Item | Value |
---|---|
geneid | 50488 |
ensemblid | ENSG00000141503.17 |
hgncid | 17565 |
symbol | MINK1 |
name | misshapen like kinase 1 |
refseq_nuc | NM_153827.5 |
refseq_prot | NP_722549.2 |
ensembl_nuc | ENST00000355280.11 |
ensembl_prot | ENSP00000347427.6 |
mane_status | MANE Select |
chr | chr17 |
start | 4833340 |
end | 4898061 |
strand | + |
ver | v1.2 |
region | chr17:4833340-4898061 |
region5000 | chr17:4828340-4903061 |
regionname0 | MINK1_chr17_4833340_4898061 |
regionname5000 | MINK1_chr17_4828340_4903061 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1332 | 196 | 71 | 37 | 70 | 8 | 9 | 54 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0002 | 1/0 | 1332 | 81 | 15 | 28 | 17 | 5 | 15 | 16 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0003 | 0/0 | 1332 | 68 | 1 | 6 | 45 | 1 | 15 | 33 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0004 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0005 | 0/0 | 1332 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0006 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0007 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0008 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0009 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0010 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(242): Show |
chr17 | 4828340 | 4903061 |
a0011 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1327): Show |
chr17 | 4828340 | 4903061 |
a0012 | 0/0 | 1337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | MGDPA others(1332): Show |
chr17 | 4828340 | 4903061 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3996 | 147 | 48 | 31 | 54 | 6 | 8 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0004 | 0/1 | 3996 | 24 | 1 | 4 | 16 | 2 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0005 | 0/0 | 3996 | 17 | 16 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0008 | 0/0 | 3996 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0011 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0014 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0017 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0001c0018 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0002c0002 | 1/0 | 3996 | 77 | 15 | 24 | 17 | 5 | 15 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0002c0010 | 0/0 | 3996 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0002c0012 | 0/0 | 3996 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0003c0003 | 0/0 | 3996 | 63 | 1 | 6 | 40 | 1 | 15 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0003c0007 | 0/0 | 3996 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0003c0013 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0003c0020 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0004c0006 | 0/0 | 3996 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0005c0009 | 0/0 | 3996 | 2 | 0 | 1 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0005c0023 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0006c0021 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0006c0025 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0007c0022 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0008c0015 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0009c0019 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0010c0026 | 0/0 | 4120 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(4115): Show |
chr17 | 4828340 | 4903061 | ||
a0011c0016 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(3991): Show |
chr17 | 4828340 | 4903061 | ||
a0012c0024 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | ATGGG others(4006): Show |
chr17 | 4828340 | 4903061 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5020 | 42 | 6 | 14 | 16 | 2 | 4 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0003 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0004 | 0/0 | 5020 | 7 | 6 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0005 | 0/0 | 5020 | 20 | 5 | 9 | 6 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0007 | 0/0 | 5020 | 14 | 0 | 4 | 6 | 3 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0008 | 0/0 | 5017 | 4 | 2 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0009 | 0/0 | 5020 | 10 | 8 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0012 | 0/0 | 5020 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0013 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0014 | 0/0 | 5020 | 3 | 2 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0016 | 0/0 | 5020 | 4 | 4 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0017 | 0/0 | 5020 | 5 | 0 | 0 | 5 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0018 | 0/0 | 5017 | 4 | 2 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0020 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0021 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0023 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0024 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0025 | 0/0 | 5017 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0029 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0030 | 0/0 | 5017 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0031 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0032 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0043 | 0/0 | 5017 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0046 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0047 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0048 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0050 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0051 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0052 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0055 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0001t0056 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0004t0006 | 0/0 | 5017 | 16 | 1 | 2 | 12 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0004t0016 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0004t0019 | 0/1 | 5020 | 4 | 0 | 2 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0004t0027 | 0/0 | 5017 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0004t0042 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0002 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0006 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0008 | 0/0 | 5017 | 8 | 8 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0012 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0022 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0037 | 0/0 | 5017 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0049 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0005t0054 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0008t0002 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0011t0006 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0011t0041 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0001c0014t0009 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0017t0002 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0001c0018t0004 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0001 | 0/0 | 5020 | 48 | 4 | 18 | 9 | 5 | 12 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0002 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0004 | 0/0 | 5020 | 13 | 10 | 3 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0014 | 0/0 | 5020 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0015 | 0/0 | 5020 | 5 | 0 | 2 | 0 | 0 | 3 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0020 | 0/0 | 5020 | 3 | 0 | 1 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0035 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0040 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0002c0002t0045 | 1/0 | 5017 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0002c0010t0015 | 0/0 | 5020 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0012t0001 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0002c0012t0004 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0003 | 0/0 | 5020 | 33 | 1 | 2 | 18 | 1 | 11 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0010 | 0/0 | 5017 | 9 | 0 | 3 | 4 | 0 | 2 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0011 | 0/0 | 5020 | 7 | 0 | 0 | 6 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0013 | 0/0 | 5020 | 6 | 0 | 0 | 6 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0026 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0028 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0033 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0034 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0036 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0038 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0003t0039 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5012): Show |
chr17 | 4828340 | 4903061 |
a0003c0007t0003 | 0/0 | 5020 | 3 | 0 | 0 | 3 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0013t0003 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0003c0020t0011 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0004c0006t0012 | 0/0 | 5020 | 4 | 0 | 0 | 4 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0005c0009t0044 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0005c0009t0053 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0005c0023t0009 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0006c0021t0007 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0006c0025t0005 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0007c0022t0004 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0008c0015t0002 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0009c0019t0001 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0010c0026t0003 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5139): Show |
chr17 | 4828340 | 4903061 |
a0011c0016t0028 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5015): Show |
chr17 | 4828340 | 4903061 |
a0012c0024t0006 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | AGTGC others(5027): Show |
chr17 | 4828340 | 4903061 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0009g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0014g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0017g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0018g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0021g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0021g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0023g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0023g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0024g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0024g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0024g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0025g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0025g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0025g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0029g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0029g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0030g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0030g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0031g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0032g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0043g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0046g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0047g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0048g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0050g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0051g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0052g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0055g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0001t0056g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0016g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0331 