T | 121 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(118): Show |
151 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-180-18833A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956513 | |||||||
chr4:174956522 | GA | G | 122 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(119): Show |
152 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-180-18816delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174956522 | ||||||
chr4:174956551 | A | G | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-18795A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956551 | |||||||
chr4:174956654 | A | G | 1 | a0001c0016t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-18692A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956654 | |||||||
chr4:174956742 | C | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-18604C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956742 | |||||||
chr4:174956766 | A | G | 3 | a0001c0001t0002g0175 a0001c0006t0002g0033 a0001c0006t0002g0035 |
3 | HG03225.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-180-18580A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956766 | |||||||
chr4:174956887 | A | G | 76 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(73): Show |
92 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.-180-18459A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956887 | |||||||
chr4:174956905 | A | C | 2 | a0001c0001t0008g0101 a0001c0001t0008g0102 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-180-18441A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174956905 | |||||||
chr4:174957013 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-180-18333A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957013 | |||||||
chr4:174957413 | C | T | 3 | a0001c0001t0008g0101 a0001c0001t0008g0102 a0004c0004t0002g0228 |
3 | HG03130.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-180-17933C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957413 | |||||||
chr4:174957414 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-17932C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957414 | |||||||
chr4:174957542 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-180-17804A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957542 | |||||||
chr4:174957577 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-180-17769C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957577 | |||||||
chr4:174957767 | T | C | 122 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(119): Show |
152 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-180-17579T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957767 | |||||||
chr4:174957771 | T | C | 1 | a0001c0001t0005g0270 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-180-17575T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174957771 | |||||||
chr4:174958018 | A | T | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-17328A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958018 | |||||||
chr4:174958064 | A | T | 1 | a0001c0001t0007g0160 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-180-17282A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958064 | |||||||
chr4:174958120 | G | A | 2 | a0002c0002t0001g0103 a0002c0002t0001g0127 |
2 | NA18970.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-180-17226G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958120 | |||||||
chr4:174958135 | T | G | 2 | a0001c0008t0002g0099 a0001c0008t0002g0100 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-180-17211T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958135 | |||||||
chr4:174958184 | C | T | 2 | a0001c0001t0003g0071 a0001c0001t0003g0073 |
2 | HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-180-17162C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958184 | |||||||
chr4:174958243 | G | A | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-17103G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958243 | |||||||
chr4:174958245 | G | GA | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-17101_-180-17 others(7): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958245 | |||||||
chr4:174958356 | A | G | 130 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(127): Show |
161 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-180-16990A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958356 | |||||||
chr4:174958472 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16874C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958472 | |||||||
chr4:174958527 | C | T | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16819C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958527 | |||||||
chr4:174958608 | C | T | 1 | a0001c0001t0004g0091 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-180-16738C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958608 | |||||||
chr4:174958643 | A | C | 1 | a0009c0012t0014g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-180-16703A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958643 | |||||||
chr4:174958726 | CTTTT | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
17 | HG00323.hp1 HG00323.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-180-16616_-180-16 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174958726 | ||||||
chr4:174958727 | T | C | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16619T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958727 | |||||||
chr4:174958750 | A | G | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16596A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958750 | |||||||
chr4:174958791 | T | A | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-180-16555T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958791 | |||||||
chr4:174958859 | A | C | 1 | a0001c0006t0002g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-180-16487A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174958859 | |||||||
chr4:174958983 | A | ATTG | 123 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(120): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-180-16361_-180-16 others(9): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174958983 | ||||||
chr4:174959044 | A | T | 1 | a0001c0001t0002g0277 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-180-16302A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959044 | |||||||
chr4:174959205 | T | A | 7 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(4): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-16141T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959205 | |||||||
chr4:174959317 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-180-16029C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959317 | |||||||
chr4:174959317 | C | T | 3 | a0001c0001t0004g0014 a0004c0004t0004g0078 a0004c0004t0006g0054 |
4 | HG03098.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-16029C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959317 | |||||||
chr4:174959340 | T | C | 7 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(4): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-16006T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959340 | |||||||
chr4:174959417 | A | G | 9 | a0001c0001t0002g0268 a0004c0004t0002g0029 a0004c0004t0002g0174 others(6): Show |
