Item | Value |
---|---|
geneid | 7447 |
ensemblid | ENSG00000163032.12 |
hgncid | 12722 |
symbol | VSNL1 |
name | visinin like 1 |
refseq_nuc | NM_003385.5 |
refseq_prot | NP_003376.2 |
ensembl_nuc | ENST00000295156.9 |
ensembl_prot | ENSP00000295156.4 |
mane_status | MANE Select |
chr | chr2 |
start | 17540696 |
end | 17657018 |
strand | + |
ver | v1.2 |
region | chr2:17540696-17657018 |
region5000 | chr2:17535696-17662018 |
regionname0 | VSNL1_chr2_17540696_17657018 |
regionname5000 | VSNL1_chr2_17535696_17662018 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 573 | 232 | 82 | 54 | 54 | 16 | 24 | VSNL1_chr2_17535696_17662018 | VSNL1 | ATGGG others(568): Show |
chr2 | 17535696 | 17662018 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2424 | 40 | 3 | 8 | 26 | 0 | 3 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2419): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0002 | 0/0 | 2432 | 19 | 1 | 6 | 2 | 6 | 4 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2427): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0003 | 0/0 | 2432 | 13 | 6 | 5 | 1 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2427): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0004 | 0/0 | 2430 | 12 | 8 | 1 | 0 | 2 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2425): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0005 | 1/0 | 2428 | 11 | 0 | 5 | 2 | 2 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2423): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0006 | 0/0 | 2428 | 11 | 8 | 3 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2423): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0007 | 0/0 | 2427 | 9 | 6 | 3 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2422): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0008 | 0/0 | 2424 | 8 | 7 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2419): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0009 | 0/0 | 2430 | 8 | 0 | 2 | 4 | 1 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2425): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0010 | 0/0 | 2420 | 7 | 6 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2415): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0011 | 0/0 | 2423 | 7 | 1 | 4 | 0 | 0 | 2 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2418): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0012 | 0/0 | 2434 | 7 | 0 | 0 | 3 | 0 | 4 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2429): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0013 | 0/1 | 2436 | 7 | 0 | 5 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2431): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0014 | 0/0 | 2434 | 6 | 1 | 2 | 2 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2429): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0015 | 0/0 | 2426 | 5 | 0 | 2 | 1 | 1 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2421): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0016 | 0/0 | 2428 | 5 | 1 | 1 | 3 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2423): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0017 | 0/0 | 2432 | 5 | 5 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2427): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0018 | 0/0 | 2436 | 5 | 0 | 0 | 5 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2431): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0019 | 0/0 | 2422 | 4 | 1 | 1 | 1 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2417): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0020 | 0/0 | 2422 | 4 | 4 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2417): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0021 | 0/0 | 2425 | 4 | 3 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2420): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0022 | 0/0 | 2422 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2417): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0023 | 0/0 | 2426 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2421): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0024 | 0/0 | 2430 | 3 | 2 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2425): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0025 | 0/0 | 2432 | 3 | 2 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2427): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0026 | 0/0 | 2424 | 2 | 1 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2419): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0027 | 0/0 | 2426 | 2 | 0 | 1 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2421): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0028 | 0/0 | 2425 | 2 | 0 | 1 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2420): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0029 | 0/0 | 2435 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2430): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0030 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2409): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0031 | 0/0 | 2416 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2411): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0032 | 0/0 | 2413 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2408): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0033 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2416): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0034 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2416): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0035 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2423): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0036 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2423): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0037 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2425): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0038 | 0/0 | 2425 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2420): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0039 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2427): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0040 | 0/0 | 2434 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2429): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0041 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2432): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0042 | 0/0 | 2439 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2434): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0043 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2427): Show |
chr2 | 17535696 | 17662018 |
a0001c0001t0044 | 0/0 | 2428 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | AATCT others(2423): Show |
chr2 | 17535696 | 17662018 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0005g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0011g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0014g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0014g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0014g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0014g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0015g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0015g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0015g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0015g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0016g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0016g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0016g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0017g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0017g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0017g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0018g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0018g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0018g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0019g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0019g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0019g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0019g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0020g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0020g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0021g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0021g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0021g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0021g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0022g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0022g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0023g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0023g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0023g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0024g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0024g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0024g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0025g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0025g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0025g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0026g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0026g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0027g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0027g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0028g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0028g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0029g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0029g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0030g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0031g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0032g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0033g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0034g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0035g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0036g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0037g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0038g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0039g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0040g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0041g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0042g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0043g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
a0001c0001t0044g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0055 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00140 | hp1 | a0001 | c0001 | t0027 | g0029 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00140 | hp2 | a0001 | c0001 | t0015 | g0108 | EUR | GBR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0024 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0050 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00323 | hp2 | a0001 | c0001 | t0013 | g0069 | EUR | FIN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | CHS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0190 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0163 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0031 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00741 | hp1 | a0001 | c0001 | t0015 | g0019 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01069 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0187 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01070 | hp2 | a0001 | c0001 | t0011 | g0102 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0189 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01099 | hp1 | a0001 | c0001 | t0014 | g0214 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0115 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01175 | hp1 | a0001 | c0001 | t0009 | g0082 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01175 | hp2 | a0001 | c0001 | t0027 | g0018 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01192 | hp1 | a0001 | c0001 | t0013 | g0073 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01243 | hp1 | a0001 | c0001 | t0042 | g0210 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01243 | hp2 | a0001 | c0001 | t0015 | g0044 | AMR | PUR | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01256 | hp1 | a0001 | c0001 | t0013 | g0072 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01256 | hp2 | a0001 | c0001 | t0019 | g0160 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01257 | hp1 | a0001 | c0001 | t0013 | g0094 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0028 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01258 | hp1 | a0001 | c0001 | t0013 | g0071 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0196 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01358 | hp2 | a0001 | c0001 | t0013 | g0068 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01433 | hp1 | a0001 | c0001 | t0014 | g0088 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01433 | hp2 | a0001 | c0001 | t0011 | g0109 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01496 | hp1 | a0001 | c0001 | t0034 | g0107 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0084 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0020 | EUR | IBS | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0080 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01934 | hp2 | a0001 | c0001 | t0021 | g0191 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01981 | hp1 | a0001 | c0001 | t0028 | g0035 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0177 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02145 | hp2 | a0001 | c0001 | t0038 | g0197 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02155 | hp1 | a0001 | c0001 | t0019 | g0045 | EAS | CDX | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CDX | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02257 | hp1 | a0001 | c0001 | t0020 | g0200 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02258 | hp1 | a0001 | c0001 | t0017 | g0213 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0117 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02451 | hp1 | a0001 | c0001 | t0025 | g0151 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02451 | hp2 | a0001 | c0001 | t0041 | g0209 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0126 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02602 | hp1 | a0001 | c0001 | t0015 | g0026 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02602 | hp2 | a0001 | c0001 | t0028 | g0015 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02615 | hp1 | a0001 | c0001 | t0030 | g0131 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02615 | hp2 | a0001 | c0001 | t0023 | g0083 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0128 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02630 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0133 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0079 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02723 | hp2 | a0001 | c0001 | t0037 | g0127 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0157 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0129 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02886 | hp2 | a0001 | c0001 | t0040 | g0125 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02896 | hp2 | a0001 | c0001 | t0024 | g0164 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02897 | hp2 | a0001 | c0001 | t0024 | g0165 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02922 | hp1 | a0001 | c0001 | t0017 | g0013 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02922 | hp2 | a0001 | c0001 | t0029 | g0211 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02965 | hp1 | a0001 | c0001 | t0036 | g0003 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02965 | hp2 | a0001 | c0001 | t0022 | g0009 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03041 | hp2 | a0001 | c0001 | t0035 | g0218 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0167 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0105 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03130 | hp1 | a0001 | c0001 | t0017 | g0065 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03130 | hp2 | a0001 | c0001 | t0029 | g0208 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03195 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0116 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0077 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03239 | hp2 | a0001 | c0001 | t0011 | g0098 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0114 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0011 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03516 | hp1 | a0001 | c0001 | t0021 | g0091 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0066 | AFR | GWD | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03579 | hp2 | a0001 | c0001 | t0019 | g0195 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03654 | hp1 | a0001 | c0001 | t0039 | g0101 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03654 | hp2 | a0001 | c0001 | t0019 | g0062 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0154 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03669 | hp2 | a0001 | c0001 | t0012 | g0142 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03688 | hp1 | a0001 | c0001 | t0012 | g0134 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03710 | hp2 | a0001 | c0001 | t0011 | g0092 | SAS | PJL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG04204 | hp1 | a0001 | c0001 | t0009 | g0155 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG04204 | hp2 | a0001 | c0001 | t0031 | g0156 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0188 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG04228 | hp2 | a0001 | c0001 | t0014 | g0093 | SAS | STU | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18612 | hp2 | a0001 | c0001 | t0012 | g0182 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18906 | hp1 | a0001 | c0001 | t0022 | g0009 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18942 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18945 | hp2 | a0001 | c0001 | t0024 | g0162 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18948 | hp1 | a0001 | c0001 | t0044 | g0186 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18977 | hp1 | a0001 | c0001 | t0018 | g0179 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18977 | hp2 | a0001 | c0001 | t0016 | g0041 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18980 | hp2 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18983 | hp1 | a0001 | c0001 | t0043 | g0033 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18983 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18993 | hp1 | a0001 | c0001 | t0016 | g0153 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0185 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19011 | hp2 | a0001 | c0001 | t0012 | g0180 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19030 | hp2 | a0001 | c0001 | t0022 | g0118 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19043 | hp1 | a0001 | c0001 | t0025 | g0166 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19043 | hp2 | a0001 | c0001 | t0026 | g0193 | AFR | LWK | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19055 | hp1 | a0001 | c0001 | t0018 | g0057 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19055 | hp2 | a0001 | c0001 | t0018 | g0184 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19064 | hp1 | a0001 | c0001 | t0025 | g0040 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19064 | hp2 | a0001 | c0001 | t0012 | g0183 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19067 | hp2 | a0001 | c0001 | t0014 | g0081 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19070 | hp2 | a0001 | c0001 | t0016 | g0161 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19077 | hp2 | a0001 | c0001 | t0015 | g0152 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | YRI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0113 | AFR | ASW | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | ASW | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20752 | hp1 | a0001 | c0001 | t0026 | g0194 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0042 | EUR | TSI | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20905 | hp1 | a0001 | c0001 | t0032 | g0207 | SAS | GIH | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA20905 | hp2 | a0001 | c0001 | t0012 | g0144 | SAS | GIH | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0202 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02109 | hp2 | a0001 | c0001 | t0021 | g0090 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02486 | hp1 | a0001 | c0001 | t0021 | g0192 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02559 | hp1 | a0001 | c0001 | t0023 | g0132 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03471 | hp1 | a0001 | c0001 | t0033 | g0199 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18955 | hp1 | a0001 | c0001 | t0014 | g0100 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0067 | REF | REF | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0215 | REF | REF | VSNL1_chr2_17535696_17662018 | VSNL1 | chr2 | 17535696 | 17662018 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17540852 | T | C | 1 | a0001c0001t0026 | 2 | NA19043.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-72T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/4 | 51223 | chr2 | 17540852 | ||||||
chr2:17655455 | T | TCA | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0021 others(3): Show |
29 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*107dupCA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | T | TCACA | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(4): Show |
51 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*107dupCACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | T | TCACACA | 3 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0040 |
14 | HG01099.hp1 HG01433.hp1 HG02886.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*102_*107dupCACACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | T | TCACACAC others(1): Show |
2 | a0001c0001t0013 a0001c0001t0018 |
11 | HG00323.hp2 HG01192.hp1 HG01256.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*107dupCACACA others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | T | TCACACAC others(5): Show |
1 | a0001c0001t0029 | 2 | HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*96_*107dupCACACAC others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | T | TCACACAC others(7): Show |
1 | a0001c0001t0041 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94_*107dupCACACAC others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | T | TCACACAC others(9): Show |
1 | a0001c0001t0042 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92_*107dupCACACAC others(9): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCA | T | 5 | a0001c0001t0015 a0001c0001t0023 a0001c0001t0027 others(2): Show |
12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*107delCA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 106 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCACA | T | 3 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0026 |
50 | HG00408.hp2 HG00438.hp1 HG00735.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*107delCACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 104 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCACACA | T | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0022 |
11 | HG01256.hp2 HG02155.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*102_*107delCACACA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 102 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCACACAC others(1): Show |
T | 1 | a0001c0001t0010 | 7 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*107delCACACA others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 100 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0032 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98_*107delCACACAC others(3): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 98 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0031 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96_*107delCACACAC others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 96 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655455 | TCACACAC others(7): Show |
T | 1 | a0001c0001t0030 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94_*107delCACACAC others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 94 | INFO_REALIGN_3_PRIME | chr2 | 17655455 | |||||
chr2:17655498 | CACA | C | 1 | a0001c0001t0028 | 2 | HG01981.hp1 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*106_*108delCAA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 106 | INFO_REALIGN_3_PRIME | chr2 | 17655498 | |||||
chr2:17655501 | A | ACACACAC others(4): Show |
1 | a0001c0001t0005 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107_*108insCACACA others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | chr2 | 17655501 | ||||||
chr2:17655502 | A | C | 2 | a0001c0001t0043 a0001c0001t0044 |
2 | NA18948.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*108A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 108 | chr2 | 17655502 | ||||||
chr2:17655570 | T | G | 1 | a0001c0001t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 176 | chr2 | 17655570 | ||||||
chr2:17655815 | T | A | 1 | a0001c0001t0039 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 421 | chr2 | 17655815 | ||||||
chr2:17656392 | C | T | 1 | a0001c0001t0034 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 998 | chr2 | 17656392 | ||||||
chr2:17656474 | C | T | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(5): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1080C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1080 | chr2 | 17656474 | ||||||
chr2:17656598 | TAACAG | T | 10 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0021 others(7): Show |
28 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1217delAGAA others(1): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1213 | INFO_REALIGN_3_PRIME | chr2 | 17656598 | |||||
chr2:17656725 | A | G | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(17): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1331A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1331 | chr2 | 17656725 | ||||||
chr2:17656755 | G | A | 3 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0025 |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1361G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1361 | chr2 | 17656755 | ||||||
chr2:17656869 | C | A | 1 | a0001c0001t0020 | 4 | HG02257.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1475C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1475 | chr2 | 17656869 | ||||||
chr2:17656906 | G | C | 1 | a0001c0001t0038 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1512G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 4/4 | 1512 | chr2 | 17656906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17541155 | G | GTC | 4 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0023g0011 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+239_-6+240dupCT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17541155 | ||||||
chr2:17541330 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-6+412T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541330 | |||||||
chr2:17541367 | G | A | 1 | a0001c0001t0017g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6+449G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541367 | |||||||
chr2:17541387 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+469G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541387 | |||||||
chr2:17541430 | C | A | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-6+512C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541430 | |||||||
chr2:17541461 | C | A | 11 | a0001c0001t0004g0201 a0001c0001t0007g0196 a0001c0001t0007g0198 others(8): Show |
11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+543C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541461 | |||||||
chr2:17541530 | GA | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+616delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17541530 | ||||||
chr2:17541917 | G | A | 6 | a0001c0001t0006g0070 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG00323.hp2 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+999G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17541917 | |||||||
chr2:17542068 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+1150A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542068 | |||||||
chr2:17542094 | A | G | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+1176A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542094 | |||||||
chr2:17542205 | TTG | T | 45 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(42): Show |
46 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-6+1298_-6+1299del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17542205 | ||||||
chr2:17542292 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+1374A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542292 | |||||||
chr2:17542297 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-6+1379A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542297 | |||||||
chr2:17542418 | G | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+1500G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542418 | |||||||
chr2:17542663 | T | C | 1 | a0001c0001t0004g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-6+1745T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542663 | |||||||