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0019g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0027g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0027g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0004t0042g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0012g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0022g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0037g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0049g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0005t0054g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0008t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0008t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0008t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0011t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0011t0041g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0014t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0017t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0001c0018t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0014g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0015g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0020g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0020g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0020g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0035g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0040g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0002t0045g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0010t0015g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0010t0015g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0012t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0002c0012t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0010g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0026g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0028g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0033g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0034g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0036g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0038g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0003t0039g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0007t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0007t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0013t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0003c0020t0011g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0004c0006t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0005c0009t0044g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0005c0009t0053g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0005c0023t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0006c0021t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0006c0025t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0007c0022t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0008c0015t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0009c0019t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0010c0026t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0011c0016t0028g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
a0012c0024t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0299 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0294 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0274 | EUR | GBR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0106 | EUR | FIN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00280 | hp2 | a0003 | c0003 | t0003 | g0007 | EUR | FIN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00423 | hp1 | a0003 | c0003 | t0011 | g0028 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00438 | hp1 | a0003 | c0003 | t0010 | g0015 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00438 | hp2 | a0001 | c0001 | t0012 | g0098 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00544 | hp2 | a0003 | c0003 | t0010 | g0066 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00558 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00558 | hp2 | a0003 | c0003 | t0013 | g0077 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00609 | hp1 | a0001 | c0004 | t0006 | g0338 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00609 | hp2 | a0003 | c0003 | t0003 | g0036 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00621 | hp1 | a0001 | c0004 | t0006 | g0348 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00621 | hp2 | a0004 | c0006 | t0012 | g0120 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00639 | hp2 | a0003 | c0003 | t0010 | g0040 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0323 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00642 | hp2 | a0001 | c0005 | t0037 | g0059 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00673 | hp1 | a0001 | c0004 | t0006 | g0329 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00673 | hp2 | a0001 | c0001 | t0050 | g0133 | EAS | CHS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00733 | hp1 | a0002 | c0002 | t0004 | g0277 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0315 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00738 | hp2 | a0002 | c0012 | t0001 | g0153 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG00741 | hp2 | a0002 | c0002 | t0015 | g0295 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0321 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01069 | hp2 | a0001 | c0004 | t0006 | g0344 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0319 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01074 | hp1 | a0001 | c0004 | t0006 | g0345 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01074 | hp2 | a0001 | c0001 | t0032 | g0194 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01099 | hp1 | a0002 | c0002 | t0020 | g0318 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01099 | hp2 | a0002 | c0010 | t0015 | g0303 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01106 | hp2 | a0002 | c0010 | t0015 | g0297 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0279 