10 | HG00741.hp1 HG01433.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-15929A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959417 | |||||||
chr4:174959457 | C | CTG | 53 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(50): Show |
67 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-15863_-180-15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | ||||||
chr4:174959457 | C | CTGTG | 28 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0189 others(25): Show |
33 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-180-15865_-180-15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | ||||||
chr4:174959457 | CTG | C | 15 | a0001c0001t0002g0175 a0001c0001t0002g0246 a0001c0001t0002g0252 others(12): Show |
16 | HG00639.hp1 HG01109.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.-180-15863_-180-15 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | ||||||
chr4:174959457 | CTGTG | C | 4 | a0001c0016t0002g0039 a0002c0002t0004g0002 a0003c0003t0002g0135 others(1): Show |
8 | HG02135.hp1 HG02818.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.-180-15865_-180-15 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959457 | ||||||
chr4:174959477 | GTGTGTGT others(1): Show |
G | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-15853_-180-15 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174959477 | ||||||
chr4:174959485 | T | G | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-15861T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959485 | |||||||
chr4:174959503 | C | G | 1 | a0001c0008t0002g0100 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-180-15843C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959503 | |||||||
chr4:174959504 | T | C | 1 | a0001c0016t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-15842T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959504 | |||||||
chr4:174959604 | A | G | 7 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(4): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-15742A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959604 | |||||||
chr4:174959915 | G | T | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-15431G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959915 | |||||||
chr4:174959954 | G | A | 20 | a0001c0001t0002g0268 a0001c0001t0004g0014 a0004c0004t0001g0202 others(17): Show |
24 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-180-15392G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174959954 | |||||||
chr4:174960025 | G | A | 1 | a0001c0001t0007g0164 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-180-15321G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960025 | |||||||
chr4:174960154 | T | C | 7 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(4): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-15192T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960154 | |||||||
chr4:174960191 | G | C | 1 | a0001c0001t0002g0240 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-180-15155G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960191 | |||||||
chr4:174960193 | G | T | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-15153G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960193 | |||||||
chr4:174960477 | A | G | 2 | a0001c0016t0002g0039 a0004c0004t0002g0036 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-180-14869A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960477 | |||||||
chr4:174960580 | T | C | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-14766T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960580 | |||||||
chr4:174960685 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-180-14661T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960685 | |||||||
chr4:174960789 | T | C | 7 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(4): Show |
8 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-14557T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960789 | |||||||
chr4:174960934 | T | C | 2 | a0004c0004t0009g0233 a0004c0004t0009g0234 |
2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-180-14412T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960934 | |||||||
chr4:174960990 | C | T | 128 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(125): Show |
159 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.-180-14356C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174960990 | |||||||
chr4:174961040 | A | G | 1 | a0001c0016t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-14306A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961040 | |||||||
chr4:174961226 | A | G | 14 | a0001c0001t0005g0270 a0001c0001t0005g0271 a0001c0009t0011g0097 others(11): Show |
18 | HG00544.hp1 HG01123.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-180-14120A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961226 | |||||||
chr4:174961319 | T | C | 3 | a0005c0005t0002g0024 a0005c0005t0002g0223 a0005c0005t0002g0225 |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-14027T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961319 | |||||||
chr4:174961728 | G | A | 129 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(126): Show |
160 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-180-13618G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961728 | |||||||
chr4:174961794 | A | G | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-13552A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961794 | |||||||
chr4:174961938 | T | C | 14 | a0001c0001t0005g0270 a0001c0001t0005g0271 a0001c0009t0011g0097 others(11): Show |
18 | HG00544.hp1 HG01123.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-180-13408T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174961938 | |||||||
chr4:174962034 | G | A | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-13312G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962034 | |||||||
chr4:174962187 | C | G | 2 | a0001c0008t0002g0099 a0001c0008t0002g0100 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-180-13159C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962187 | |||||||
chr4:174962249 | T | C | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0148 others(5): Show |
10 | HG01255.hp2 HG01346.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-13097T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962249 | |||||||
chr4:174962264 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0250 |
2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-180-13082T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962264 | |||||||
chr4:174962293 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-180-13053T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962293 | |||||||
chr4:174962318 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-180-13028T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962318 | |||||||
chr4:174962319 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-180-13027G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962319 | |||||||
chr4:174962380 | G | C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0226 a0001c0001t0006g0096 others(2): Show |
8 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-180-12966G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962380 | |||||||
chr4:174962396 | C | T | 2 | a0001c0006t0002g0033 a0001c0006t0002g0035 |