chr2:17542679 | G | T | 2 | a0001c0001t0011g0189 a0001c0001t0011g0190 |
2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-6+1761G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542679 | |||||||
chr2:17542726 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+1808A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542726 | |||||||
chr2:17542791 | T | C | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-6+1873T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542791 | |||||||
chr2:17542831 | G | T | 1 | a0001c0001t0012g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-6+1913G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17542831 | |||||||
chr2:17543196 | G | C | 1 | a0001c0001t0013g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-6+2278G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17543196 | |||||||
chr2:17543633 | G | T | 1 | a0001c0001t0007g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-6+2715G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17543633 | |||||||
chr2:17543930 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+3012T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17543930 | |||||||
chr2:17544008 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-6+3090A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544008 | |||||||
chr2:17544419 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-6+3501G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544419 | |||||||
chr2:17544668 | A | G | 10 | a0001c0001t0005g0181 a0001c0001t0009g0178 a0001c0001t0009g0185 others(7): Show |
11 | HG00408.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6+3750A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544668 | |||||||
chr2:17544800 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+3882G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544800 | |||||||
chr2:17544835 | T | C | 7 | a0001c0001t0003g0007 a0001c0001t0008g0003 a0001c0001t0008g0012 others(4): Show |
8 | HG01109.hp2 HG02717.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+3917T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544835 | |||||||
chr2:17544960 | C | T | 1 | a0001c0001t0010g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-6+4042C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17544960 | |||||||
chr2:17545032 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-6+4114C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545032 | |||||||
chr2:17545243 | C | G | 2 | a0001c0001t0026g0193 a0001c0001t0026g0194 |
2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+4325C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545243 | |||||||
chr2:17545343 | T | G | 1 | a0001c0001t0010g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-6+4425T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545343 | |||||||
chr2:17545851 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+4933T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545851 | |||||||
chr2:17545942 | G | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+5024G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17545942 | |||||||
chr2:17546242 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-6+5324C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17546242 | |||||||
chr2:17546412 | G | GT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+5502dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17546412 | ||||||
chr2:17546817 | G | A | 1 | a0001c0001t0011g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6+5899G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17546817 | |||||||
chr2:17546933 | AT | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+6016delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17546933 | |||||||
chr2:17547187 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-6+6269G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547187 | |||||||
chr2:17547435 | A | G | 1 | a0001c0001t0007g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6+6517A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547435 | |||||||
chr2:17547704 | T | C | 1 | a0001c0001t0028g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6+6786T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547704 | |||||||
chr2:17547929 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-6+7011G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17547929 | |||||||
chr2:17548019 | T | G | 3 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 |
3 | HG02559.hp2 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-6+7101T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548019 | |||||||
chr2:17548048 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-6+7130C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548048 | |||||||
chr2:17548056 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+7138C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548056 | |||||||
chr2:17548562 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-6+7644T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548562 | |||||||
chr2:17548948 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8030T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548948 | |||||||
chr2:17548952 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-6+8034T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17548952 | |||||||
chr2:17549130 | T | C | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+8212T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549130 | |||||||
chr2:17549162 | T | C | 17 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(14): Show |
17 | HG00639.hp1 HG01074.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6+8244T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549162 | |||||||
chr2:17549172 | C | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8254C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549172 | |||||||
chr2:17549490 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8572C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549490 | |||||||
chr2:17549631 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+8713C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549631 | |||||||
chr2:17549686 | A | C | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+8768A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549686 | |||||||
chr2:17549897 | G | A | 1 | a0001c0001t0012g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6+8979G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17549897 | |||||||
chr2:17550067 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-6+9149C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550067 | |||||||
chr2:17550383 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+9465A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550383 | |||||||
chr2:17550392 | G | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 |
3 | HG00741.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-6+9474G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550392 | |||||||
chr2:17550501 | G | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+9583G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550501 | |||||||
chr2:17550843 | T | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+9925T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550843 | |||||||
chr2:17550910 | T | C | 3 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+9992T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17550910 | |||||||
chr2:17551156 | G | C | 7 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(4): Show |
7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+10238G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551156 | |||||||
chr2:17551236 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+10318A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551236 | |||||||
chr2:17551763 | A | G | 1 | a0001c0001t0005g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-6+10845A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551763 | |||||||
chr2:17551896 | T | TA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(55): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-6+10998dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17551896 | ||||||
chr2:17551896 | T | TAA | 5 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(2): Show |
5 | HG00741.hp2 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6+10997_-6+10998d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17551896 | ||||||
chr2:17551896 | TA | T | 13 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(10): Show |
16 | HG00639.hp1 HG01074.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-6+10998delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17551896 | ||||||
chr2:17551918 | C | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11000C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551918 | |||||||
chr2:17551926 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11008T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551926 | |||||||
chr2:17551970 | G | A | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6+11052G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17551970 | |||||||
chr2:17552043 | C | CA | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-6+11132dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17552043 | ||||||
chr2:17552092 | C | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11174C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552092 | |||||||
chr2:17552199 | C | CA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-6+11294dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17552199 | ||||||
chr2:17552199 | C | CAA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0004g0020 others(3): Show |
6 | HG00741.hp1 HG01123.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+11293_-6+11294d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17552199 | ||||||
chr2:17552213 | C | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+11295C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552213 | |||||||
chr2:17552243 | G | T | 1 | a0001c0001t0006g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-6+11325G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552243 | |||||||
chr2:17552307 | T | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+11389T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552307 | |||||||
chr2:17552523 | C | T | 4 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(1): Show |
6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+11605C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552523 | |||||||
chr2:17552588 | C | G | 2 | a0001c0001t0004g0020 a0001c0001t0004g0032 |
2 | HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-6+11670C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552588 | |||||||
chr2:17552661 | T | C | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+11743T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552661 | |||||||
chr2:17552661 | T | G | 1 | a0001c0001t0009g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-6+11743T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552661 | |||||||
chr2:17552831 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-6+11913A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552831 | |||||||
chr2:17552950 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-6+12032C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552950 | |||||||
chr2:17552969 | A | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12051A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17552969 | |||||||
chr2:17553033 | G | A | 1 | a0001c0001t0023g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-6+12115G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553033 | |||||||
chr2:17553040 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12122C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553040 | |||||||
chr2:17553054 | G | C | 1 | a0001c0001t0028g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-6+12136G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553054 | |||||||
chr2:17553333 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12415T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553333 | |||||||
chr2:17553465 | A | T | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0158 others(44): Show |
49 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-6+12547A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553465 | |||||||
chr2:17553531 | T | C | 2 | a0001c0001t0011g0189 a0001c0001t0011g0190 |
2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-6+12613T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553531 | |||||||
chr2:17553769 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12851G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553769 | |||||||
chr2:17553775 | CACGA | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12859_-6+12862d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17553775 | ||||||
chr2:17553777 | C | T | 1 | a0001c0001t0008g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+12859C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553777 | |||||||
chr2:17553815 | T | A | 7 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6+12897T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553815 | |||||||
chr2:17553916 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+12998C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17553916 | |||||||
chr2:17554054 | G | A | 45 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(42): Show |
46 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-6+13136G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554054 | |||||||
chr2:17554148 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-6+13230G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554148 | |||||||
chr2:17554166 | A | C | 1 | a0001c0001t0012g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6+13248A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554166 | |||||||
chr2:17554263 | A | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13345A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554263 | |||||||
chr2:17554493 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13575C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554493 | |||||||
chr2:17554561 | T | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13643T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554561 | |||||||
chr2:17554575 | C | T | 1 | a0001c0001t0012g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-6+13657C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554575 | |||||||
chr2:17554583 | T | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+13665T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554583 | |||||||
chr2:17554594 | A | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+13676A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554594 | |||||||
chr2:17554687 | A | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+13769A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554687 | |||||||
chr2:17554737 | C | T | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+13819C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554737 | |||||||
chr2:17554827 | A | G | 1 | a0001c0001t0014g0214 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+13909A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17554827 | |||||||
chr2:17555019 | T | TTTTAAAA others(10): Show |
3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 |
3 | HG00280.hp1 HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-6+14109_-6+14110i others(19): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17555019 | ||||||
chr2:17555186 | A | G | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+14268A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555186 | |||||||
chr2:17555416 | C | T | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+14498C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555416 | |||||||
chr2:17555454 | A | G | 1 | a0001c0001t0009g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-6+14536A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555454 | |||||||
chr2:17555682 | A | G | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+14764A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555682 | |||||||
chr2:17555689 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+14771C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555689 | |||||||
chr2:17555763 | T | G | 1 | a0001c0001t0011g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6+14845T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555763 | |||||||
chr2:17555873 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+14955G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555873 | |||||||
chr2:17555895 | T | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+14977T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555895 | |||||||
chr2:17555946 | A | G | 1 | a0001c0001t0007g0006 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-6+15028A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555946 | |||||||
chr2:17555997 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15079C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17555997 | |||||||
chr2:17556246 | T | C | 1 | a0001c0001t0010g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-6+15328T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556246 | |||||||
chr2:17556304 | A | G | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+15386A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556304 | |||||||
chr2:17556495 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-6+15577T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556495 | |||||||
chr2:17556630 | A | C | 2 | a0001c0001t0026g0193 a0001c0001t0026g0194 |
2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15712A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556630 | |||||||
chr2:17556649 | G | A | 1 | a0001c0001t0043g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-6+15731G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556649 | |||||||
chr2:17556684 | T | C | 1 | a0001c0001t0006g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-6+15766T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556684 | |||||||
chr2:17556697 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15779G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556697 | |||||||
chr2:17556724 | G | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+15806G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556724 | |||||||
chr2:17556766 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15848T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556766 | |||||||
chr2:17556767 | A | T | 1 | a0001c0001t0001g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15849A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556767 | |||||||
chr2:17556768 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15850C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556768 | |||||||
chr2:17556769 | C | A | 1 | a0001c0001t0001g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6+15851C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556769 | |||||||
chr2:17556932 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+16014C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556932 | |||||||
chr2:17556952 | A | G | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-6+16034A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17556952 | |||||||
chr2:17557096 | C | T | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+16178C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557096 | |||||||
chr2:17557275 | A | G | 2 | a0001c0001t0026g0193 a0001c0001t0026g0194 |
2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16357A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557275 | |||||||
chr2:17557399 | T | C | 6 | a0001c0001t0003g0084 a0001c0001t0003g0085 a0001c0001t0003g0086 others(3): Show |
6 | HG00735.hp1 HG01433.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+16481T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557399 | |||||||
chr2:17557487 | A | G | 46 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(43): Show |
47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-6+16569A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557487 | |||||||
chr2:17557507 | T | C | 1 | a0001c0001t0009g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-6+16589T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557507 | |||||||
chr2:17557524 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16606A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557524 | |||||||
chr2:17557654 | C | T | 2 | a0001c0001t0026g0193 a0001c0001t0026g0194 |
2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16736C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557654 | |||||||
chr2:17557841 | A | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16923A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557841 | |||||||
chr2:17557864 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+16946C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17557864 | |||||||
chr2:17558071 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17153G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558071 | |||||||
chr2:17558091 | C | T | 1 | a0001c0001t0011g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-6+17173C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558091 | |||||||
chr2:17558160 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17242C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558160 | |||||||
chr2:17558326 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6+17408G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558326 | |||||||
chr2:17558571 | G | A | 1 | a0001c0001t0026g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-6+17653G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558571 | |||||||
chr2:17558576 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17658T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558576 | |||||||
chr2:17558596 | A | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17678A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558596 | |||||||
chr2:17558627 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+17709C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17558627 | |||||||
chr2:17559109 | G | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+18191G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559109 | |||||||
chr2:17559213 | C | A | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-6+18295C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559213 | |||||||
chr2:17559323 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-6+18405G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559323 | |||||||
chr2:17559408 | C | CA | 20 | a0001c0001t0001g0037 a0001c0001t0005g0187 a0001c0001t0006g0002 others(17): Show |
24 | HG01069.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-6+18501dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17559408 | ||||||
chr2:17559419 | AC | A | 13 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0150 others(10): Show |
13 | HG00099.hp2 HG01123.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6+18502delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559419 | |||||||
chr2:17559420 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-6+18502C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559420 | |||||||
chr2:17559683 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6+18765C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559683 | |||||||
chr2:17559789 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+18871A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559789 | |||||||
chr2:17559820 | C | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+18902C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17559820 | |||||||
chr2:17560061 | T | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19143T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560061 | |||||||
chr2:17560126 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-6+19208T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560126 | |||||||
chr2:17560197 | C | CAT | 200 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-6+19289_-6+19290d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17560197 | ||||||
chr2:17560197 | C | CATAT | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19287_-6+19290d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17560197 | ||||||
chr2:17560214 | A | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19296A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560214 | |||||||
chr2:17560233 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-6+19315A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560233 | |||||||
chr2:17560258 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6+19340G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560258 | |||||||
chr2:17560378 | G | A | 1 | a0001c0001t0014g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-6+19460G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560378 | |||||||
chr2:17560580 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-6+19662T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560580 | |||||||
chr2:17560626 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19708T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560626 | |||||||
chr2:17560679 | G | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19761G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560679 | |||||||
chr2:17560719 | A | G | 2 | a0001c0001t0014g0214 a0001c0001t0017g0213 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-6+19801A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560719 | |||||||
chr2:17560730 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+19812G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560730 | |||||||
chr2:17560843 | G | A | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+19925G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560843 | |||||||
chr2:17560937 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20019G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560937 | |||||||
chr2:17560975 | T | C | 2 | a0001c0001t0021g0090 a0001c0001t0021g0091 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6+20057T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17560975 | |||||||
chr2:17561232 | G | T | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20314G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561232 | |||||||
chr2:17561287 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20369T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561287 | |||||||
chr2:17561360 | G | A | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+20442G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561360 | |||||||
chr2:17561836 | T | C | 3 | a0001c0001t0002g0143 a0001c0001t0005g0175 a0001c0001t0012g0142 |
3 | HG00642.hp2 HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-6+20918T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17561836 | |||||||
chr2:17562043 | T | G | 2 | a0001c0001t0016g0161 a0001c0001t0024g0162 |
2 | NA18945.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-6+21125T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562043 | |||||||
chr2:17562068 | T | G | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+21150T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562068 | |||||||
chr2:17562179 | T | C | 3 | a0001c0001t0019g0195 a0001c0001t0026g0193 a0001c0001t0026g0194 |
3 | HG03579.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-6+21261T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562179 | |||||||
chr2:17562268 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-6+21350A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562268 | |||||||
chr2:17562395 | A | C | 1 | a0001c0001t0029g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-6+21477A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562395 | |||||||
chr2:17562545 | A | G | 1 | a0001c0001t0003g0084 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-6+21627A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562545 | |||||||
chr2:17562547 | A | C | 1 | a0001c0001t0034g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-6+21629A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562547 | |||||||
chr2:17562595 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+21677A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562595 | |||||||
chr2:17562648 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+21730A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562648 | |||||||
chr2:17562870 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0015g0019 |
2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-6+21952C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17562870 | |||||||
chr2:17563224 | C | T | 1 | a0001c0001t0014g0214 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+22306C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563224 | |||||||
chr2:17563231 | G | A | 1 | a0001c0001t0011g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-6+22313G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563231 | |||||||
chr2:17563320 | G | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+22402G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563320 | |||||||
chr2:17563394 | T | C | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+22476T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563394 | |||||||
chr2:17563581 | T | G | 2 | a0001c0001t0005g0021 a0001c0001t0028g0015 |