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0166 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01167 | hp1 | a0005 | c0009 | t0053 | g0208 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0217 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0325 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0316 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01192 | hp1 | a0001 | c0004 | t0019 | g0349 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01243 | hp1 | a0001 | c0001 | t0043 | g0160 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01243 | hp2 | a0001 | c0018 | t0004 | g0334 | AMR | PUR | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01256 | hp1 | a0003 | c0003 | t0003 | g0045 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01256 | hp2 | a0002 | c0002 | t0004 | g0267 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01257 | hp2 | a0002 | c0002 | t0015 | g0271 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01258 | hp1 | a0002 | c0002 | t0004 | g0268 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01261 | hp2 | a0003 | c0003 | t0010 | g0067 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0084 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01346 | hp2 | a0003 | c0003 | t0010 | g0032 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0101 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01361 | hp2 | a0003 | c0003 | t0003 | g0038 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0108 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0107 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0302 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01517 | hp1 | a0001 | c0004 | t0019 | g0343 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0086 | EUR | IBS | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01884 | hp2 | a0001 | c0005 | t0054 | g0210 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01891 | hp1 | a0001 | c0005 | t0008 | g0232 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01891 | hp2 | a0001 | c0001 | t0009 | g0205 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01928 | hp2 | a0001 | c0001 | t0007 | g0105 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0317 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0113 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02027 | hp2 | a0001 | c0001 | t0030 | g0099 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02055 | hp2 | a0001 | c0001 | t0023 | g0244 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02083 | hp1 | a0003 | c0003 | t0003 | g0009 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02083 | hp2 | a0001 | c0001 | t0008 | g0103 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02129 | hp1 | a0003 | c0003 | t0011 | g0044 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02129 | hp2 | a0001 | c0001 | t0029 | g0179 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02132 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02132 | hp2 | a0003 | c0003 | t0003 | g0050 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02135 | hp1 | a0003 | c0007 | t0003 | g0002 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0275 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02145 | hp2 | a0001 | c0005 | t0022 | g0149 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02148 | hp2 | a0001 | c0004 | t0019 | g0333 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02155 | hp1 | a0001 | c0001 | t0017 | g0115 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02155 | hp2 | a0003 | c0003 | t0003 | g0027 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02165 | hp1 | a0003 | c0003 | t0039 | g0078 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02165 | hp2 | a0003 | c0003 | t0013 | g0065 | EAS | CDX | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0247 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02257 | hp2 | a0001 | c0001 | t0055 | g0199 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02258 | hp2 | a0007 | c0022 | t0004 | g0146 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0097 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02280 | hp2 | a0002 | c0002 | t0004 | g0144 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0112 | AMR | PEL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02451 | hp1 | a0001 | c0001 | t0016 | g0226 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02523 | hp2 | a0001 | c0001 | t0018 | g0100 | EAS | KHV | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02572 | hp2 | a0001 | c0011 | t0041 | g0347 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02602 | hp2 | a0003 | c0003 | t0010 | g0014 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02615 | hp1 | a0001 | c0005 | t0008 | g0230 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02615 | hp2 | a0001 | c0008 | t0002 | g0158 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02622 | hp1 | a0001 | c0001 | t0021 | g0079 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02622 | hp2 | a0001 | c0005 | t0008 | g0242 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02630 | hp2 | a0001 | c0005 | t0006 | g0233 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0278 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0056 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0326 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02717 | hp1 | a0001 | c0008 | t0002 | g0157 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02717 | hp2 | a0001 | c0001 | t0046 | g0198 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02723 | hp1 | a0006 | c0021 | t0007 | g0220 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0285 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0104 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02735 | hp2 | a0003 | c0003 | t0003 | g0051 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0140 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02818 | hp1 | a0001 | c0001 | t0016 | g0223 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02886 | hp1 | a0001 | c0001 | t0024 | g0246 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02886 | hp2 | a0001 | c0005 | t0012 | g0150 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02895 | hp1 | a0001 | c0005 | t0008 | g0228 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02897 | hp1 | a0001 | c0005 | t0008 | g0229 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02922 | hp1 | a0001 | c0005 | t0008 | g0227 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0215 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02965 | hp1 | a0001 | c0001 | t0021 | g0080 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02965 | hp2 | a0001 | c0005 | t0022 | g0221 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0041 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03017 | hp2 | a0002 | c0002 | t0015 | g0296 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03041 | hp1 | a0001 | c0005 | t0049 | g0241 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03041 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0314 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0219 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03130 | hp1 | a0001 | c0001 | t0021 | g0081 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0212 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03195 | hp2 | a0008 | c0015 | t0002 | g0167 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03209 | hp1 | a0001 | c0001 | t0016 | g0225 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03209 | hp2 | a0001 | c0005 | t0022 | g0151 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03239 | hp1 | a0001 | c0001 | t0047 | g0130 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0269 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0224 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03453 | hp2 | a0001 | c0011 | t0006 | g0335 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0204 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0264 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03491 | hp2 | a0003 | c0003 | t0003 | g0033 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03492 | hp2 | a0003 | c0003 | t0003 | g0048 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03516 | hp1 | a0001 | c0005 | t0008 | g0243 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0216 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03579 | hp1 | a0002 | c0002 | t0004 | g0239 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03579 | hp2 | a0002 | c0002 | t0040 | g0143 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0306 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0042 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0328 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03704 | hp2 | a0003 | c0003 | t0011 | g0062 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03710 | hp1 | a0001 | c0001 | t0048 | g0095 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0072 | SAS | PJL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0324 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03831 | hp2 | a0003 | c0003 | t0003 | g0039 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03834 | hp1 | a0002 | c0002 | t0015 | g0276 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03834 | hp2 | a0003 | c0003 | t0003 | g0046 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0270 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03942 | hp1 | a0001 | c0017 | t0002 | g0195 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03942 | hp2 | a0009 | c0019 | t0001 | g0260 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04184 | hp1 | a0002 | c0002 | t0015 | g0286 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04184 | hp2 | a0003 | c0003 | t0010 | g0029 | SAS | BEB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0047 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0305 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG04204 | hp2 | a0003 | c0003 | t0036 | g0034 | SAS | STU | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18522 | hp1 | a0001 | c0001 | t0018 | g0259 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18522 | hp2 | a0002 | c0002 | t0004 | g0142 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0257 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18906 | hp2 | a0001 | c0001 | t0014 | g0253 | AFR | YRI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18940 | hp2 | a0003 | c0003 | t0011 | g0018 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18942 | hp1 | a0003 | c0003 | t0013 | g0055 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18943 | hp1 | a0001 | c0001 | t0007 | g0093 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18943 | hp2 | a0003 | c0003 | t0011 | g0068 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0053 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18944 | hp2 | a0001 | c0004 | t0006 | g0337 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18947 | hp1 | a0003 | c0003 | t0013 | g0043 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18947 | hp2 | a0001 | c0001 | t0013 | g0075 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18948 | hp2 | a0001 | c0001 | t0031 | g0087 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18949 | hp1 | a0001 | c0001 | t0012 | g0096 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18949 | hp2 | a0003 | c0007 | t0003 | g0002 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18950 | hp1 | a0002 | c0002 | t0014 | g0308 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18950 | hp2 | a0001 | c0001 | t0018 | g0172 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18951 | hp1 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18951 | hp2 | a0001 | c0001 | t0029 | g0131 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18954 | hp1 | a0001 | c0004 | t0016 | g0352 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18954 