2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-12950C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962396 | |||||||
chr4:174962441 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0249 |
3 | HG01496.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-180-12905A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962441 | |||||||
chr4:174962444 | A | G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0249 others(1): Show |
4 | HG01496.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-12902A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962444 | |||||||
chr4:174962482 | A | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-180-12864A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962482 | |||||||
chr4:174962506 | C | T | 2 | a0001c0001t0001g0207 a0004c0004t0002g0027 |
3 | HG01109.hp1 NA18906.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-180-12840C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962506 | |||||||
chr4:174962511 | C | CA | 22 | a0001c0001t0001g0141 a0001c0001t0002g0237 a0001c0001t0002g0265 others(19): Show |
22 | HG01070.hp2 HG01928.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-180-12818dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174962511 | ||||||
chr4:174962511 | CA | C | 7 | a0001c0001t0001g0199 a0001c0001t0002g0003 a0001c0001t0002g0226 others(4): Show |
10 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-180-12818delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174962511 | ||||||
chr4:174962540 | T | G | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-12806T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962540 | |||||||
chr4:174962784 | GA | G | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-12553delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174962784 | ||||||
chr4:174962994 | A | G | 135 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(132): Show |
165 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-180-12352A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174962994 | |||||||
chr4:174963097 | A | T | 1 | a0002c0002t0001g0108 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-180-12249A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963097 | |||||||
chr4:174963661 | C | T | 2 | a0001c0001t0006g0077 a0009c0012t0014g0034 |
2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-180-11685C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963661 | |||||||
chr4:174963667 | G | A | 111 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(108): Show |
135 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-180-11679G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963667 | |||||||
chr4:174963690 | AT | A | 111 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(108): Show |
135 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-180-11648delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174963690 | ||||||
chr4:174963841 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-180-11505C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963841 | |||||||
chr4:174963882 | G | C | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-11464G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963882 | |||||||
chr4:174963891 | G | A | 19 | a0001c0001t0002g0268 a0004c0004t0001g0202 a0004c0004t0002g0027 others(16): Show |
22 | HG00741.hp1 HG01109.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-180-11455G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963891 | |||||||
chr4:174963905 | G | A | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-11441G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963905 | |||||||
chr4:174963922 | A | G | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-11424A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963922 | |||||||
chr4:174963951 | G | A | 1 | a0009c0012t0014g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-180-11395G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174963951 | |||||||
chr4:174964087 | A | C | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-11259A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964087 | |||||||
chr4:174964238 | T | A | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-11108T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964238 | |||||||
chr4:174964289 | A | T | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-11057A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964289 | |||||||
chr4:174964319 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-180-11027A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964319 | |||||||
chr4:174964426 | C | T | 6 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-10920C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964426 | |||||||
chr4:174964508 | A | G | 2 | a0002c0002t0001g0131 a0002c0002t0001g0133 |
2 | NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-180-10838A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964508 | |||||||
chr4:174964548 | A | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0140 a0001c0001t0015g0116 |
3 | HG00558.hp2 HG00673.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-180-10798A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964548 | |||||||
chr4:174964882 | GTGTT | G | 4 | a0001c0001t0001g0208 a0001c0001t0002g0003 a0001c0008t0002g0099 others(1): Show |
7 | HG01891.hp1 HG02132.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180-10461_-180-10 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174964882 | ||||||
chr4:174964899 | T | C | 1 | a0001c0016t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-180-10447T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964899 | |||||||
chr4:174964912 | T | A | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-10434T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964912 | |||||||
chr4:174964926 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-180-10420C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174964926 | |||||||
chr4:174965167 | G | T | 1 | a0001c0001t0003g0013 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-180-10179G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965167 | |||||||
chr4:174965244 | A | AAG | 118 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0106 others(115): Show |
143 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-180-10092_-180-10 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965244 | ||||||
chr4:174965412 | A | T | 1 | a0002c0002t0003g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-180-9934A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965412 | |||||||
chr4:174965446 | A | C | 104 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0106 others(101): Show |
127 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-180-9900A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965446 | |||||||
chr4:174965454 | T | C | 1 | a0002c0002t0001g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-180-9892T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965454 | |||||||
chr4:174965457 | G | C | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-180-9889G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965457 | |||||||
chr4:174965484 | C | CATCT | 85 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(82): Show |
100 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-180-9826_-180-982 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | ||||||