2 | HG00738.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-6+22663T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563581 | |||||||
chr2:17563585 | C | T | 1 | a0001c0001t0017g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6+22667C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563585 | |||||||
chr2:17563679 | G | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+22761G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563679 | |||||||
chr2:17563685 | G | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+22767G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563685 | |||||||
chr2:17563707 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-6+22789C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563707 | |||||||
chr2:17563751 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-6+22833T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563751 | |||||||
chr2:17563789 | GA | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+22878delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17563789 | ||||||
chr2:17563910 | T | C | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6+22992T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17563910 | |||||||
chr2:17564162 | T | G | 2 | a0001c0001t0016g0041 a0001c0001t0025g0040 |
2 | NA18977.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-6+23244T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564162 | |||||||
chr2:17564388 | T | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+23470T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564388 | |||||||
chr2:17564478 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+23560A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564478 | |||||||
chr2:17564574 | G | GT | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+23665dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17564574 | ||||||
chr2:17564643 | C | T | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-6+23725C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17564643 | |||||||
chr2:17565032 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+24114T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565032 | |||||||
chr2:17565071 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 |
3 | HG00280.hp1 HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-6+24153A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565071 | |||||||
chr2:17565169 | A | G | 6 | a0001c0001t0016g0163 a0001c0001t0016g0167 a0001c0001t0024g0164 others(3): Show |
6 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+24251A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565169 | |||||||
chr2:17565402 | C | CA | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+24487dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17565402 | ||||||
chr2:17565617 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+24699A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565617 | |||||||
chr2:17565810 | C | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+24892C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565810 | |||||||
chr2:17565840 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-6+24922T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565840 | |||||||
chr2:17565919 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25001C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17565919 | |||||||
chr2:17566075 | A | G | 1 | a0001c0001t0026g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-6+25157A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566075 | |||||||
chr2:17566163 | T | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25245T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566163 | |||||||
chr2:17566201 | T | C | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-6+25283T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566201 | |||||||
chr2:17566222 | C | G | 1 | a0001c0001t0035g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-6+25304C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566222 | |||||||
chr2:17566284 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6+25366A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566284 | |||||||
chr2:17566301 | T | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25383T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566301 | |||||||
chr2:17566324 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+25406A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566324 | |||||||
chr2:17566599 | A | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-25471A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566599 | |||||||
chr2:17566731 | A | G | 6 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 others(3): Show |
6 | HG01496.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5-25339A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566731 | |||||||
chr2:17566732 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.-5-25338C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566732 | |||||||
chr2:17566787 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-25283C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566787 | |||||||
chr2:17566969 | C | A | 1 | a0001c0001t0017g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5-25101C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17566969 | |||||||
chr2:17567141 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-5-24929T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567141 | |||||||
chr2:17567156 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-5-24914G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567156 | |||||||
chr2:17567275 | C | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24795C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567275 | |||||||
chr2:17567331 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24739A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567331 | |||||||
chr2:17567343 | T | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24727T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567343 | |||||||
chr2:17567353 | C | CT | 47 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0212 others(44): Show |
48 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-5-24693dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | ||||||
chr2:17567353 | C | CTT | 70 | a0001c0001t0002g0121 a0001c0001t0002g0135 a0001c0001t0002g0136 others(67): Show |
73 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-5-24694_-5-24693d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | ||||||
chr2:17567353 | C | CTTT | 19 | a0001c0001t0001g0043 a0001c0001t0002g0122 a0001c0001t0002g0143 others(16): Show |
21 | HG01069.hp2 HG01168.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-5-24695_-5-24693d others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | ||||||
chr2:17567353 | C | CTTTT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5-24696_-5-24693d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | ||||||
chr2:17567353 | C | CTTTTT | 7 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0061 others(4): Show |
7 | HG01175.hp2 HG01934.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-24697_-5-24693d others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | ||||||
chr2:17567353 | CTT | C | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-24694_-5-24693d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17567353 | ||||||
chr2:17567377 | T | A | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-24693T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567377 | |||||||
chr2:17567377 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-24693_-5-24692i others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567377 | |||||||
chr2:17567397 | C | T | 2 | a0001c0001t0027g0018 a0001c0001t0027g0029 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-5-24673C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567397 | |||||||
chr2:17567410 | G | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-24660G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567410 | |||||||
chr2:17567469 | C | G | 36 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(33): Show |
37 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-5-24601C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567469 | |||||||
chr2:17567535 | T | G | 2 | a0001c0001t0014g0214 a0001c0001t0017g0213 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-24535T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567535 | |||||||
chr2:17567561 | T | C | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-24509T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567561 | |||||||
chr2:17567678 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-24392C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567678 | |||||||
chr2:17567682 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-5-24388A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567682 | |||||||
chr2:17567830 | T | C | 1 | a0001c0001t0025g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5-24240T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17567830 | |||||||
chr2:17568158 | T | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-5-23912T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568158 | |||||||
chr2:17568215 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-23855T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568215 | |||||||
chr2:17568382 | C | T | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-23688C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568382 | |||||||
chr2:17568573 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-23497C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568573 | |||||||
chr2:17568592 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-23478C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568592 | |||||||
chr2:17568627 | C | A | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-23443C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17568627 | |||||||
chr2:17569014 | A | C | 53 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(50): Show |
58 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.-5-23056A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569014 | |||||||
chr2:17569223 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22847C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569223 | |||||||
chr2:17569239 | T | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22831T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569239 | |||||||
chr2:17569289 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-5-22781A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569289 | |||||||
chr2:17569294 | G | A | 1 | a0001c0001t0028g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-5-22776G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569294 | |||||||
chr2:17569306 | C | CAA | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22755_-5-22754d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17569306 | ||||||
chr2:17569317 | T | A | 1 | a0001c0001t0004g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-5-22753T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569317 | |||||||
chr2:17569606 | T | G | 7 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-22464T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569606 | |||||||
chr2:17569633 | A | G | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-22437A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569633 | |||||||
chr2:17569650 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-22420A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569650 | |||||||
chr2:17569692 | A | ACTCT | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-22377_-5-22374d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17569692 | ||||||
chr2:17569714 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-5-22356G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569714 | |||||||
chr2:17569880 | C | T | 1 | a0001c0001t0014g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-22190C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17569880 | |||||||
chr2:17570011 | G | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-22059G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570011 | |||||||
chr2:17570184 | G | T | 1 | a0001c0001t0026g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-5-21886G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570184 | |||||||
chr2:17570336 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-5-21734C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570336 | |||||||
chr2:17570366 | G | A | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-21704G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570366 | |||||||
chr2:17570389 | C | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-21681C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570389 | |||||||
chr2:17570861 | A | T | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-21209A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570861 | |||||||
chr2:17570866 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-5-21204G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570866 | |||||||
chr2:17570923 | A | T | 1 | a0001c0001t0010g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-5-21147A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570923 | |||||||
chr2:17570951 | A | T | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-21119A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570951 | |||||||
chr2:17570957 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-21113C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17570957 | |||||||
chr2:17571271 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-5-20799G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571271 | |||||||
chr2:17571314 | G | T | 1 | a0001c0001t0017g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-20756G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571314 | |||||||
chr2:17571354 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-20716T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571354 | |||||||
chr2:17571546 | C | T | 5 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-20524C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571546 | |||||||
chr2:17571585 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20485A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571585 | |||||||
chr2:17571588 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20482A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571588 | |||||||
chr2:17571589 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20481A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571589 | |||||||
chr2:17571590 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20480A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571590 | |||||||
chr2:17571592 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20478A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571592 | |||||||
chr2:17571596 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20474A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571596 | |||||||
chr2:17571601 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20469G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571601 | |||||||
chr2:17571602 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20468C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571602 | |||||||
chr2:17571604 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20466C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571604 | |||||||
chr2:17571605 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20465C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571605 | |||||||
chr2:17571606 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20464T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571606 | |||||||
chr2:17571608 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20462C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571608 | |||||||
chr2:17571609 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20461T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571609 | |||||||
chr2:17571613 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20457C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571613 | |||||||
chr2:17571615 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20455C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571615 | |||||||
chr2:17571616 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20454C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571616 | |||||||
chr2:17571617 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20453A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571617 | |||||||
chr2:17571619 | G | C | 1 | a0001c0001t0002g0039 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-5-20451G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571619 | |||||||
chr2:17571620 | G | C | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20450G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571620 | |||||||
chr2:17571622 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20448C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571622 | |||||||
chr2:17571624 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20446A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571624 | |||||||
chr2:17571625 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20445T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571625 | |||||||
chr2:17571627 | C | T | 3 | a0001c0001t0002g0038 a0001c0001t0009g0185 a0001c0001t0044g0186 |
3 | HG02129.hp2 NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-5-20443C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571627 | |||||||
chr2:17571629 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20441A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571629 | |||||||
chr2:17571631 | G | C | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20439G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571631 | |||||||
chr2:17571634 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20436C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571634 | |||||||
chr2:17571637 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20433A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571637 | |||||||
chr2:17571638 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20432G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571638 | |||||||
chr2:17571647 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20423C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571647 | |||||||
chr2:17571652 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20418C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571652 | |||||||
chr2:17571654 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20416G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571654 | |||||||
chr2:17571655 | ACCAGGTT others(4): Show |
A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20412_-5-20402d others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17571655 | ||||||
chr2:17571667 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20403C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571667 | |||||||
chr2:17571668 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20402C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571668 | |||||||
chr2:17571672 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20398T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571672 | |||||||
chr2:17571673 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20397T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571673 | |||||||
chr2:17571674 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20396G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571674 | |||||||
chr2:17571682 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20388C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571682 | |||||||
chr2:17571686 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20384C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571686 | |||||||
chr2:17571687 | T | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20383T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571687 | |||||||
chr2:17571689 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20381G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571689 | |||||||
chr2:17571695 | G | GAACTGCT others(4): Show |
1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20375_-5-20374i others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571695 | |||||||
chr2:17571699 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20371A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571699 | |||||||
chr2:17571704 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20366C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571704 | |||||||
chr2:17571706 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20364A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571706 | |||||||
chr2:17571710 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-20360A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571710 | |||||||
chr2:17571740 | T | A | 1 | a0001c0001t0015g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5-20330T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17571740 | |||||||
chr2:17572035 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-20035A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572035 | |||||||
chr2:17572045 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-20025C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572045 | |||||||
chr2:17572063 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0019g0160 |
2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-5-20007C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572063 | |||||||
chr2:17572064 | G | T | 2 | a0001c0001t0014g0214 a0001c0001t0017g0213 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-20006G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572064 | |||||||
chr2:17572099 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-19971T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572099 | |||||||
chr2:17572383 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-5-19687G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572383 | |||||||
chr2:17572404 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5-19666A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572404 | |||||||
chr2:17572569 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-19501C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17572569 | |||||||
chr2:17572886 | TTTGA | T | 31 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(28): Show |
34 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-19180_-5-19177d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17572886 | ||||||
chr2:17573040 | T | C | 22 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0150 others(19): Show |
23 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-19030T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573040 | |||||||
chr2:17573049 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-5-19021A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573049 | |||||||
chr2:17573128 | T | C | 2 | a0001c0001t0014g0214 a0001c0001t0017g0213 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-5-18942T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573128 | |||||||
chr2:17573131 | G | A | 1 | a0001c0001t0007g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-5-18939G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573131 | |||||||
chr2:17573339 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5-18731G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573339 | |||||||
chr2:17573453 | C | CA | 32 | a0001c0001t0001g0123 a0001c0001t0001g0168 a0001c0001t0001g0172 others(29): Show |
34 | HG00408.hp1 HG00438.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5-18604dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17573453 | ||||||
chr2:17573502 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-18568A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573502 | |||||||
chr2:17573510 | G | A | 22 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0150 others(19): Show |
23 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-18560G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573510 | |||||||
chr2:17573965 | T | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-18105T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573965 | |||||||
chr2:17573990 | C | G | 1 | a0001c0001t0017g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-18080C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17573990 | |||||||
chr2:17574162 | C | T | 1 | a0001c0001t0043g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-5-17908C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574162 | |||||||
chr2:17574172 | G | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17898G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574172 | |||||||
chr2:17574202 | T | TC | 25 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(22): Show |
26 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.-5-17860dupC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17574202 | ||||||
chr2:17574332 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17738A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574332 | |||||||
chr2:17574445 | G | A | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-17625G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574445 | |||||||
chr2:17574451 | C | A | 18 | a0001c0001t0004g0173 a0001c0001t0008g0128 a0001c0001t0008g0129 others(15): Show |
18 | HG00639.hp1 HG01074.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5-17619C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574451 | |||||||
chr2:17574471 | ATCTT | A | 7 | a0001c0001t0003g0007 a0001c0001t0008g0003 a0001c0001t0008g0012 others(4): Show |
8 | HG01109.hp2 HG02717.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-17594_-5-17591d others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17574471 | ||||||
chr2:17574492 | G | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17578G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574492 | |||||||
chr2:17574494 | TA | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17574delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17574494 | ||||||
chr2:17574699 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-5-17371C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574699 | |||||||
chr2:17574769 | T | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17301T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574769 | |||||||
chr2:17574803 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-17267G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574803 | |||||||
chr2:17574832 | T | A | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-17238T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574832 | |||||||
chr2:17574911 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-5-17159C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574911 | |||||||
chr2:17574917 | C | A | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-17153C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574917 | |||||||
chr2:17574999 | A | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-17071A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17574999 | |||||||
chr2:17575044 | G | C | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-17026G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575044 | |||||||
chr2:17575116 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.-5-16954C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575116 | |||||||
chr2:17575127 | C | A | 22 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0150 others(19): Show |
23 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-16943C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575127 | |||||||
chr2:17575129 | A | G | 20 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0135 others(17): Show |
20 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-5-16941A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575129 | |||||||
chr2:17575132 | A | G | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-16938A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575132 | |||||||
chr2:17575174 | C | A | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-16896C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575174 | |||||||
chr2:17575309 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-5-16761T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575309 | |||||||
chr2:17575339 | T | A | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-16731T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575339 | |||||||
chr2:17575534 | T | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16536T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575534 | |||||||
chr2:17575564 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16506C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575564 | |||||||
chr2:17575629 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16441A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575629 | |||||||
chr2:17575659 | C | T | 1 | a0001c0001t0010g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-5-16411C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575659 | |||||||
chr2:17575696 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-5-16374C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575696 | |||||||