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18961 | hp2 | a0001 | c0001 | t0017 | g0091 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18962 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18962 | hp2 | a0003 | c0013 | t0003 | g0057 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18964 | hp2 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18966 | hp1 | a0004 | c0006 | t0012 | g0102 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18966 | hp2 | a0003 | c0020 | t0011 | g0023 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18967 | hp1 | a0003 | c0003 | t0026 | g0082 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18968 | hp1 | a0001 | c0004 | t0006 | g0136 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18968 | hp2 | a0001 | c0004 | t0027 | g0074 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18969 | hp1 | a0004 | c0006 | t0012 | g0114 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18969 | hp2 | a0002 | c0002 | t0014 | g0289 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18970 | hp1 | a0001 | c0001 | t0025 | g0138 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18971 | hp1 | a0001 | c0001 | t0025 | g0132 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18973 | hp1 | a0004 | c0006 | t0012 | g0090 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18973 | hp2 | a0001 | c0004 | t0042 | g0346 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18975 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18975 | hp2 | a0001 | c0004 | t0006 | g0350 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18979 | hp1 | a0001 | c0004 | t0006 | g0135 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18979 | hp2 | a0003 | c0003 | t0003 | g0011 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18980 | hp1 | a0003 | c0003 | t0003 | g0073 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18980 | hp2 | a0001 | c0004 | t0006 | g0332 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18983 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18983 | hp2 | a0003 | c0007 | t0003 | g0061 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18988 | hp1 | a0001 | c0004 | t0006 | g0351 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18988 | hp2 | a0002 | c0002 | t0020 | g0288 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18989 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18990 | hp1 | a0005 | c0009 | t0044 | g0124 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18990 | hp2 | a0003 | c0003 | t0034 | g0025 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18994 | hp1 | a0010 | c0026 | t0003 | g0076 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18995 | hp1 | a0011 | c0016 | t0028 | g0016 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18995 | hp2 | a0001 | c0001 | t0030 | g0085 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18998 | hp1 | a0003 | c0003 | t0003 | g0035 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18999 | hp1 | a0003 | c0003 | t0003 | g0054 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA18999 | hp2 | a0001 | c0001 | t0012 | g0110 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19000 | hp1 | a0001 | c0001 | t0017 | g0128 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19000 | hp2 | a0003 | c0003 | t0033 | g0020 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19004 | hp1 | a0001 | c0001 | t0052 | g0134 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19005 | hp1 | a0001 | c0004 | t0027 | g0060 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19010 | hp1 | a0002 | c0002 | t0014 | g0290 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19010 | hp2 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19011 | hp1 | a0001 | c0001 | t0007 | g0117 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19012 | hp2 | a0002 | c0002 | t0035 | g0071 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19030 | hp1 | a0001 | c0014 | t0009 | g0206 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19030 | hp2 | a0005 | c0023 | t0009 | g0353 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19043 | hp1 | a0001 | c0001 | t0051 | g0207 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19043 | hp2 | a0001 | c0005 | t0008 | g0231 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19057 | hp2 | a0001 | c0004 | t0006 | g0339 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19063 | hp1 | a0003 | c0003 | t0011 | g0019 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19064 | hp1 | a0003 | c0003 | t0003 | g0037 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19065 | hp1 | a0003 | c0003 | t0013 | g0052 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19065 | hp2 | a0001 | c0001 | t0025 | g0139 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19066 | hp2 | a0002 | c0002 | t0014 | g0312 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19070 | hp1 | a0003 | c0003 | t0003 | g0026 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19070 | hp2 | a0001 | c0001 | t0031 | g0123 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19074 | hp1 | a0003 | c0003 | t0010 | g0008 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19074 | hp2 | a0002 | c0002 | t0020 | g0301 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19077 | hp2 | a0003 | c0003 | t0010 | g0031 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0024 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19081 | hp2 | a0003 | c0003 | t0011 | g0021 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19084 | hp1 | a0003 | c0003 | t0013 | g0058 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19085 | hp1 | a0001 | c0004 | t0006 | g0340 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19085 | hp2 | a0003 | c0003 | t0028 | g0017 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19087 | hp1 | a0001 | c0004 | t0006 | g0336 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19090 | hp1 | a0012 | c0024 | t0006 | g0330 