chr4:174965484 | C | CATCTATC others(1): Show |
45 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0143 others(42): Show |
52 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-180-9830_-180-982 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | ||||||
chr4:174965484 | C | CATCTATC others(5): Show |
2 | a0001c0001t0003g0068 a0006c0010t0003g0067 |
2 | HG01981.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-180-9834_-180-982 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | ||||||
chr4:174965484 | CATCT | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0180 others(9): Show |
15 | HG00609.hp2 HG01074.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-180-9826_-180-982 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | ||||||
chr4:174965484 | CATCTATC others(1): Show |
C | 4 | a0001c0001t0002g0257 a0001c0001t0003g0047 a0001c0001t0006g0077 others(1): Show |
4 | HG00642.hp2 HG00741.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-9830_-180-982 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965484 | ||||||
chr4:174965508 | T | TATCTATC others(8): Show |
1 | a0001c0001t0002g0221 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-180-9830_-180-981 others(19): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174965508 | ||||||
chr4:174965537 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-180-9809T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965537 | |||||||
chr4:174965665 | C | T | 1 | a0001c0001t0005g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-180-9681C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965665 | |||||||
chr4:174965686 | A | T | 2 | a0001c0001t0002g0221 a0004c0004t0002g0228 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-180-9660A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965686 | |||||||
chr4:174965701 | C | T | 3 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0009c0012t0014g0034 |
3 | HG03225.hp2 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-9645C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965701 | |||||||
chr4:174965759 | T | C | 129 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(126): Show |
157 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-180-9587T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174965759 | |||||||
chr4:174966064 | C | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0249 others(1): Show |
4 | HG01496.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-9282C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966064 | |||||||
chr4:174966096 | G | A | 1 | a0002c0002t0002g0259 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-180-9250G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966096 | |||||||
chr4:174966107 | A | G | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-9239A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966107 | |||||||
chr4:174966311 | G | C | 141 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(138): Show |
172 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-180-9035G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966311 | |||||||
chr4:174966312 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-180-9034C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966312 | |||||||
chr4:174966313 | A | T | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-9033A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966313 | |||||||
chr4:174966328 | T | C | 5 | a0001c0001t0002g0026 a0001c0001t0002g0117 a0001c0001t0002g0118 others(2): Show |
6 | HG02040.hp2 NA18949.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-9018T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966328 | |||||||
chr4:174966329 | T | C | 1 | a0008c0014t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-180-9017T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966329 | |||||||
chr4:174966332 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-180-9014A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966332 | |||||||
chr4:174966493 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-180-8853G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966493 | |||||||
chr4:174966519 | C | T | 2 | a0001c0001t0003g0045 a0001c0001t0003g0048 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-180-8827C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966519 | |||||||
chr4:174966598 | A | T | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-8748A>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966598 | |||||||
chr4:174966708 | G | A | 84 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(81): Show |
102 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-180-8638G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966708 | |||||||
chr4:174966747 | T | G | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-8599T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966747 | |||||||
chr4:174966788 | C | T | 2 | a0001c0008t0002g0099 a0001c0008t0002g0100 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-180-8558C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966788 | |||||||
chr4:174966872 | A | G | 2 | a0001c0001t0002g0221 a0001c0016t0002g0039 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-180-8474A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966872 | |||||||
chr4:174966995 | C | T | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-8351C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174966995 | |||||||
chr4:174967046 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-180-8300G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967046 | |||||||
chr4:174967321 | TTTATTA | T | 52 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(49): Show |
67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-8015_-180-801 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174967321 | ||||||
chr4:174967355 | T | C | 52 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(49): Show |
67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-7991T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967355 | |||||||
chr4:174967523 | TA | T | 52 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(49): Show |
67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.-180-7822delA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967523 | |||||||
chr4:174967576 | T | G | 8 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0005c0005t0002g0024 others(5): Show |
9 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-180-7770T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967576 | |||||||
chr4:174967590 | G | A | 1 | a0004c0015t0002g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-180-7756G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967590 | |||||||
chr4:174967591 | G | GA | 3 | a0001c0001t0001g0169 a0001c0001t0003g0071 a0001c0001t0003g0073 |
3 | HG02738.hp1 HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-180-7752dupA | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174967591 | ||||||
chr4:174967829 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-180-7517T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174967829 | |||||||
chr4:174968123 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-180-7223C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968123 | |||||||