chr2:17575697 | G | A | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-16373G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575697 | |||||||
chr2:17575771 | G | A | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-16299G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575771 | |||||||
chr2:17575824 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16246T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575824 | |||||||
chr2:17575955 | A | G | 8 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0150 others(5): Show |
8 | HG00099.hp2 HG01123.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-16115A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17575955 | |||||||
chr2:17575969 | AT | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-16099delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17575969 | ||||||
chr2:17576126 | C | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15944C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576126 | |||||||
chr2:17576171 | T | C | 2 | a0001c0001t0018g0057 a0001c0001t0019g0045 |
2 | HG02155.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-5-15899T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576171 | |||||||
chr2:17576257 | T | G | 5 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-15813T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576257 | |||||||
chr2:17576531 | G | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15539G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576531 | |||||||
chr2:17576621 | T | C | 1 | a0001c0001t0033g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-5-15449T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576621 | |||||||
chr2:17576840 | C | CTGGTATG others(2): Show |
27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15229_-5-15228i others(11): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17576840 | ||||||
chr2:17576992 | A | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-15078A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17576992 | |||||||
chr2:17577079 | T | C | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-14991T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577079 | |||||||
chr2:17577177 | C | T | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-14893C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577177 | |||||||
chr2:17577205 | C | T | 1 | a0001c0001t0009g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5-14865C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577205 | |||||||
chr2:17577476 | A | G | 2 | a0001c0001t0027g0018 a0001c0001t0027g0029 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-5-14594A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577476 | |||||||
chr2:17577736 | A | G | 1 | a0001c0001t0014g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-14334A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577736 | |||||||
chr2:17577792 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-14278T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17577792 | |||||||
chr2:17578002 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-14068T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578002 | |||||||
chr2:17578244 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-5-13826C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578244 | |||||||
chr2:17578432 | G | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-13638G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578432 | |||||||
chr2:17578440 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-5-13630T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578440 | |||||||
chr2:17578498 | C | G | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-13572C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578498 | |||||||
chr2:17578542 | G | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-13528G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578542 | |||||||
chr2:17578854 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5-13216G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578854 | |||||||
chr2:17578901 | A | G | 45 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(42): Show |
46 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-5-13169A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578901 | |||||||
chr2:17578922 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-13148T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17578922 | |||||||
chr2:17579122 | A | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-5-12948A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579122 | |||||||
chr2:17579210 | G | C | 1 | a0001c0001t0015g0019 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-5-12860G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579210 | |||||||
chr2:17579361 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-5-12709C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579361 | |||||||
chr2:17579652 | C | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-12418C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579652 | |||||||
chr2:17579679 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5-12391T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579679 | |||||||
chr2:17579734 | A | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-12336A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17579734 | |||||||
chr2:17580108 | G | A | 11 | a0001c0001t0004g0201 a0001c0001t0007g0196 a0001c0001t0007g0198 others(8): Show |
11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-11962G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580108 | |||||||
chr2:17580225 | G | A | 1 | a0001c0001t0013g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-5-11845G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580225 | |||||||
chr2:17580387 | C | G | 1 | a0001c0001t0012g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-5-11683C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580387 | |||||||
chr2:17580612 | T | G | 1 | a0001c0001t0019g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-5-11458T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580612 | |||||||
chr2:17580618 | A | T | 1 | a0001c0001t0017g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5-11452A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580618 | |||||||
chr2:17580640 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-5-11430C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580640 | |||||||
chr2:17580674 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5-11396C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580674 | |||||||
chr2:17580736 | C | T | 1 | a0001c0001t0006g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-5-11334C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580736 | |||||||
chr2:17580825 | G | A | 1 | a0001c0001t0013g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-5-11245G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580825 | |||||||
chr2:17580997 | C | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-11073C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17580997 | |||||||
chr2:17581185 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
58 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.-5-10885A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581185 | |||||||
chr2:17581518 | T | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-10552T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581518 | |||||||
chr2:17581526 | G | T | 22 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(19): Show |
22 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5-10544G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581526 | |||||||
chr2:17581572 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10498A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581572 | |||||||
chr2:17581765 | TTC | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10299_-5-10298d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17581765 | ||||||
chr2:17581994 | T | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10076T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17581994 | |||||||
chr2:17582015 | T | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-10055T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582015 | |||||||
chr2:17582084 | AC | A | 3 | a0001c0001t0004g0106 a0001c0001t0004g0110 a0001c0001t0017g0080 |
3 | HG01891.hp2 HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-5-9984delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17582084 | ||||||
chr2:17582117 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-9953G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582117 | |||||||
chr2:17582256 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-5-9814G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582256 | |||||||
chr2:17582431 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9639T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582431 | |||||||
chr2:17582435 | A | C | 5 | a0001c0001t0016g0167 a0001c0001t0024g0164 a0001c0001t0024g0165 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-9635A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582435 | |||||||
chr2:17582456 | T | G | 1 | a0001c0001t0004g0024 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-5-9614T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582456 | |||||||
chr2:17582459 | G | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9611G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582459 | |||||||
chr2:17582555 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.-5-9515T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582555 | |||||||
chr2:17582560 | C | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9510C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582560 | |||||||
chr2:17582608 | G | C | 1 | a0001c0001t0032g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-5-9462G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582608 | |||||||
chr2:17582880 | A | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-9190A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582880 | |||||||
chr2:17582971 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-9099C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17582971 | |||||||
chr2:17583084 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-8986T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583084 | |||||||
chr2:17583169 | T | G | 1 | a0001c0001t0011g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-5-8901T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583169 | |||||||
chr2:17583213 | G | A | 1 | a0001c0001t0020g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-5-8857G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583213 | |||||||
chr2:17583330 | T | C | 1 | a0001c0001t0013g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-5-8740T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583330 | |||||||
chr2:17583561 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-8509T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583561 | |||||||
chr2:17583652 | A | G | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-8418A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583652 | |||||||
chr2:17583666 | C | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0016g0153 |
3 | NA18967.hp2 NA18989.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-5-8404C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583666 | |||||||
chr2:17583819 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0032g0207 |
2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-5-8251T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17583819 | |||||||
chr2:17584052 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-5-8018T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584052 | |||||||
chr2:17584076 | T | C | 1 | a0001c0001t0018g0057 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-5-7994T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584076 | |||||||
chr2:17584149 | T | C | 26 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5-7921T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584149 | |||||||
chr2:17584198 | A | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7872A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584198 | |||||||
chr2:17584214 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-5-7856C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584214 | |||||||
chr2:17584250 | AG | A | 22 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(19): Show |
22 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5-7817delG | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17584250 | ||||||
chr2:17584278 | A | G | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-5-7792A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584278 | |||||||
chr2:17584312 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-7758G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584312 | |||||||
chr2:17584370 | G | A | 11 | a0001c0001t0004g0201 a0001c0001t0007g0196 a0001c0001t0007g0198 others(8): Show |
11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5-7700G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584370 | |||||||
chr2:17584794 | C | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7276C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584794 | |||||||
chr2:17584827 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7243T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584827 | |||||||
chr2:17584836 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7234C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584836 | |||||||
chr2:17584838 | TAA | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7231_-5-7230del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584838 | |||||||
chr2:17584841 | C | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7229C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584841 | |||||||
chr2:17584842 | A | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7228A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584842 | |||||||
chr2:17584851 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-5-7219C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584851 | |||||||
chr2:17584875 | C | T | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-7195C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584875 | |||||||
chr2:17584936 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0003g0085 |
2 | HG01981.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-5-7134G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17584936 | |||||||
chr2:17585331 | A | G | 41 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(38): Show |
42 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-5-6739A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585331 | |||||||
chr2:17585382 | T | TA | 45 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(42): Show |
46 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-5-6674dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17585382 | ||||||
chr2:17585382 | TA | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0056 others(7): Show |
10 | HG00099.hp1 HG00639.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5-6674delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17585382 | ||||||
chr2:17585382 | TAA | T | 39 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(36): Show |
40 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-5-6675_-5-6674del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17585382 | ||||||
chr2:17585393 | A | AC | 2 | a0001c0001t0003g0007 a0001c0001t0014g0105 |
3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-5-6677_-5-6676ins others(1): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585393 | |||||||
chr2:17585470 | C | T | 1 | a0001c0001t0009g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5-6600C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585470 | |||||||
chr2:17585639 | T | C | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-6431T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585639 | |||||||
chr2:17585749 | T | C | 56 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(53): Show |
57 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-5-6321T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585749 | |||||||
chr2:17585807 | TC | T | 3 | a0001c0001t0005g0171 a0001c0001t0015g0152 a0001c0001t0017g0066 |
3 | HG02015.hp2 HG03540.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-5-6262delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585807 | |||||||
chr2:17585808 | C | T | 52 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(49): Show |
53 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-5-6262C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585808 | |||||||
chr2:17585826 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5-6244G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17585826 | |||||||
chr2:17586074 | G | T | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-5996G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586074 | |||||||
chr2:17586078 | G | A | 1 | a0001c0001t0034g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-5-5992G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586078 | |||||||
chr2:17586089 | A | T | 1 | a0001c0001t0005g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-5-5981A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586089 | |||||||
chr2:17586341 | G | A | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5729G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586341 | |||||||
chr2:17586405 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-5-5665C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586405 | |||||||
chr2:17586447 | G | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-5623G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586447 | |||||||
chr2:17586493 | C | T | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5577C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586493 | |||||||
chr2:17586610 | C | T | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5460C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586610 | |||||||
chr2:17586666 | AC | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5-5403delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586666 | |||||||
chr2:17586679 | A | T | 1 | a0001c0001t0007g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-5-5391A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586679 | |||||||
chr2:17586714 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-5-5356C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586714 | |||||||
chr2:17586715 | G | A | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-5355G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586715 | |||||||
chr2:17586740 | T | A | 6 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-5330T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586740 | |||||||
chr2:17586748 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-5322C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586748 | |||||||
chr2:17586917 | C | T | 1 | a0001c0001t0017g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-5-5153C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586917 | |||||||
chr2:17586943 | A | G | 1 | a0001c0001t0021g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-5-5127A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586943 | |||||||
chr2:17586995 | G | A | 3 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-5075G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17586995 | |||||||
chr2:17587095 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-5-4975A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587095 | |||||||
chr2:17587109 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-5-4961G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587109 | |||||||
chr2:17587151 | A | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5-4919A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587151 | |||||||
chr2:17587179 | C | T | 1 | a0001c0001t0043g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-5-4891C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587179 | |||||||
chr2:17587296 | A | G | 1 | a0001c0001t0026g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-5-4774A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587296 | |||||||
chr2:17587345 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.-5-4725G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587345 | |||||||
chr2:17587348 | A | AAC | 41 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0159 others(38): Show |
44 | HG00140.hp2 HG00642.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5-4676_-5-4675dup others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | A | AACAC | 13 | a0001c0001t0004g0022 a0001c0001t0004g0096 a0001c0001t0004g0097 others(10): Show |
13 | HG01109.hp2 HG01168.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-4678_-5-4675dup others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | A | AACACAC | 8 | a0001c0001t0001g0017 a0001c0001t0004g0112 a0001c0001t0005g0021 others(5): Show |
8 | HG00738.hp2 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-4680_-5-4675dup others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | A | AACACACA others(3): Show |
1 | a0001c0001t0032g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-5-4684_-5-4675dup others(10): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | A | AACACACA others(5): Show |
1 | a0001c0001t0004g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-5-4686_-5-4675dup others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | AAC | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(54): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.-5-4676_-5-4675del others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | AACAC | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0004g0020 others(10): Show |
13 | HG00438.hp1 HG01243.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.-5-4678_-5-4675del others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | AACACAC | A | 5 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0012g0134 others(2): Show |
5 | HG01981.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5-4680_-5-4675del others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587348 | AACACACA others(7): Show |
A | 1 | a0001c0001t0004g0024 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-5-4688_-5-4675del others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587348 | ||||||
chr2:17587394 | C | CACACACA others(5): Show |
1 | a0001c0001t0016g0161 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-5-4675_-5-4674ins others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | ||||||
chr2:17587394 | C | CACACAT | 5 | a0001c0001t0016g0167 a0001c0001t0024g0164 a0001c0001t0024g0165 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-4675_-5-4674ins others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | ||||||
chr2:17587394 | C | CACAT | 4 | a0001c0001t0016g0153 a0001c0001t0016g0163 a0001c0001t0024g0162 others(1): Show |
4 | HG00639.hp2 NA18945.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-4675_-5-4674ins others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | ||||||
chr2:17587394 | C | CAT | 6 | a0001c0001t0005g0187 a0001c0001t0008g0128 a0001c0001t0009g0178 others(3): Show |
6 | HG01069.hp2 HG01934.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-4671_-5-4670dup others(2): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17587394 | ||||||
chr2:17587394 | C | T | 28 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(25): Show |
29 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.-5-4676C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587394 | |||||||
chr2:17587488 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-4582C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587488 | |||||||
chr2:17587526 | C | G | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4544C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587526 | |||||||
chr2:17587540 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-5-4530C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587540 | |||||||
chr2:17587556 | C | A | 1 | a0001c0001t0034g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-5-4514C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587556 | |||||||
chr2:17587588 | G | C | 10 | a0001c0001t0016g0153 a0001c0001t0016g0161 a0001c0001t0016g0163 others(7): Show |
10 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5-4482G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587588 | |||||||
chr2:17587652 | C | G | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4418C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587652 | |||||||
chr2:17587670 | T | C | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4400T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587670 | |||||||
chr2:17587701 | C | T | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4369C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587701 | |||||||
chr2:17587784 | G | A | 6 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-4286G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587784 | |||||||
chr2:17587811 | A | G | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5-4259A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587811 | |||||||
chr2:17587889 | G | A | 45 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(42): Show |
47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-5-4181G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587889 | |||||||
chr2:17587917 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-4153A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17587917 | |||||||
chr2:17588183 | G | A | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-3887G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588183 | |||||||
chr2:17588408 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-5-3662A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588408 | |||||||
chr2:17588717 | A | T | 52 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(49): Show |
53 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-5-3353A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588717 | |||||||
chr2:17588828 | T | C | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5-3242T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588828 | |||||||
chr2:17588968 | C | T | 1 | a0001c0001t0034g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-5-3102C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588968 | |||||||
chr2:17588971 | T | A | 1 | a0001c0001t0012g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5-3099T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17588971 | |||||||
chr2:17589009 | A | T | 49 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(46): Show |
50 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-5-3061A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589009 | |||||||
chr2:17589030 | A | G | 1 | a0001c0001t0016g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-5-3040A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589030 | |||||||
chr2:17589176 | T | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-5-2894T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589176 | |||||||
chr2:17589305 | G | C | 1 | a0001c0001t0042g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-2765G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589305 | |||||||
chr2:17589315 | A | C | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-5-2755A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589315 | |||||||
chr2:17589385 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-5-2685C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589385 | |||||||
chr2:17589479 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-5-2591C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589479 | |||||||
chr2:17589485 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-2585A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589485 | |||||||
chr2:17589626 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-2444G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589626 | |||||||
chr2:17589670 | T | C | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5-2400T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589670 | |||||||
chr2:17589861 | C | T | 2 | a0001c0001t0027g0018 a0001c0001t0027g0029 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-5-2209C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589861 | |||||||
chr2:17589940 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-2130G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17589940 | |||||||
chr2:17589950 | TTCCTGTT others(5): Show |
T | 45 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(42): Show |
47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-5-2114_-5-2103del others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 17589950 | ||||||
chr2:17590009 | C | T | 18 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0135 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-5-2061C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590009 | |||||||
chr2:17590140 | T | C | 1 | a0001c0001t0023g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5-1930T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590140 | |||||||
chr2:17590146 | T | C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-5-1924T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590146 | |||||||