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19090 | hp2 | a0003 | c0003 | t0026 | g0013 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0064 | EAS | JPT | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0322 | AFR | ASW | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20129 | hp2 | a0001 | c0001 | t0023 | g0245 | AFR | ASW | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0261 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20805 | hp1 | a0001 | c0004 | t0006 | g0342 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20805 | hp2 | a0001 | c0001 | t0056 | g0258 | EUR | TSI | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20905 | hp1 | a0003 | c0003 | t0003 | g0012 | SAS | GIH | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | GIH | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01123 | hp1 | a0003 | c0003 | t0038 | g0022 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG01123 | hp2 | a0002 | c0012 | t0004 | g0190 | AMR | CLM | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02109 | hp1 | a0003 | c0003 | t0003 | g0030 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02486 | hp1 | a0001 | c0001 | t0020 | g0148 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02559 | hp1 | a0002 | c0002 | t0004 | g0145 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG02559 | hp2 | a0002 | c0002 | t0004 | g0266 | AFR | ACB | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG03471 | hp2 | a0001 | c0001 | t0024 | g0209 | AFR | MSL | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG06807 | hp1 | a0001 | c0005 | t0002 | g0152 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20300 | hp1 | a0001 | c0008 | t0002 | g0156 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA20300 | hp2 | a0001 | c0004 | t0006 | g0341 | AFR | USA | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA21309 | hp1 | a0006 | c0025 | t0005 | g0147 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
NA21309 | hp2 | a0002 | c0002 | t0004 | g0141 | AFR | LWK | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
homoSapiens | chm13v2 | a0001 | c0004 | t0019 | g0331 | REF | REF | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
homoSapiens | grch38p0 | a0002 | c0002 | t0045 | g0234 | REF | REF | MINK1_chr17_4828340_4903061 | MINK1 | chr17 | 4828340 | 4903061 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4887670 | A | ACAGCAGC others(8): Show |
1 | a0012 | 1 | NA19090.hp1 | disruptive_inframe_insertion | MODERATE | c.1124_1138dupTGCAGC others(9): Show |
p.Leu375_Gln379dup | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/32 | 1383/5017 | 1139/3999 | 380/1332 | INFO_REALIGN_3_PRIME | chr17 | 4887670 | ||
chr17:4891691 | G | A | 1 | a0004 | 4 | HG00621.hp2 NA18966.hp1 NA18969.hp1 others(1): Show |
missense_variant | MODERATE | c.1976G>A | p.Arg659His | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/32 | 2220/5017 | 1976/3999 | 659/1332 | chr17 | 4891691 | |||
chr17:4891716 | G | T | 1 | a0007 | 1 | HG02258.hp2 | missense_variant&splice_region_variant | MODERATE | c.2001G>T | p.Lys667Asn | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/32 | 2245/5017 | 2001/3999 | 667/1332 | chr17 | 4891716 | |||
chr17:4892427 | A | C | 1 | a0006 | 2 | HG02723.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2113A>C | p.Ile705Leu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 18/32 | 2357/5017 | 2113/3999 | 705/1332 | chr17 | 4892427 | |||
chr17:4892979 | T | C | 9 | a0001 a0003 a0004 others(6): Show |
276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
missense_variant&splice_region_variant | MODERATE | c.2312T>C | p.Val771Ala | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/32 | 2556/5017 | 2312/3999 | 771/1332 | chr17 | 4892979 | |||
chr17:4892991 | C | T | 8 | a0001 a0003 a0004 others(5): Show |
273 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
missense_variant | MODERATE | c.2324C>T | p.Pro775Leu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/32 | 2568/5017 | 2324/3999 | 775/1332 | chr17 | 4892991 | |||
chr17:4893535 | G | C | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.2502G>C | p.Glu834Asp | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/32 | 2746/5017 | 2502/3999 | 834/1332 | chr17 | 4893535 | |||
chr17:4894010 | G | A | 3 | a0003 a0010 a0011 |
70 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
missense_variant | MODERATE | c.2587G>A | p.Val863Ile | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 22/32 | 2831/5017 | 2587/3999 | 863/1332 | chr17 | 4894010 | |||
chr17:4894532 | C | A | 1 | a0011 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.2816C>A | p.Ser939Tyr | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/32 | 3060/5017 | 2816/3999 | 939/1332 | chr17 | 4894532 | |||
chr17:4894615 | G | A | 1 | a0009 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2899G>A | p.Asp967Asn | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/32 | 3143/5017 | 2899/3999 | 967/1332 | chr17 | 4894615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4833589 | C | T | 1 | a0001c0008 | 3 | HG02615.hp2 HG02717.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.6C>T | p.Gly2Gly | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/32 | 250/5017 | 6/3999 | 2/1332 | chr17 | 4833589 | |||
chr17:4884425 | C | T | 1 | a0002c0012 | 2 | HG00738.hp2 HG01123.hp2 |
synonymous_variant | LOW | c.369C>T | p.Asn123Asn | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/32 | 613/5017 | 369/3999 | 123/1332 | chr17 | 4884425 | |||
chr17:4884983 | G | A | 1 | a0003c0013 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.489G>A | p.Glu163Glu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 6/32 | 733/5017 | 489/3999 | 163/1332 | chr17 | 4884983 | |||
chr17:4887658 | A | G | 2 | a0001c0005 a0006c0025 |
18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.1098A>G | p.Ser366Ser | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/32 | 1342/5017 | 1098/3999 | 366/1332 | chr17 | 4887658 | |||