chr4:174968154 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-180-7192T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968154 | |||||||
chr4:174968646 | C | A | 25 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0004c0004t0001g0202 others(22): Show |
28 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-180-6700C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968646 | |||||||
chr4:174968771 | C | A | 1 | a0001c0001t0003g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-180-6575C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968771 | |||||||
chr4:174968771 | C | CA | 4 | a0001c0001t0001g0155 a0001c0001t0001g0169 a0001c0001t0003g0051 others(1): Show |
4 | HG00323.hp1 HG01099.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-6575_-180-657 others(5): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968771 | |||||||
chr4:174968771 | C | CCA | 22 | a0001c0001t0001g0156 a0001c0001t0001g0184 a0001c0001t0002g0136 others(19): Show |
23 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-180-6540_-180-653 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | C | CCACA | 3 | a0001c0001t0001g0145 a0001c0001t0003g0013 a0001c0001t0003g0070 |
4 | HG01884.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180-6542_-180-653 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | CCA | C | 8 | a0001c0001t0001g0152 a0001c0001t0001g0215 a0001c0001t0002g0246 others(5): Show |
8 | HG00438.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-180-6540_-180-653 others(6): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | CCACA | C | 7 | a0001c0001t0001g0159 a0001c0001t0002g0226 a0001c0001t0002g0268 others(4): Show |
7 | HG01243.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-6542_-180-653 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | CCACACA | C | 4 | a0001c0001t0002g0221 a0005c0005t0002g0024 a0005c0005t0002g0223 others(1): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-180-6544_-180-653 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | CCACACAC others(1): Show |
C | 7 | a0001c0001t0002g0003 a0001c0006t0002g0033 a0001c0006t0002g0035 others(4): Show |
10 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-180-6546_-180-653 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | CCACACAC others(3): Show |
C | 12 | a0001c0001t0001g0124 a0001c0001t0002g0038 a0001c0001t0002g0040 others(9): Show |
12 | HG01255.hp1 HG01496.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-180-6548_-180-653 others(14): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968771 | CCACACAC others(5): Show |
C | 119 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0125 others(116): Show |
146 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-180-6550_-180-653 others(16): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174968771 | ||||||
chr4:174968773 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-180-6573A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968773 | |||||||
chr4:174968824 | A | G | 42 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0020 others(39): Show |
51 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-180-6522A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968824 | |||||||
chr4:174968976 | G | A | 139 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(136): Show |
170 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.-180-6370G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174968976 | |||||||
chr4:174969008 | A | AAAAG | 90 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(87): Show |
109 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-180-6332_-180-632 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174969008 | ||||||
chr4:174969367 | T | C | 2 | a0001c0006t0002g0033 a0001c0006t0002g0035 |
2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-5979T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969367 | |||||||
chr4:174969601 | A | G | 17 | a0002c0002t0001g0016 a0002c0002t0001g0105 a0002c0002t0003g0044 others(14): Show |
22 | HG00544.hp1 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-180-5745A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969601 | |||||||
chr4:174969679 | A | G | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-5667A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969679 | |||||||
chr4:174969722 | T | C | 55 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(52): Show |
70 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-180-5624T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969722 | |||||||
chr4:174969944 | T | G | 1 | a0001c0001t0002g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-180-5402T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969944 | |||||||
chr4:174969954 | A | C | 7 | a0001c0001t0002g0268 a0001c0001t0002g0273 a0001c0001t0002g0278 others(4): Show |
7 | HG02647.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-5392A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174969954 | |||||||
chr4:174970013 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-180-5333C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970013 | |||||||
chr4:174970021 | C | G | 1 | a0002c0002t0001g0108 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-180-5325C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970021 | |||||||
chr4:174970145 | G | T | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-5201G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970145 | |||||||
chr4:174970162 | A | G | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-180-5184A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970162 | |||||||
chr4:174970192 | G | C | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-5154G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970192 | |||||||
chr4:174970197 | AT | A | 25 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0004c0004t0001g0202 others(22): Show |
28 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-180-5147delT | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174970197 | ||||||
chr4:174970253 | T | C | 2 | a0004c0004t0002g0036 a0004c0004t0002g0228 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-180-5093T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970253 | |||||||
chr4:174970341 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0199 |
3 | NA18945.hp1 NA18947.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-180-5005G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970341 | |||||||
chr4:174970446 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-180-4900C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970446 | |||||||
chr4:174970563 | C | T | 43 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0020 others(40): Show |
52 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-180-4783C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970563 | |||||||
chr4:174970794 | C | T | 55 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(52): Show |
70 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-180-4552C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970794 | |||||||
chr4:174970897 | T | C | 1 | a0001c0009t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-180-4449T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970897 | |||||||
chr4:174970991 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0209 |