chr2:17590179 | G | A | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-5-1891G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590179 | |||||||
chr2:17590387 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-5-1683C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590387 | |||||||
chr2:17590829 | G | C | 1 | a0001c0001t0002g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5-1241G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17590829 | |||||||
chr2:17591039 | A | T | 6 | a0001c0001t0007g0198 a0001c0001t0007g0203 a0001c0001t0007g0204 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-1031A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591039 | |||||||
chr2:17591150 | A | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-5-920A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591150 | |||||||
chr2:17591238 | G | T | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0040g0125 |
3 | HG02572.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-5-832G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591238 | |||||||
chr2:17591317 | A | T | 1 | a0001c0001t0006g0002 | 3 | HG02055.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-753A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591317 | |||||||
chr2:17591804 | T | C | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5-266T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591804 | |||||||
chr2:17591978 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0032g0207 |
2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-5-92C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 1/3 | chr2 | 17591978 | |||||||
chr2:17592257 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+21G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592257 | |||||||
chr2:17592361 | T | C | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+125T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592361 | |||||||
chr2:17592489 | T | C | 5 | a0001c0001t0016g0167 a0001c0001t0024g0164 a0001c0001t0024g0165 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+253T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592489 | |||||||
chr2:17592605 | A | AAAAGTAC | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+371_162+377dup others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592605 | ||||||
chr2:17592636 | CTCTCTTT others(10): Show |
C | 1 | a0001c0001t0010g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+402_162+418del others(17): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592636 | ||||||
chr2:17592636 | CTCTCTTT others(11): Show |
C | 1 | a0001c0001t0010g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162+402_162+419del others(18): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592636 | ||||||
chr2:17592640 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0004g0201 a0001c0001t0007g0196 a0001c0001t0020g0200 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+434_162+443dup others(10): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(1): Show |
C | 36 | a0001c0001t0002g0121 a0001c0001t0003g0007 a0001c0001t0003g0074 others(33): Show |
37 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+436_162+443del others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(2): Show |
C | 32 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0122 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+435_162+443del others(9): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0063 others(3): Show |
6 | HG00438.hp1 HG01175.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+434_162+443del others(10): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(4): Show |
C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.162+433_162+443del others(11): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(5): Show |
C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0005g0042 others(25): Show |
28 | HG00323.hp1 HG00639.hp2 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.162+432_162+443del others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0016g0161 a0001c0001t0017g0013 a0001c0001t0017g0065 others(2): Show |
5 | HG02922.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+431_162+443del others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
11 | HG02055.hp2 HG02630.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+430_162+443del others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0020g0117 a0001c0001t0022g0009 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.162+429_162+443del others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+428_162+443del others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+427_162+443del others(17): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(12): Show |
C | 9 | a0001c0001t0005g0181 a0001c0001t0009g0178 a0001c0001t0009g0185 others(6): Show |
10 | HG00408.hp1 NA18612.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+425_162+443del others(19): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592640 | CTTTTTTT others(13): Show |
C | 13 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(10): Show |
13 | HG00438.hp2 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.162+424_162+443del others(20): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17592640 | ||||||
chr2:17592642 | T | C | 1 | a0001c0001t0006g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162+406T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592642 | |||||||
chr2:17592648 | T | C | 1 | a0001c0001t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162+412T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592648 | |||||||
chr2:17592649 | T | C | 4 | a0001c0001t0003g0085 a0001c0001t0003g0086 a0001c0001t0014g0105 others(1): Show |
4 | HG01981.hp2 HG02004.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+413T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592649 | |||||||
chr2:17592650 | T | C | 30 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(27): Show |
31 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.162+414T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592650 | |||||||
chr2:17592651 | T | C | 10 | a0001c0001t0003g0099 a0001c0001t0004g0097 a0001c0001t0004g0104 others(7): Show |
10 | HG01069.hp1 HG01070.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+415T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592651 | |||||||
chr2:17592652 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.162+416T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592652 | |||||||
chr2:17592653 | T | C | 2 | a0001c0001t0005g0187 a0001c0001t0016g0041 |
2 | HG01069.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.162+417T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592653 | |||||||
chr2:17592654 | T | C | 18 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(15): Show |
18 | HG00639.hp2 HG01934.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.162+418T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592654 | |||||||
chr2:17592655 | T | C | 4 | a0001c0001t0016g0161 a0001c0001t0017g0065 a0001c0001t0017g0066 others(1): Show |
4 | HG03130.hp1 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+419T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592655 | |||||||
chr2:17592659 | T | C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+423T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592659 | |||||||
chr2:17592661 | T | C | 9 | a0001c0001t0005g0181 a0001c0001t0009g0178 a0001c0001t0009g0185 others(6): Show |
10 | HG00408.hp1 NA18612.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+425T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592661 | |||||||
chr2:17592662 | T | C | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(9): Show |
12 | HG00438.hp2 HG02015.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+426T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592662 | |||||||
chr2:17592731 | A | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+495A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592731 | |||||||
chr2:17592879 | C | T | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+643C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592879 | |||||||
chr2:17592886 | G | A | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+650G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592886 | |||||||
chr2:17592967 | C | A | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+731C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17592967 | |||||||
chr2:17593154 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+918G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593154 | |||||||
chr2:17593239 | T | C | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+1003T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593239 | |||||||
chr2:17593367 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+1131A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593367 | |||||||
chr2:17593379 | T | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1143T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593379 | |||||||
chr2:17593418 | G | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1182G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593418 | |||||||
chr2:17593434 | T | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1198T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593434 | |||||||
chr2:17593479 | A | G | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1243A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593479 | |||||||
chr2:17593551 | T | C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+1315T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593551 | |||||||
chr2:17593566 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.162+1330T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593566 | |||||||
chr2:17593645 | G | A | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1409G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593645 | |||||||
chr2:17593765 | A | G | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.162+1529A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593765 | |||||||
chr2:17593894 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.162+1658C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593894 | |||||||
chr2:17593938 | T | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+1702T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593938 | |||||||
chr2:17593995 | G | C | 2 | a0001c0001t0012g0144 a0001c0001t0012g0188 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1759G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17593995 | |||||||
chr2:17594122 | C | T | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+1886C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594122 | |||||||
chr2:17594192 | T | C | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162+1956T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594192 | |||||||
chr2:17594440 | A | C | 1 | a0001c0001t0004g0201 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.162+2204A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594440 | |||||||
chr2:17594457 | C | G | 1 | a0001c0001t0026g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+2221C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594457 | |||||||
chr2:17594526 | T | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+2290T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594526 | |||||||
chr2:17594561 | G | A | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+2325G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594561 | |||||||
chr2:17594573 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2337G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594573 | |||||||
chr2:17594578 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.162+2342A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594578 | |||||||
chr2:17594663 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2427G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594663 | |||||||
chr2:17594701 | C | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 |
3 | HG00741.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.162+2465C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594701 | |||||||
chr2:17594736 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.162+2500A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594736 | |||||||
chr2:17594786 | G | A | 45 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.162+2550G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594786 | |||||||
chr2:17594811 | G | A | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.162+2575G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17594811 | |||||||
chr2:17595159 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2923C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595159 | |||||||
chr2:17595397 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162+3161C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595397 | |||||||
chr2:17595482 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.162+3246A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595482 | |||||||
chr2:17595539 | A | G | 1 | a0001c0001t0012g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162+3303A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595539 | |||||||
chr2:17595721 | TG | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+3486delG | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595721 | |||||||
chr2:17595730 | G | A | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+3494G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595730 | |||||||
chr2:17595851 | A | G | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+3615A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595851 | |||||||
chr2:17595947 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.162+3711C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17595947 | |||||||
chr2:17596101 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0159 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+3865A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596101 | |||||||
chr2:17596122 | T | C | 4 | a0001c0001t0004g0173 a0001c0001t0011g0113 a0001c0001t0011g0189 others(1): Show |
4 | HG00639.hp1 HG01074.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+3886T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596122 | |||||||
chr2:17596151 | A | G | 1 | a0001c0001t0021g0191 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.162+3915A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596151 | |||||||
chr2:17596169 | C | T | 1 | a0001c0001t0007g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+3933C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596169 | |||||||
chr2:17596223 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0005g0187 |
2 | HG01069.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.162+3987C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596223 | |||||||
chr2:17596224 | G | A | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+3988G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596224 | |||||||
chr2:17596457 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+4221C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596457 | |||||||
chr2:17596458 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+4222A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596458 | |||||||
chr2:17596459 | C | T | 1 | a0001c0001t0005g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.162+4223C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596459 | |||||||
chr2:17596679 | A | T | 1 | a0001c0001t0005g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162+4443A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596679 | |||||||
chr2:17596760 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+4524G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596760 | |||||||
chr2:17596774 | TGA | T | 11 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(8): Show |
15 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.162+4542_162+4543d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17596774 | ||||||
chr2:17596817 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.162+4581A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596817 | |||||||
chr2:17596862 | C | T | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+4626C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596862 | |||||||
chr2:17596959 | A | C | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+4723A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17596959 | |||||||
chr2:17597013 | C | T | 1 | a0001c0001t0015g0152 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.162+4777C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597013 | |||||||
chr2:17597021 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+4785G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597021 | |||||||
chr2:17597022 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+4786A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597022 | |||||||
chr2:17597062 | C | G | 37 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(34): Show |
38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+4826C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597062 | |||||||
chr2:17597062 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.162+4826C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597062 | |||||||
chr2:17597237 | C | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+5001C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597237 | |||||||
chr2:17597441 | C | T | 37 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(34): Show |
38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+5205C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597441 | |||||||
chr2:17597511 | C | G | 37 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(34): Show |
38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+5275C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597511 | |||||||
chr2:17597515 | T | A | 25 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(22): Show |
26 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.162+5279T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597515 | |||||||
chr2:17597676 | C | T | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+5440C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597676 | |||||||
chr2:17597677 | A | G | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.162+5441A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597677 | |||||||
chr2:17597755 | TC | T | 25 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(22): Show |
26 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.162+5520delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17597755 | |||||||
chr2:17598021 | A | T | 1 | a0001c0001t0017g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+5785A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598021 | |||||||
chr2:17598064 | G | A | 5 | a0001c0001t0016g0167 a0001c0001t0024g0164 a0001c0001t0024g0165 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+5828G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598064 | |||||||
chr2:17598374 | A | T | 37 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(34): Show |
38 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+6138A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598374 | |||||||
chr2:17598486 | C | G | 1 | a0001c0001t0044g0186 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.162+6250C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598486 | |||||||
chr2:17598534 | G | A | 1 | a0001c0001t0017g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+6298G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598534 | |||||||
chr2:17598552 | A | C | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+6316A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598552 | |||||||
chr2:17598575 | A | G | 1 | a0001c0001t0005g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162+6339A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598575 | |||||||
chr2:17598738 | A | C | 1 | a0001c0001t0017g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+6502A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598738 | |||||||
chr2:17598739 | G | T | 1 | a0001c0001t0002g0145 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+6503G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598739 | |||||||
chr2:17598814 | C | G | 43 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0005g0157 others(40): Show |
43 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.162+6578C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17598814 | |||||||
chr2:17599022 | C | T | 1 | a0001c0001t0035g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.162+6786C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599022 | |||||||
chr2:17599156 | G | C | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+6920G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599156 | |||||||
chr2:17599193 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.162+6957C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599193 | |||||||
chr2:17599216 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+6980G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599216 | |||||||
chr2:17599413 | A | G | 6 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 others(3): Show |
6 | HG01496.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+7177A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599413 | |||||||
chr2:17599417 | T | C | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+7181T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599417 | |||||||
chr2:17599424 | T | A | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+7188T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599424 | |||||||
chr2:17599446 | T | C | 11 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(8): Show |
15 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.162+7210T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599446 | |||||||
chr2:17599466 | T | A | 34 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(31): Show |
39 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.162+7230T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599466 | |||||||
chr2:17599594 | C | G | 83 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(80): Show |
86 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.162+7358C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17599594 | |||||||
chr2:17600064 | A | T | 1 | a0001c0001t0006g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162+7828A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600064 | |||||||
chr2:17600112 | A | G | 1 | a0001c0001t0019g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.162+7876A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600112 | |||||||
chr2:17600124 | T | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+7888T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600124 | |||||||
chr2:17600295 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162+8059G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600295 | |||||||
chr2:17600537 | T | G | 2 | a0001c0001t0003g0007 a0001c0001t0014g0105 |
3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.162+8301T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600537 | |||||||
chr2:17600619 | T | C | 1 | a0001c0001t0009g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+8383T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17600619 | |||||||
chr2:17601052 | A | T | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+8816A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601052 | |||||||
chr2:17601289 | A | T | 163 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.162+9053A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601289 | |||||||
chr2:17601596 | A | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+9360A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601596 | |||||||
chr2:17601627 | C | T | 4 | a0001c0001t0007g0198 a0001c0001t0007g0203 a0001c0001t0007g0204 others(1): Show |
4 | HG01891.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+9391C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601627 | |||||||
chr2:17601657 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+9421A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601657 | |||||||
chr2:17601923 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+9687G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17601923 | |||||||
chr2:17602186 | C | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+9950C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602186 | |||||||
chr2:17602211 | G | A | 2 | a0001c0001t0012g0144 a0001c0001t0012g0188 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+9975G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602211 | |||||||
chr2:17602574 | C | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+10338C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602574 | |||||||
chr2:17602614 | C | G | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+10378C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602614 | |||||||
chr2:17602697 | G | A | 4 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(1): Show |
6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+10461G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602697 | |||||||
chr2:17602763 | TAAAATAA others(1): Show |
T | 23 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+10537_162+1054 others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17602763 | ||||||
chr2:17602890 | T | C | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+10654T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602890 | |||||||
chr2:17602891 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+10655G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602891 | |||||||
chr2:17602927 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+10691A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602927 | |||||||
chr2:17602936 | C | T | 4 | a0001c0001t0004g0173 a0001c0001t0011g0113 a0001c0001t0011g0189 others(1): Show |
4 | HG00639.hp1 HG01074.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+10700C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602936 | |||||||
chr2:17602968 | A | G | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+10732A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17602968 | |||||||
chr2:17603052 | G | A | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+10816G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603052 | |||||||
chr2:17603336 | G | T | 34 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0005g0157 others(31): Show |
34 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.162+11100G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603336 | |||||||
chr2:17603514 | C | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+11278C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603514 | |||||||
chr2:17603719 | C | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+11483C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603719 | |||||||
chr2:17603856 | C | T | 21 | a0001c0001t0004g0201 a0001c0001t0006g0216 a0001c0001t0006g0217 others(18): Show |
21 | HG01099.hp1 HG01243.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.162+11620C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17603856 | |||||||
chr2:17604113 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+11877G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604113 | |||||||
chr2:17604190 | A | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.162+11954A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604190 | |||||||
chr2:17604249 | T | G | 9 | a0001c0001t0003g0103 a0001c0001t0006g0070 a0001c0001t0013g0068 others(6): Show |
9 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+12013T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604249 | |||||||
chr2:17604263 | G | C | 2 | a0001c0001t0008g0114 a0001c0001t0008g0115 |
2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.162+12027G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604263 | |||||||
chr2:17604320 | T | A | 1 | a0001c0001t0021g0191 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.162+12084T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604320 | |||||||
chr2:17604599 | C | T | 1 | a0001c0001t0026g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+12363C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604599 | |||||||
chr2:17604686 | G | A | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+12450G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604686 | |||||||
chr2:17604720 | G | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+12484G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604720 | |||||||
chr2:17604990 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.162+12754T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17604990 | |||||||
chr2:17605038 | C | T | 4 | a0001c0001t0004g0022 a0001c0001t0004g0024 a0001c0001t0006g0027 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+12802C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605038 | |||||||
chr2:17605195 | G | A | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+12959G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605195 | |||||||
chr2:17605261 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162+13025A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605261 | |||||||
chr2:17605291 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13055G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605291 | |||||||
chr2:17605292 | C | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+13056C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605292 | |||||||
chr2:17605337 | A | G | 1 | a0001c0001t0015g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.162+13101A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605337 | |||||||
chr2:17605364 | C | G | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+13128C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605364 | |||||||
chr2:17605392 | CT | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13158delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17605392 | ||||||
chr2:17605464 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.162+13228A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605464 | |||||||
chr2:17605466 | C | T | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+13230C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605466 | |||||||
chr2:17605491 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13255G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605491 | |||||||
chr2:17605517 | C | T | 1 | a0001c0001t0023g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.162+13281C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605517 | |||||||
chr2:17605569 | G | A | 1 | a0001c0001t0017g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+13333G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605569 | |||||||
chr2:17605829 | T | A | 4 | a0001c0001t0005g0157 a0001c0001t0010g0154 a0001c0001t0010g0177 others(1): Show |
4 | HG02145.hp1 HG02735.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+13593T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605829 | |||||||
chr2:17605933 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.162+13697G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605933 | |||||||
chr2:17605999 | C | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+13763C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17605999 | |||||||
chr2:17606186 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.162+13950C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606186 | |||||||
chr2:17606289 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+14053A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606289 | |||||||
chr2:17606308 | C | CA | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+14072_162+1407 others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606308 | |||||||
chr2:17606314 | C | G | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+14078C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606314 | |||||||
chr2:17606632 | A | G | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+14396A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606632 | |||||||
chr2:17606936 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.162+14700G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17606936 | |||||||
chr2:17607023 | A | G | 4 | a0001c0001t0006g0216 a0001c0001t0006g0217 a0001c0001t0006g0219 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+14787A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607023 | |||||||
chr2:17607161 | C | T | 34 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0005g0157 others(31): Show |
34 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.162+14925C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607161 | |||||||
chr2:17607202 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+14966A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607202 | |||||||
chr2:17607225 | G | A | 6 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 others(3): Show |
6 | HG01496.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+14989G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607225 | |||||||
chr2:17607476 | G | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+15240G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607476 | |||||||
chr2:17607487 | A | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+15251A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607487 | |||||||
chr2:17607523 | G | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+15287G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607523 | |||||||
chr2:17607836 | A | T | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+15600A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607836 | |||||||
chr2:17607846 | A | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+15610A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607846 | |||||||
chr2:17607853 | T | A | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+15617T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607853 | |||||||
chr2:17607887 | A | T | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+15651A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607887 | |||||||
chr2:17607986 | C | T | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+15750C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17607986 | |||||||
chr2:17608087 | C | T | 1 | a0001c0001t0010g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162+15851C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608087 | |||||||
chr2:17608321 | G | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162+16085G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608321 | |||||||
chr2:17608337 | G | A | 6 | a0001c0001t0006g0070 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG00323.hp2 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+16101G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608337 | |||||||
chr2:17608461 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0159 others(2): Show |
5 | HG00099.hp1 HG01123.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+16225G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608461 | |||||||
chr2:17608866 | T | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+16630T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17608866 | |||||||
chr2:17609024 | T | A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+16788T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609024 | |||||||
chr2:17609045 | G | A | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162+16809G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609045 | |||||||
chr2:17609175 | C | G | 6 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0143 others(3): Show |
6 | HG00642.hp2 HG01168.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+16939C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609175 | |||||||
chr2:17609246 | C | T | 72 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(69): Show |
78 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.162+17010C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609246 | |||||||
chr2:17609368 | C | T | 1 | a0001c0001t0007g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+17132C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609368 | |||||||
chr2:17609504 | G | C | 6 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+17268G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609504 | |||||||
chr2:17609515 | T | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17279T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609515 | |||||||
chr2:17609609 | T | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17373T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609609 | |||||||
chr2:17609642 | A | C | 2 | a0001c0001t0006g0027 a0001c0001t0006g0028 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.162+17406A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609642 | |||||||
chr2:17609781 | C | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17545C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609781 | |||||||
chr2:17609914 | C | T | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+17678C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609914 | |||||||
chr2:17609940 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0017g0065 |
2 | HG02015.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162+17704C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609940 | |||||||
chr2:17609964 | T | G | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+17728T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609964 | |||||||
chr2:17609973 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+17737A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17609973 | |||||||
chr2:17610208 | A | G | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+17972A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610208 | |||||||
chr2:17610215 | T | C | 4 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(1): Show |
6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+17979T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610215 | |||||||
chr2:17610771 | G | T | 7 | a0001c0001t0003g0099 a0001c0001t0004g0096 a0001c0001t0004g0097 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+18535G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610771 | |||||||
chr2:17610948 | C | G | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+18712C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17610948 | |||||||
chr2:17611092 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+18856G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611092 | |||||||
chr2:17611312 | C | T | 1 | a0001c0001t0008g0130 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162+19076C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611312 | |||||||
chr2:17611431 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+19195G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611431 | |||||||
chr2:17611563 | C | T | 34 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0005g0157 others(31): Show |
34 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.162+19327C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611563 | |||||||
chr2:17611642 | ACT | A | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+19411_162+1941 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17611642 | ||||||
chr2:17611826 | A | G | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+19590A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611826 | |||||||
chr2:17611828 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.162+19592T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611828 | |||||||
chr2:17611861 | C | T | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+19625C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17611861 | |||||||
chr2:17612062 | C | CTG | 18 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(15): Show |
18 | HG00642.hp2 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.162+19837_162+1983 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17612062 | ||||||
chr2:17612062 | CTG | C | 29 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(26): Show |
30 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.162+19837_162+1983 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17612062 | ||||||
chr2:17612091 | T | C | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+19855T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612091 | |||||||
chr2:17612113 | G | A | 4 | a0001c0001t0006g0216 a0001c0001t0006g0217 a0001c0001t0006g0219 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+19877G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612113 | |||||||
chr2:17612115 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+19879G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612115 | |||||||
chr2:17612298 | G | A | 6 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+20062G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612298 | |||||||
chr2:17612430 | T | C | 163 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.162+20194T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612430 | |||||||
chr2:17612627 | C | T | 1 | a0001c0001t0010g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+20391C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612627 | |||||||
chr2:17612967 | G | A | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162+20731G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17612967 | |||||||
chr2:17613064 | A | G | 1 | a0001c0001t0038g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.162+20828A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613064 | |||||||
chr2:17613087 | G | A | 9 | a0001c0001t0003g0103 a0001c0001t0006g0070 a0001c0001t0013g0068 others(6): Show |
9 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+20851G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613087 | |||||||
chr2:17613137 | C | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+20901C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613137 | |||||||
chr2:17613205 | T | G | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.162+20969T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613205 | |||||||
chr2:17613383 | A | G | 1 | a0001c0001t0004g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.162+21147A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613383 | |||||||
chr2:17613462 | G | A | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+21226G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613462 | |||||||
chr2:17613530 | C | T | 4 | a0001c0001t0004g0173 a0001c0001t0011g0113 a0001c0001t0011g0189 others(1): Show |
4 | HG00639.hp1 HG01074.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+21294C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613530 | |||||||
chr2:17613635 | A | G | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+21399A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613635 | |||||||
chr2:17613640 | T | A | 2 | a0001c0001t0011g0092 a0001c0001t0011g0098 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.162+21404T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613640 | |||||||
chr2:17613741 | T | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+21505T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613741 | |||||||
chr2:17613757 | C | T | 16 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(13): Show |
20 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.162+21521C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17613757 | |||||||
chr2:17614018 | C | T | 4 | a0001c0001t0005g0157 a0001c0001t0010g0154 a0001c0001t0010g0177 others(1): Show |
4 | HG02145.hp1 HG02735.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+21782C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614018 | |||||||
chr2:17614030 | T | C | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+21794T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614030 | |||||||
chr2:17614342 | C | T | 9 | a0001c0001t0003g0103 a0001c0001t0006g0070 a0001c0001t0013g0068 others(6): Show |
9 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+22106C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614342 | |||||||
chr2:17614715 | A | T | 2 | a0001c0001t0014g0214 a0001c0001t0017g0213 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.162+22479A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614715 | |||||||
chr2:17614740 | C | A | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+22504C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614740 | |||||||
chr2:17614851 | G | A | 1 | a0001c0001t0032g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162+22615G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614851 | |||||||
chr2:17614898 | C | T | 130 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(127): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.162+22662C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614898 | |||||||
chr2:17614906 | A | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+22670A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614906 | |||||||
chr2:17614934 | T | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+22698T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17614934 | |||||||
chr2:17615038 | T | C | 1 | a0001c0001t0010g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+22802T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615038 | |||||||
chr2:17615120 | A | T | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.162+22884A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615120 | |||||||
chr2:17615248 | T | A | 1 | a0001c0001t0016g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.162+23012T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615248 | |||||||
chr2:17615250 | G | T | 1 | a0001c0001t0016g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.162+23014G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615250 | |||||||
chr2:17615557 | T | C | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+23321T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17615557 | |||||||
chr2:17616016 | T | C | 1 | a0001c0001t0009g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162+23780T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616016 | |||||||
chr2:17616193 | T | G | 1 | a0001c0001t0017g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+23957T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616193 | |||||||
chr2:17616210 | C | T | 1 | a0001c0001t0011g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.162+23974C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616210 | |||||||
chr2:17616241 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+24005G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616241 | |||||||
chr2:17616330 | G | A | 1 | a0001c0001t0012g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162+24094G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616330 | |||||||
chr2:17616391 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+24155C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616391 | |||||||
chr2:17616790 | C | T | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+24554C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616790 | |||||||
chr2:17616978 | G | GT | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+24742_162+2474 others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17616978 | |||||||
chr2:17617054 | C | G | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+24818C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617054 | |||||||
chr2:17617179 | G | A | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+24943G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617179 | |||||||
chr2:17617235 | C | T | 1 | a0001c0001t0031g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.162+24999C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617235 | |||||||
chr2:17617257 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.162+25021G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617257 | |||||||
chr2:17617262 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.162+25026A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617262 | |||||||
chr2:17617495 | TA | T | 29 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0212 others(26): Show |
29 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.162+25271delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617495 | ||||||
chr2:17617510 | G | A | 21 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(18): Show |
22 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.162+25274G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617510 | |||||||
chr2:17617627 | G | A | 1 | a0001c0001t0008g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162+25391G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617627 | |||||||
chr2:17617705 | G | A | 11 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(8): Show |
11 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+25469G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617705 | |||||||
chr2:17617737 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+25501G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617737 | |||||||
chr2:17617885 | A | ACACATGC others(15): Show |
24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+25650_162+2565 others(26): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617885 | ||||||
chr2:17617889 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+25653G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17617889 | |||||||
chr2:17617889 | G | GCA | 19 | a0001c0001t0004g0112 a0001c0001t0005g0187 a0001c0001t0006g0002 others(16): Show |
21 | HG01069.hp2 HG01934.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.162+25673_162+2567 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617889 | ||||||
chr2:17617889 | G | GCACA | 3 | a0001c0001t0020g0008 a0001c0001t0020g0117 a0001c0001t0022g0009 |
5 | HG02280.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+25671_162+2567 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17617889 | ||||||
chr2:17618021 | C | T | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.162+25785C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618021 | |||||||
chr2:17618034 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.162+25798T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618034 | |||||||
chr2:17618087 | C | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+25851C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618087 | |||||||
chr2:17618232 | T | G | 11 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(8): Show |
15 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.162+25996T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618232 | |||||||
chr2:17618294 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.162+26058A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618294 | |||||||
chr2:17618308 | T | C | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+26072T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618308 | |||||||
chr2:17618929 | T | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+26693T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17618929 | |||||||
chr2:17619011 | G | T | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.162+26775G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619011 | |||||||
chr2:17619115 | C | T | 8 | a0001c0001t0003g0103 a0001c0001t0006g0070 a0001c0001t0013g0068 others(5): Show |
8 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+26879C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619115 | |||||||
chr2:17619290 | C | G | 26 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0006g0216 others(23): Show |
26 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+27054C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619290 | |||||||
chr2:17619322 | C | T | 24 | a0001c0001t0004g0112 a0001c0001t0004g0173 a0001c0001t0006g0002 others(21): Show |
28 | HG00639.hp2 HG02055.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.162+27086C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619322 | |||||||
chr2:17619834 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
5 | HG00408.hp2 NA18612.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+27598G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619834 | |||||||
chr2:17619862 | TA | T | 6 | a0001c0001t0001g0049 a0001c0001t0002g0149 a0001c0001t0002g0150 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+27639delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17619862 | ||||||
chr2:17619862 | TAA | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+27638_162+2763 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17619862 | ||||||
chr2:17619881 | TC | T | 37 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0005g0157 others(34): Show |
37 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+27653delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17619881 | ||||||
chr2:17619888 | C | G | 2 | a0001c0001t0019g0195 a0001c0001t0043g0033 |
2 | HG03579.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.162+27652C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619888 | |||||||
chr2:17619888 | C | T | 47 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(44): Show |
48 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.162+27652C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17619888 | |||||||
chr2:17620130 | T | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+27894T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620130 | |||||||
chr2:17620221 | A | G | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.162+27985A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620221 | |||||||
chr2:17620566 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.162+28330G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620566 | |||||||
chr2:17620768 | CA | C | 5 | a0001c0001t0008g0129 a0001c0001t0008g0133 a0001c0001t0010g0116 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+28541delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17620768 | ||||||
chr2:17620917 | G | A | 45 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(42): Show |
47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-28493G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17620917 | |||||||
chr2:17621004 | C | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-28406C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621004 | |||||||
chr2:17621184 | C | T | 1 | a0001c0001t0007g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.163-28226C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621184 | |||||||
chr2:17621189 | A | G | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-28221A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621189 | |||||||
chr2:17621306 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-28104C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621306 | |||||||
chr2:17621312 | C | CCTTTTCT others(5): Show |
22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-28085_163-2807 others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17621312 | ||||||
chr2:17621549 | C | G | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-27861C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621549 | |||||||
chr2:17621651 | G | T | 1 | a0001c0001t0007g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163-27759G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621651 | |||||||
chr2:17621728 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-27682A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621728 | |||||||
chr2:17621834 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-27576C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17621834 | |||||||
chr2:17622208 | A | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-27202A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622208 | |||||||
chr2:17622212 | C | CA | 31 | a0001c0001t0001g0056 a0001c0001t0001g0212 a0001c0001t0003g0111 others(28): Show |
31 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.163-27182dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622212 | ||||||
chr2:17622212 | C | CAA | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-27183_163-2718 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622212 | ||||||
chr2:17622212 | CAA | C | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-27183_163-2718 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622212 | ||||||
chr2:17622334 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0030 others(1): Show |
5 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-27076C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622334 | |||||||
chr2:17622424 | G | A | 6 | a0001c0001t0003g0084 a0001c0001t0003g0085 a0001c0001t0003g0086 others(3): Show |
6 | HG00735.hp1 HG01433.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-26986G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622424 | |||||||
chr2:17622430 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-26980G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622430 | |||||||
chr2:17622440 | G | T | 22 | a0001c0001t0004g0201 a0001c0001t0006g0216 a0001c0001t0006g0217 others(19): Show |
22 | HG00639.hp1 HG01074.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.163-26970G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622440 | |||||||
chr2:17622441 | T | C | 1 | a0001c0001t0043g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.163-26969T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622441 | |||||||
chr2:17622453 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.163-26957G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622453 | |||||||
chr2:17622481 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-26929G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622481 | |||||||
chr2:17622497 | C | CA | 25 | a0001c0001t0003g0007 a0001c0001t0003g0084 a0001c0001t0003g0099 others(22): Show |
26 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-26901dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622497 | ||||||
chr2:17622504 | AAAAAAGA others(7): Show |
A | 3 | a0001c0001t0005g0157 a0001c0001t0017g0013 a0001c0001t0031g0156 |
3 | HG02735.hp2 HG02922.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.163-26901_163-2688 others(18): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622504 | ||||||
chr2:17622506 | AAAAGAAA others(5): Show |
A | 19 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 others(16): Show |
20 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.163-26900_163-2688 others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622506 | ||||||
chr2:17622507 | AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0004g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.163-26900_163-2689 others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622507 | ||||||
chr2:17622519 | AAAAGAAA others(54): Show |
A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-26875_163-2681 others(65): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622519 | ||||||