2 | HG03453.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-180-4355A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174970991 | |||||||
chr4:174971263 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-180-4083G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971263 | |||||||
chr4:174971415 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-180-3931C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971415 | |||||||
chr4:174971425 | TTTTG | T | 43 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0020 others(40): Show |
52 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-180-3917_-180-391 others(8): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | 174971425 | ||||||
chr4:174971537 | C | T | 25 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0004c0004t0001g0202 others(22): Show |
28 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-180-3809C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971537 | |||||||
chr4:174971581 | G | T | 80 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(77): Show |
98 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-180-3765G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971581 | |||||||
chr4:174971738 | T | G | 44 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0020 others(41): Show |
53 | HG00544.hp1 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-180-3608T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971738 | |||||||
chr4:174971800 | T | A | 1 | a0001c0001t0002g0026 | 2 | HG02040.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-180-3546T>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174971800 | |||||||
chr4:174972014 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0020 a0002c0002t0001g0021 others(23): Show |
30 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-180-3332G>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972014 | |||||||
chr4:174972152 | T | G | 1 | a0004c0004t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-180-3194T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972152 | |||||||
chr4:174972212 | G | C | 1 | a0001c0001t0002g0250 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-180-3134G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972212 | |||||||
chr4:174972340 | C | A | 5 | a0005c0005t0002g0024 a0005c0005t0002g0223 a0005c0005t0002g0225 others(2): Show |
6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-3006C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972340 | |||||||
chr4:174972710 | T | C | 1 | a0004c0004t0006g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-2636T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972710 | |||||||
chr4:174972830 | C | A | 3 | a0001c0001t0002g0221 a0001c0001t0006g0077 a0001c0016t0002g0039 |
3 | HG02818.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-180-2516C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174972830 | |||||||
chr4:174973015 | C | T | 5 | a0005c0005t0002g0024 a0005c0005t0002g0223 a0005c0005t0002g0225 others(2): Show |
6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-2331C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973015 | |||||||
chr4:174973195 | T | C | 2 | a0001c0006t0002g0033 a0001c0006t0002g0035 |
2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-180-2151T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973195 | |||||||
chr4:174973229 | C | A | 88 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(85): Show |
106 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-180-2117C>A | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973229 | |||||||
chr4:174973237 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0140 |
2 | HG00558.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-180-2109G>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973237 | |||||||
chr4:174973247 | C | G | 131 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(128): Show |
158 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.-180-2099C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973247 | |||||||
chr4:174973682 | T | G | 5 | a0005c0005t0002g0024 a0005c0005t0002g0223 a0005c0005t0002g0225 others(2): Show |
6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-1664T>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973682 | |||||||
chr4:174973776 | C | G | 1 | a0001c0001t0002g0250 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-180-1570C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973776 | |||||||
chr4:174973835 | C | T | 80 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(77): Show |
98 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-180-1511C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973835 | |||||||
chr4:174973903 | C | T | 2 | a0001c0009t0011g0097 a0001c0009t0013g0041 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-180-1443C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973903 | |||||||
chr4:174973921 | G | C | 140 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(137): Show |
171 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-180-1425G>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174973921 | |||||||
chr4:174974156 | A | G | 3 | a0001c0001t0002g0003 a0001c0008t0002g0099 a0001c0008t0002g0100 |
6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-180-1190A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974156 | |||||||
chr4:174974251 | A | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0148 others(5): Show |
10 | HG00323.hp2 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-180-1095A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974251 | |||||||
chr4:174974413 | A | C | 5 | a0005c0005t0002g0024 a0005c0005t0002g0223 a0005c0005t0002g0225 others(2): Show |
6 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-180-933A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974413 | |||||||
chr4:174974483 | C | G | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0249 others(1): Show |
4 | HG01496.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180-863C>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974483 | |||||||
chr4:174974484 | C | T | 2 | a0005c0007t0002g0222 a0005c0007t0002g0224 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-180-862C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974484 | |||||||
chr4:174974747 | A | C | 55 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0124 others(52): Show |
70 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-180-599A>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974747 | |||||||
chr4:174974798 | C | T | 3 | a0002c0002t0004g0079 a0002c0002t0004g0082 a0002c0002t0004g0083 |
3 | HG01123.hp1 HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-180-548C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974798 | |||||||
chr4:174974832 | T | C | 3 | a0001c0001t0002g0221 a0001c0001t0006g0077 a0001c0016t0002g0039 |
3 | HG02818.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-180-514T>C | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174974832 | |||||||
chr4:174975029 | A | G | 1 | a0004c0004t0006g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-180-317A>G | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174975029 | |||||||
chr4:174975106 | C | T | 1 | a0003c0003t0002g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-180-240C>T | ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | 174975106 |