chr2:17622528 | AAAGAAAA others(21): Show |
A | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-26879_163-2685 others(32): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622528 | ||||||
chr2:17622528 | AAAGAAAA others(29): Show |
A | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-26879_163-2684 others(40): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622528 | ||||||
chr2:17622531 | GAAAAGAA others(20): Show |
G | 1 | a0001c0001t0010g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-26877_163-2685 others(31): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622531 | ||||||
chr2:17622532 | A | AAAAG | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(4): Show |
7 | HG00099.hp2 HG02015.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-26810_163-2680 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | A | AAAGAAAG others(4): Show |
2 | a0001c0001t0001g0051 a0001c0001t0028g0035 |
2 | HG01981.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.163-26876_163-2687 others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAG | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0036 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.163-26810_163-2680 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(1): Show |
A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0046 others(39): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.163-26814_163-2680 others(12): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(5): Show |
A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0037 others(26): Show |
29 | HG00280.hp1 HG00438.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.163-26818_163-2680 others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(9): Show |
A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0047 others(12): Show |
18 | HG00735.hp2 HG01074.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-26822_163-2680 others(20): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(13): Show |
A | 10 | a0001c0001t0002g0121 a0001c0001t0006g0219 a0001c0001t0007g0198 others(7): Show |
10 | HG00639.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-26826_163-2680 others(24): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(17): Show |
A | 7 | a0001c0001t0007g0203 a0001c0001t0007g0206 a0001c0001t0010g0116 others(4): Show |
7 | HG01099.hp1 HG01891.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-26830_163-2680 others(28): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(21): Show |
A | 6 | a0001c0001t0006g0070 a0001c0001t0007g0205 a0001c0001t0011g0109 others(3): Show |
6 | HG00323.hp2 HG00738.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-26834_163-2680 others(32): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622532 | AAAAGAAA others(25): Show |
A | 4 | a0001c0001t0003g0084 a0001c0001t0011g0092 a0001c0001t0011g0098 others(1): Show |
4 | HG01516.hp2 HG02886.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-26838_163-2680 others(36): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622532 | ||||||
chr2:17622542 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0019g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.163-26866_163-2685 others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622542 | ||||||
chr2:17622545 | AAAG | A | 4 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0005g0157 others(1): Show |
4 | HG01192.hp1 HG02723.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-26862_163-2686 others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622545 | ||||||
chr2:17622545 | AAAGAAAG | A | 7 | a0001c0001t0003g0074 a0001c0001t0003g0085 a0001c0001t0003g0086 others(4): Show |
7 | HG01175.hp1 HG01981.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-26862_163-2685 others(11): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622545 | ||||||
chr2:17622545 | AAAGAAAG others(4): Show |
A | 11 | a0001c0001t0003g0087 a0001c0001t0003g0089 a0001c0001t0003g0103 others(8): Show |
12 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-26862_163-2685 others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622545 | ||||||
chr2:17622576 | GAAAGAAA others(18): Show |
G | 1 | a0001c0001t0014g0100 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.163-26820_163-2679 others(29): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622576 | ||||||
chr2:17622600 | GA | G | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0158 others(20): Show |
24 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-26806delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17622600 | ||||||
chr2:17622604 | A | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-26806A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622604 | |||||||
chr2:17622613 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-26797G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622613 | |||||||
chr2:17622826 | G | C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-26584G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622826 | |||||||
chr2:17622842 | C | T | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-26568C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622842 | |||||||
chr2:17622877 | G | A | 9 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(6): Show |
9 | HG01934.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-26533G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17622877 | |||||||
chr2:17623169 | T | TA | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-26233dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623169 | ||||||
chr2:17623170 | A | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.163-26240A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623170 | |||||||
chr2:17623273 | A | G | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-26137A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623273 | |||||||
chr2:17623318 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-26092G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623318 | |||||||
chr2:17623397 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-26013C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623397 | |||||||
chr2:17623399 | G | A | 1 | a0001c0001t0023g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163-26011G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623399 | |||||||
chr2:17623432 | G | C | 1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-25978G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623432 | |||||||
chr2:17623458 | A | G | 2 | a0001c0001t0012g0144 a0001c0001t0012g0188 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.163-25952A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623458 | |||||||
chr2:17623486 | G | A | 9 | a0001c0001t0003g0103 a0001c0001t0006g0070 a0001c0001t0013g0068 others(6): Show |
9 | HG00323.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-25924G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623486 | |||||||
chr2:17623493 | C | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-25917C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623493 | |||||||
chr2:17623562 | C | T | 1 | a0001c0001t0007g0006 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.163-25848C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623562 | |||||||
chr2:17623602 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163-25808G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623602 | |||||||
chr2:17623604 | A | C | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-25806A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623604 | |||||||
chr2:17623638 | G | C | 153 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(150): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.163-25772G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623638 | |||||||
chr2:17623648 | C | T | 1 | a0001c0001t0016g0041 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.163-25762C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623648 | |||||||
chr2:17623669 | C | CA | 25 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0046 others(22): Show |
25 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-25718dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623669 | ||||||
chr2:17623669 | CA | C | 75 | a0001c0001t0001g0034 a0001c0001t0002g0038 a0001c0001t0002g0039 others(72): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.163-25718delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623669 | ||||||
chr2:17623669 | CAA | C | 36 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(33): Show |
37 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.163-25719_163-2571 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17623669 | ||||||
chr2:17623959 | T | G | 2 | a0001c0001t0003g0007 a0001c0001t0014g0105 |
3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-25451T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17623959 | |||||||
chr2:17624387 | A | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-25023A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624387 | |||||||
chr2:17624401 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.163-25009A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624401 | |||||||
chr2:17624512 | T | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24898T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624512 | |||||||
chr2:17624519 | T | G | 1 | a0001c0001t0005g0021 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163-24891T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624519 | |||||||
chr2:17624592 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.163-24818G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624592 | |||||||
chr2:17624611 | G | A | 8 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(5): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-24799G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624611 | |||||||
chr2:17624677 | A | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24733A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624677 | |||||||
chr2:17624732 | A | G | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-24678A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624732 | |||||||
chr2:17624896 | A | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24514A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17624896 | |||||||
chr2:17625054 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-24356G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625054 | |||||||
chr2:17625087 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163-24323T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625087 | |||||||
chr2:17625145 | G | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-24265G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625145 | |||||||
chr2:17625162 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163-24248G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625162 | |||||||
chr2:17625312 | A | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24098A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625312 | |||||||
chr2:17625387 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-24023C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625387 | |||||||
chr2:17625493 | T | C | 2 | a0001c0001t0029g0208 a0001c0001t0042g0210 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.163-23917T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625493 | |||||||
chr2:17625840 | A | AT | 33 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0052 others(30): Show |
36 | HG00639.hp2 HG00735.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-23547dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | ||||||
chr2:17625840 | A | ATT | 6 | a0001c0001t0004g0112 a0001c0001t0005g0187 a0001c0001t0010g0126 others(3): Show |
7 | HG01069.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-23548_163-2354 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | ||||||
chr2:17625840 | AT | A | 71 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-23547delT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | ||||||
chr2:17625840 | ATT | A | 10 | a0001c0001t0002g0139 a0001c0001t0005g0181 a0001c0001t0006g0216 others(7): Show |
11 | HG00408.hp1 HG02698.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-23548_163-2354 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17625840 | ||||||
chr2:17625888 | C | T | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-23522C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17625888 | |||||||
chr2:17626021 | G | T | 1 | a0001c0001t0005g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163-23389G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626021 | |||||||
chr2:17626170 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-23240G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626170 | |||||||
chr2:17626202 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-23208C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626202 | |||||||
chr2:17626312 | T | C | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-23098T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626312 | |||||||
chr2:17626359 | A | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-23051A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626359 | |||||||
chr2:17626499 | T | C | 2 | a0001c0001t0024g0164 a0001c0001t0024g0165 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.163-22911T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626499 | |||||||
chr2:17626603 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.163-22807A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626603 | |||||||
chr2:17626764 | T | C | 2 | a0001c0001t0005g0187 a0001c0001t0023g0083 |
2 | HG01069.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.163-22646T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626764 | |||||||
chr2:17626849 | AATG | A | 11 | a0001c0001t0004g0201 a0001c0001t0007g0196 a0001c0001t0007g0198 others(8): Show |
11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-22556_163-2255 others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17626849 | ||||||
chr2:17626866 | G | C | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-22544G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626866 | |||||||
chr2:17626917 | G | C | 26 | a0001c0001t0001g0212 a0001c0001t0004g0201 a0001c0001t0006g0216 others(23): Show |
26 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-22493G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17626917 | |||||||
chr2:17627174 | T | A | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.163-22236T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627174 | |||||||
chr2:17627284 | C | T | 45 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(42): Show |
47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-22126C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627284 | |||||||
chr2:17627330 | A | G | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-22080A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627330 | |||||||
chr2:17627904 | C | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-21506C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17627904 | |||||||
chr2:17628218 | C | T | 1 | a0001c0001t0011g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.163-21192C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628218 | |||||||
chr2:17628226 | C | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0176 |
3 | NA18967.hp2 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.163-21184C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628226 | |||||||
chr2:17628274 | T | G | 2 | a0001c0001t0014g0081 a0001c0001t0014g0100 |
2 | NA18955.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.163-21136T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628274 | |||||||
chr2:17628361 | G | A | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-21049G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628361 | |||||||
chr2:17628396 | A | G | 1 | a0001c0001t0007g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163-21014A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628396 | |||||||
chr2:17628480 | A | G | 4 | a0001c0001t0029g0208 a0001c0001t0029g0211 a0001c0001t0041g0209 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-20930A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628480 | |||||||
chr2:17628509 | C | CA | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-20900dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17628509 | ||||||
chr2:17628629 | C | T | 1 | a0001c0001t0031g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.163-20781C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17628629 | |||||||
chr2:17629035 | G | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-20375G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629035 | |||||||
chr2:17629261 | A | C | 57 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(54): Show |
59 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.163-20149A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629261 | |||||||
chr2:17629378 | T | C | 2 | a0001c0001t0021g0090 a0001c0001t0021g0091 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.163-20032T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629378 | |||||||
chr2:17629555 | T | C | 45 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(42): Show |
47 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-19855T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629555 | |||||||
chr2:17629575 | C | T | 2 | a0001c0001t0023g0132 a0001c0001t0037g0127 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.163-19835C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629575 | |||||||
chr2:17629727 | C | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-19683C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629727 | |||||||
chr2:17629835 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-19575C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629835 | |||||||
chr2:17629859 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-19551G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629859 | |||||||
chr2:17629971 | T | C | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.163-19439T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17629971 | |||||||
chr2:17630015 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0032g0207 |
2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.163-19395G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630015 | |||||||
chr2:17630087 | C | A | 116 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(113): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.163-19323C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630087 | |||||||
chr2:17630111 | A | C | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.163-19299A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630111 | |||||||
chr2:17630209 | T | C | 6 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-19201T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630209 | |||||||
chr2:17630463 | A | G | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-18947A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630463 | |||||||
chr2:17630679 | G | A | 11 | a0001c0001t0004g0201 a0001c0001t0007g0196 a0001c0001t0007g0198 others(8): Show |
11 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-18731G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630679 | |||||||
chr2:17630749 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-18661C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630749 | |||||||
chr2:17630961 | T | C | 2 | a0001c0001t0003g0007 a0001c0001t0014g0105 |
3 | HG02717.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-18449T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17630961 | |||||||
chr2:17631026 | C | T | 1 | a0001c0001t0017g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.163-18384C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631026 | |||||||
chr2:17631074 | G | A | 1 | a0001c0001t0017g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-18336G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631074 | |||||||
chr2:17631275 | C | T | 3 | a0001c0001t0011g0113 a0001c0001t0011g0189 a0001c0001t0011g0190 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.163-18135C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631275 | |||||||
chr2:17631361 | A | G | 4 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(1): Show |
6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-18049A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631361 | |||||||
chr2:17631614 | T | A | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-17796T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631614 | |||||||
chr2:17631623 | C | T | 2 | a0001c0001t0009g0169 a0001c0001t0009g0170 |
2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.163-17787C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631623 | |||||||
chr2:17631675 | T | C | 7 | a0001c0001t0006g0216 a0001c0001t0006g0217 a0001c0001t0006g0219 others(4): Show |
7 | HG00639.hp1 HG01074.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-17735T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631675 | |||||||
chr2:17631764 | G | A | 46 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(43): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-17646G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631764 | |||||||
chr2:17631805 | C | T | 1 | a0001c0001t0007g0202 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.163-17605C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631805 | |||||||
chr2:17631806 | G | A | 24 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0121 others(21): Show |
24 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-17604G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631806 | |||||||
chr2:17631823 | A | C | 164 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(161): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.163-17587A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631823 | |||||||
chr2:17631973 | G | A | 1 | a0001c0001t0005g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163-17437G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17631973 | |||||||
chr2:17632003 | C | T | 4 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0023g0011 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-17407C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632003 | |||||||
chr2:17632011 | C | T | 18 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0135 others(15): Show |
18 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-17399C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632011 | |||||||
chr2:17632012 | A | G | 145 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(142): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.163-17398A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632012 | |||||||
chr2:17632252 | T | A | 5 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0017g0065 others(2): Show |
5 | HG02572.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-17158T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632252 | |||||||
chr2:17632280 | T | G | 1 | a0001c0001t0005g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163-17130T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632280 | |||||||
chr2:17632403 | T | C | 170 | a0001c0001t0001g0017 a0001c0001t0001g0124 a0001c0001t0001g0168 others(167): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.163-17007T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632403 | |||||||
chr2:17632466 | A | G | 17 | a0001c0001t0006g0219 a0001c0001t0008g0003 a0001c0001t0008g0012 others(14): Show |
17 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-16944A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632466 | |||||||
chr2:17632483 | T | C | 6 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(3): Show |
6 | HG01109.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-16927T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632483 | |||||||
chr2:17632607 | A | G | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-16803A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632607 | |||||||
chr2:17632763 | T | C | 170 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(167): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.163-16647T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17632763 | |||||||
chr2:17633109 | C | T | 13 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(10): Show |
13 | HG01934.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-16301C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633109 | |||||||
chr2:17633321 | C | T | 3 | a0001c0001t0010g0154 a0001c0001t0010g0177 a0001c0001t0031g0156 |
3 | HG02145.hp1 HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.163-16089C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633321 | |||||||
chr2:17633347 | A | G | 1 | a0001c0001t0005g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.163-16063A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633347 | |||||||
chr2:17633348 | CA | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.163-16038delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17633348 | ||||||
chr2:17633348 | CAA | C | 41 | a0001c0001t0001g0159 a0001c0001t0002g0137 a0001c0001t0002g0143 others(38): Show |
41 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.163-16039_163-1603 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17633348 | ||||||
chr2:17633428 | A | C | 6 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(3): Show |
6 | HG00639.hp2 NA18945.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-15982A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633428 | |||||||
chr2:17633882 | C | G | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.163-15528C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633882 | |||||||
chr2:17633921 | A | G | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-15489A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17633921 | |||||||
chr2:17634462 | C | T | 1 | a0001c0001t0005g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.163-14948C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634462 | |||||||
chr2:17634506 | G | C | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-14904G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634506 | |||||||
chr2:17634567 | G | A | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.163-14843G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634567 | |||||||
chr2:17634588 | T | C | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-14822T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634588 | |||||||
chr2:17634790 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.163-14620C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634790 | |||||||
chr2:17634866 | G | A | 1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-14544G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634866 | |||||||
chr2:17634874 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.163-14536G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634874 | |||||||
chr2:17634898 | G | A | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
23 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-14512G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634898 | |||||||
chr2:17634927 | C | T | 1 | a0001c0001t0004g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163-14483C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634927 | |||||||
chr2:17634991 | T | C | 2 | a0001c0001t0033g0199 a0001c0001t0034g0107 |
2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-14419T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17634991 | |||||||
chr2:17635059 | A | G | 90 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(87): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.163-14351A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635059 | |||||||
chr2:17635209 | C | A | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-14201C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635209 | |||||||
chr2:17635220 | A | G | 19 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(16): Show |
19 | HG01109.hp2 HG01934.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-14190A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635220 | |||||||
chr2:17635515 | C | A | 1 | a0001c0001t0009g0178 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163-13895C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635515 | |||||||
chr2:17635567 | A | G | 1 | a0001c0001t0016g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-13843A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635567 | |||||||
chr2:17635645 | T | C | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-13765T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17635645 | |||||||
chr2:17636045 | A | C | 19 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(16): Show |
19 | HG01109.hp2 HG01934.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-13365A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636045 | |||||||
chr2:17636065 | C | G | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-13345C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636065 | |||||||
chr2:17636106 | T | C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-13304T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636106 | |||||||
chr2:17636108 | T | A | 8 | a0001c0001t0004g0112 a0001c0001t0005g0187 a0001c0001t0006g0002 others(5): Show |
10 | HG01069.hp2 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-13302T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636108 | |||||||
chr2:17636263 | A | G | 1 | a0001c0001t0011g0102 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.163-13147A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636263 | |||||||
chr2:17636571 | G | A | 42 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(39): Show |
43 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-12839G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636571 | |||||||
chr2:17636722 | ATT | A | 161 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0059 others(158): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.163-12677_163-1267 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17636722 | ||||||
chr2:17636722 | ATTT | A | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(8): Show |
11 | HG02015.hp2 HG02056.hp1 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-12678_163-1267 others(7): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17636722 | ||||||
chr2:17636817 | G | A | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.163-12593G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636817 | |||||||
chr2:17636832 | G | T | 5 | a0001c0001t0016g0167 a0001c0001t0024g0164 a0001c0001t0024g0165 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-12578G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636832 | |||||||
chr2:17636895 | T | C | 10 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(7): Show |
10 | HG02015.hp2 HG02056.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-12515T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17636895 | |||||||
chr2:17637205 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-12205G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637205 | |||||||
chr2:17637271 | C | T | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-12139C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637271 | |||||||
chr2:17637272 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-12138G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637272 | |||||||
chr2:17637365 | CAG | C | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-12042_163-1204 others(6): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17637365 | ||||||
chr2:17637586 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-11824T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637586 | |||||||
chr2:17637616 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.163-11794G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637616 | |||||||
chr2:17637752 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-11658C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17637752 | |||||||
chr2:17638057 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-11353A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638057 | |||||||
chr2:17638142 | A | G | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-11268A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638142 | |||||||
chr2:17638182 | CACTA | C | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163-11222_163-1121 others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17638182 | ||||||
chr2:17638562 | G | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-10848G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638562 | |||||||
chr2:17638703 | C | A | 1 | a0001c0001t0010g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-10707C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638703 | |||||||
chr2:17638909 | A | G | 2 | a0001c0001t0011g0102 a0001c0001t0011g0109 |
2 | HG01070.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.163-10501A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17638909 | |||||||
chr2:17639050 | T | C | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-10360T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639050 | |||||||
chr2:17639178 | T | C | 1 | a0001c0001t0009g0178 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163-10232T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639178 | |||||||
chr2:17639471 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.163-9939A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639471 | |||||||
chr2:17639789 | A | T | 45 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(42): Show |
46 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.163-9621A>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639789 | |||||||
chr2:17639890 | C | A | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.163-9520C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639890 | |||||||
chr2:17639916 | CA | C | 2 | a0001c0001t0017g0013 a0001c0001t0017g0213 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.163-9493delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17639916 | |||||||
chr2:17640067 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.163-9343C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640067 | |||||||
chr2:17640110 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.163-9300C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640110 | |||||||
chr2:17640207 | C | T | 2 | a0001c0001t0014g0081 a0001c0001t0014g0100 |
2 | NA18955.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.163-9203C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640207 | |||||||
chr2:17640252 | C | CA | 68 | a0001c0001t0001g0049 a0001c0001t0003g0007 a0001c0001t0003g0074 others(65): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.163-9141dupA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17640252 | ||||||
chr2:17640270 | G | A | 12 | a0001c0001t0004g0173 a0001c0001t0016g0041 a0001c0001t0016g0153 others(9): Show |
12 | HG00639.hp2 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-9140G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640270 | |||||||
chr2:17640554 | C | T | 1 | a0001c0001t0015g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.163-8856C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640554 | |||||||
chr2:17640699 | T | C | 18 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-8711T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17640699 | |||||||
chr2:17641322 | G | C | 1 | a0001c0001t0043g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.163-8088G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17641322 | |||||||
chr2:17641385 | A | G | 1 | a0001c0001t0013g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163-8025A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17641385 | |||||||
chr2:17641408 | A | G | 38 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0059 others(35): Show |
39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-8002A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17641408 | |||||||
chr2:17642042 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.163-7368T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642042 | |||||||
chr2:17642080 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-7330A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642080 | |||||||
chr2:17642225 | G | A | 32 | a0001c0001t0007g0006 a0001c0001t0007g0196 a0001c0001t0007g0198 others(29): Show |
33 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-7185G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642225 | |||||||
chr2:17642309 | C | CT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
10 | HG02015.hp2 HG04204.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-7084dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTT | 7 | a0001c0001t0003g0074 a0001c0001t0020g0008 a0001c0001t0020g0117 others(4): Show |
9 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-7086_163-7084d others(5): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTT | 14 | a0001c0001t0003g0007 a0001c0001t0003g0075 a0001c0001t0003g0076 others(11): Show |
15 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-7089_163-7084d others(8): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(4): Show |
9 | a0001c0001t0016g0041 a0001c0001t0016g0161 a0001c0001t0016g0163 others(6): Show |
9 | HG00639.hp2 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-7094_163-7084d others(13): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0022 a0001c0001t0004g0024 a0001c0001t0016g0153 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-7095_163-7084d others(14): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0004g0020 a0001c0001t0004g0032 a0001c0001t0006g0027 |
3 | HG01258.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.163-7096_163-7084d others(15): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0013g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.163-7097_163-7084d others(16): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0040g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.163-7100_163-7084d others(19): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(20): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(12): Show |
10 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0122 others(7): Show |
10 | HG02129.hp2 HG02155.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(21): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(13): Show |
21 | a0001c0001t0002g0059 a0001c0001t0002g0121 a0001c0001t0002g0136 others(18): Show |
22 | HG00408.hp1 HG00642.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(22): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(14): Show |
11 | a0001c0001t0002g0135 a0001c0001t0002g0140 a0001c0001t0002g0141 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(23): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-7084_163-7083i others(24): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0005g0095 a0001c0001t0006g0028 a0001c0001t0013g0094 |
3 | HG01257.hp1 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.163-7084_163-7083i others(25): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0013g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(26): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(18): Show |
5 | a0001c0001t0004g0097 a0001c0001t0006g0070 a0001c0001t0013g0068 others(2): Show |
5 | HG00738.hp1 HG01192.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(27): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0004g0096 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(28): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-7084_163-7083i others(29): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(21): Show |
6 | a0001c0001t0004g0104 a0001c0001t0004g0106 a0001c0001t0004g0201 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-7084_163-7083i others(30): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(22): Show |
3 | a0001c0001t0003g0099 a0001c0001t0004g0110 a0001c0001t0006g0219 |
3 | HG03209.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.163-7084_163-7083i others(31): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0006g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163-7084_163-7083i others(35): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642309 | CTT | C | 35 | a0001c0001t0007g0006 a0001c0001t0007g0196 a0001c0001t0007g0198 others(32): Show |
36 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-7085_163-7084d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17642309 | ||||||
chr2:17642324 | T | C | 4 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(1): Show |
6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-7086T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642324 | |||||||
chr2:17642509 | C | T | 1 | a0001c0001t0016g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.163-6901C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642509 | |||||||
chr2:17642523 | T | C | 8 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(5): Show |
8 | HG01109.hp2 HG02258.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-6887T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642523 | |||||||
chr2:17642530 | G | A | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-6880G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642530 | |||||||
chr2:17642554 | C | T | 2 | a0001c0001t0018g0057 a0001c0001t0019g0045 |
2 | HG02155.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.163-6856C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642554 | |||||||
chr2:17642600 | G | A | 98 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(95): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.163-6810G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642600 | |||||||
chr2:17642702 | G | A | 1 | a0001c0001t0021g0192 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.163-6708G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642702 | |||||||
chr2:17642714 | C | G | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(8): Show |
11 | HG02015.hp2 HG02056.hp1 HG03579.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-6696C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642714 | |||||||
chr2:17642848 | T | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(5): Show |
8 | HG02015.hp2 HG02056.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-6562T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17642848 | |||||||
chr2:17643069 | ATG | A | 3 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.163-6337_163-6336d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 17643069 | ||||||
chr2:17643102 | C | A | 1 | a0001c0001t0005g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163-6308C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643102 | |||||||
chr2:17643113 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.163-6297G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643113 | |||||||
chr2:17643219 | T | A | 2 | a0001c0001t0009g0185 a0001c0001t0044g0186 |
2 | NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.163-6191T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643219 | |||||||
chr2:17643353 | C | T | 1 | a0001c0001t0018g0179 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.163-6057C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643353 | |||||||
chr2:17643416 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-5994A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643416 | |||||||
chr2:17643628 | C | T | 4 | a0001c0001t0006g0216 a0001c0001t0006g0217 a0001c0001t0006g0219 others(1): Show |
4 | HG03041.hp2 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-5782C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643628 | |||||||
chr2:17643643 | C | T | 1 | a0001c0001t0039g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.163-5767C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643643 | |||||||
chr2:17643836 | A | G | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-5574A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643836 | |||||||
chr2:17643913 | C | T | 48 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(45): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.163-5497C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17643913 | |||||||
chr2:17644036 | CTT | C | 2 | a0001c0001t0017g0013 a0001c0001t0017g0213 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.163-5373_163-5372d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644036 | |||||||
chr2:17644079 | G | A | 31 | a0001c0001t0007g0006 a0001c0001t0007g0196 a0001c0001t0007g0198 others(28): Show |
32 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.163-5331G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644079 | |||||||
chr2:17644725 | T | G | 13 | a0001c0001t0007g0006 a0001c0001t0010g0077 a0001c0001t0010g0078 others(10): Show |
14 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.163-4685T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644725 | |||||||
chr2:17644751 | C | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-4659C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644751 | |||||||
chr2:17644764 | A | G | 3 | a0001c0001t0003g0085 a0001c0001t0003g0086 a0001c0001t0003g0103 |
3 | HG01109.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.163-4646A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17644764 | |||||||
chr2:17645111 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.163-4299T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645111 | |||||||
chr2:17645184 | T | C | 2 | a0001c0001t0009g0185 a0001c0001t0044g0186 |
2 | NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.163-4226T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645184 | |||||||
chr2:17645310 | C | T | 8 | a0001c0001t0008g0003 a0001c0001t0008g0012 a0001c0001t0008g0114 others(5): Show |
8 | HG01109.hp2 HG02258.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-4100C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645310 | |||||||
chr2:17645577 | C | T | 7 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-3833C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645577 | |||||||
chr2:17645850 | CA | C | 56 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.163-3559delA | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17645850 | |||||||
chr2:17646158 | AC | A | 4 | a0001c0001t0004g0112 a0001c0001t0006g0002 a0001c0001t0006g0119 others(1): Show |
6 | HG02055.hp2 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3251delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646158 | |||||||
chr2:17646568 | A | G | 10 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(7): Show |
10 | HG02015.hp2 HG02056.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2842A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646568 | |||||||
chr2:17646753 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.163-2657T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646753 | |||||||
chr2:17646758 | C | T | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-2652C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646758 | |||||||
chr2:17646865 | G | A | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-2545G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17646865 | |||||||
chr2:17647020 | T | C | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163-2390T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647020 | |||||||
chr2:17647072 | T | C | 1 | a0001c0001t0005g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.163-2338T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647072 | |||||||
chr2:17647177 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0003g0086 a0001c0001t0003g0103 |
3 | HG01109.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.163-2233G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647177 | |||||||
chr2:17647344 | G | A | 1 | a0001c0001t0013g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163-2066G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647344 | |||||||
chr2:17647379 | G | C | 1 | a0001c0001t0019g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.163-2031G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647379 | |||||||
chr2:17647416 | C | T | 131 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(128): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.163-1994C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647416 | |||||||
chr2:17647610 | T | C | 1 | a0001c0001t0021g0191 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.163-1800T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647610 | |||||||
chr2:17647769 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.163-1641T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647769 | |||||||
chr2:17647847 | T | C | 13 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0016g0041 others(10): Show |
13 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-1563T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17647847 | |||||||
chr2:17648182 | T | C | 1 | a0001c0001t0014g0214 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.163-1228T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648182 | |||||||
chr2:17648214 | C | T | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.163-1196C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648214 | |||||||
chr2:17648332 | A | C | 1 | a0001c0001t0004g0024 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.163-1078A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648332 | |||||||
chr2:17648761 | C | A | 3 | a0001c0001t0003g0085 a0001c0001t0003g0086 a0001c0001t0003g0103 |
3 | HG01109.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.163-649C>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648761 | |||||||
chr2:17648864 | A | G | 3 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0076 |
3 | HG02559.hp2 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.163-546A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648864 | |||||||
chr2:17648890 | T | C | 1 | a0001c0001t0009g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.163-520T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648890 | |||||||
chr2:17648993 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0014 |
3 | HG00408.hp2 HG00438.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.163-417G>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17648993 | |||||||
chr2:17649070 | G | A | 1 | a0001c0001t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163-340G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17649070 | |||||||
chr2:17649142 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.163-268T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17649142 | |||||||
chr2:17649332 | T | G | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(9): Show |
12 | HG02056.hp1 HG02129.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-78T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 2/3 | chr2 | 17649332 | |||||||
chr2:17649644 | T | C | 1 | a0001c0001t0007g0204 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.378+19T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649644 | |||||||
chr2:17649724 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+99G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649724 | |||||||
chr2:17649746 | C | T | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.378+121C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649746 | |||||||
chr2:17649920 | T | G | 2 | a0001c0001t0021g0090 a0001c0001t0021g0091 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.378+295T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649920 | |||||||
chr2:17649933 | G | A | 1 | a0001c0001t0030g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.378+308G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649933 | |||||||
chr2:17649962 | G | A | 1 | a0001c0001t0012g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.378+337G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17649962 | |||||||
chr2:17650050 | G | A | 1 | a0001c0001t0031g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.378+425G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650050 | |||||||
chr2:17650351 | C | T | 170 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(167): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.378+726C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650351 | |||||||
chr2:17650427 | C | T | 2 | a0001c0001t0010g0116 a0001c0001t0010g0126 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.378+802C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650427 | |||||||
chr2:17650791 | T | G | 11 | a0001c0001t0016g0041 a0001c0001t0016g0153 a0001c0001t0016g0161 others(8): Show |
11 | HG00639.hp2 HG02451.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+1166T>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17650791 | |||||||
chr2:17651261 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.378+1636G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17651261 | |||||||
chr2:17651659 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.378+2034C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17651659 | |||||||
chr2:17651706 | TTC | T | 3 | a0001c0001t0010g0116 a0001c0001t0010g0126 a0001c0001t0019g0195 |
3 | HG02572.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.378+2085_378+2086d others(4): Show |
VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 17651706 | ||||||
chr2:17652120 | A | G | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.378+2495A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652120 | |||||||
chr2:17652207 | TC | T | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.378+2584delC | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 17652207 | ||||||
chr2:17652209 | C | G | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.378+2584C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652209 | |||||||
chr2:17652316 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.378+2691G>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652316 | |||||||
chr2:17652372 | T | C | 105 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(102): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.378+2747T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652372 | |||||||
chr2:17652688 | A | G | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379-2509A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17652688 | |||||||
chr2:17653185 | C | T | 100 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(97): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.379-2012C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653185 | |||||||
chr2:17653348 | T | A | 8 | a0001c0001t0007g0196 a0001c0001t0007g0198 a0001c0001t0007g0202 others(5): Show |
8 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-1849T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653348 | |||||||
chr2:17653391 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.379-1806C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653391 | |||||||
chr2:17653434 | C | T | 2 | a0001c0001t0008g0114 a0001c0001t0008g0115 |
2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.379-1763C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653434 | |||||||
chr2:17653487 | T | C | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.379-1710T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653487 | |||||||
chr2:17653603 | T | C | 1 | a0001c0001t0003g0111 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.379-1594T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653603 | |||||||
chr2:17653636 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.379-1561C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653636 | |||||||
chr2:17653782 | A | C | 85 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(82): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.379-1415A>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653782 | |||||||
chr2:17653797 | C | G | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.379-1400C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653797 | |||||||
chr2:17653828 | T | A | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.379-1369T>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653828 | |||||||
chr2:17653991 | C | T | 6 | a0001c0001t0020g0008 a0001c0001t0020g0117 a0001c0001t0020g0200 others(3): Show |
8 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.379-1206C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653991 | |||||||
chr2:17653992 | A | G | 83 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0003g0075 others(80): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.379-1205A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17653992 | |||||||
chr2:17654022 | A | G | 1 | a0001c0001t0015g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379-1175A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654022 | |||||||
chr2:17654115 | G | A | 1 | a0001c0001t0005g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.379-1082G>A | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654115 | |||||||
chr2:17654368 | A | G | 9 | a0001c0001t0010g0077 a0001c0001t0010g0078 a0001c0001t0010g0079 others(6): Show |
9 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-829A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654368 | |||||||
chr2:17654456 | A | G | 1 | a0001c0001t0009g0050 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.379-741A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654456 | |||||||
chr2:17654507 | T | C | 22 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(19): Show |
22 | HG00140.hp2 HG01069.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-690T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654507 | |||||||
chr2:17654626 | C | T | 1 | a0001c0001t0010g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-571C>T | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654626 | |||||||
chr2:17654788 | A | G | 3 | a0001c0001t0013g0071 a0001c0001t0013g0072 a0001c0001t0013g0073 |
3 | HG01192.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.379-409A>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654788 | |||||||
chr2:17654794 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0007g0196 |
2 | HG01261.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.379-403C>G | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654794 | |||||||
chr2:17654953 | T | C | 2 | a0001c0001t0021g0191 a0001c0001t0021g0192 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.379-244T>C | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | chr2 | 17654953 | |||||||
chr2:17655183 | C | CT | 25 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0168 others(22): Show |
25 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.379-8dupT | VSNL1 | ENSG00000163032.12 | transcript | ENST00000295156.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 17655183 |