chr17:4889757 | C | T | 4 | a0001c0004 a0001c0011 a0005c0023 others(1): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
synonymous_variant | LOW | c.1341C>T | p.Arg447Arg | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/32 | 1585/5017 | 1341/3999 | 447/1332 | chr17 | 4889757 | |||
chr17:4891097 | G | A | 1 | a0001c0014 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1713G>A | p.Pro571Pro | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/32 | 1957/5017 | 1713/3999 | 571/1332 | chr17 | 4891097 | |||
chr17:4892761 | C | T | 1 | a0003c0020 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.2304C>T | p.Arg768Arg | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/32 | 2548/5017 | 2304/3999 | 768/1332 | chr17 | 4892761 | |||
chr17:4894066 | C | T | 2 | a0003c0007 a0010c0026 |
4 | HG02135.hp1 NA18949.hp2 NA18983.hp2 others(1): Show |
synonymous_variant | LOW | c.2643C>T | p.Tyr881Tyr | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 22/32 | 2887/5017 | 2643/3999 | 881/1332 | chr17 | 4894066 | |||
chr17:4894236 | C | T | 1 | a0001c0011 | 2 | HG02572.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.2733C>T | p.Asp911Asp | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/32 | 2977/5017 | 2733/3999 | 911/1332 | chr17 | 4894236 | |||
chr17:4895435 | G | A | 1 | a0001c0017 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.3171G>A | p.Arg1057Arg | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/32 | 3415/5017 | 3171/3999 | 1057/1332 | chr17 | 4895435 | |||
chr17:4896028 | G | A | 1 | a0002c0010 | 2 | HG01099.hp2 HG01106.hp2 |
synonymous_variant | LOW | c.3390G>A | p.Leu1130Leu | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 28/32 | 3634/5017 | 3390/3999 | 1130/1332 | chr17 | 4896028 | |||
chr17:4896521 | C | T | 1 | a0001c0018 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.3708C>T | p.Tyr1236Tyr | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 30/32 | 3952/5017 | 3708/3999 | 1236/1332 | chr17 | 4896521 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4833398 | G | C | 1 | a0001c0001t0032 | 1 | HG01074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-186G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/32 | 186 | chr17 | 4833398 | ||||||
chr17:4833543 | G | A | 22 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0021 others(19): Show |
79 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-41G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/32 | 41 | chr17 | 4833543 | ||||||
chr17:4897288 | C | T | 2 | a0001c0001t0056 a0003c0003t0039 |
2 | HG02165.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 1 | chr17 | 4897288 | ||||||
chr17:4897404 | C | G | 2 | a0001c0001t0055 a0001c0005t0054 |
2 | HG01884.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*117C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 117 | chr17 | 4897404 | ||||||
chr17:4897424 | G | A | 1 | a0002c0002t0040 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 137 | chr17 | 4897424 | ||||||
chr17:4897495 | G | C | 1 | a0003c0003t0033 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 208 | chr17 | 4897495 | ||||||
chr17:4897723 | A | G | 1 | a0005c0009t0053 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 436 | chr17 | 4897723 | ||||||
chr17:4897806 | A | C | 7 | a0001c0001t0009 a0001c0001t0025 a0001c0001t0050 others(4): Show |
18 | HG00673.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*519A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 519 | chr17 | 4897806 | ||||||
chr17:4897828 | G | A | 1 | a0001c0011t0041 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 541 | chr17 | 4897828 | ||||||
chr17:4897830 | C | G | 27 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(24): Show |
93 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 543 | chr17 | 4897830 | ||||||
chr17:4897833 | C | T | 1 | a0001c0001t0046 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 546 | chr17 | 4897833 | ||||||
chr17:4897860 | C | T | 1 | a0001c0005t0049 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 573 | chr17 | 4897860 | ||||||
chr17:4897868 | C | A | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0016 others(37): Show |
163 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*581C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 581 | chr17 | 4897868 | ||||||
chr17:4897899 | T | C | 39 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0014 others(36): Show |
155 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*612T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 612 | chr17 | 4897899 | ||||||
chr17:4897978 | T | TCTC | 69 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(66): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*693_*695dupTCC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 696 | INFO_REALIGN_3_PRIME | chr17 | 4897978 | |||||
chr17:4897991 | C | T | 56 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(53): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 704 | chr17 | 4897991 | ||||||
chr17:4897993 | A | C | 18 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0023 others(15): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 32/32 | 706 | chr17 | 4897993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4833732 | G | A | 1 | a0003c0003t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.57+92G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4833732 | |||||||
chr17:4833747 | T | C | 128 | a0001c0001t0002g0129 a0001c0001t0003g0063 a0001c0001t0005g0001 others(125): Show |
133 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.57+107T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4833747 | |||||||
chr17:4834151 | G | T | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+511G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834151 | |||||||
chr17:4834176 | G | A | 78 | a0001c0001t0003g0063 a0001c0001t0013g0075 a0001c0001t0021g0079 others(75): Show |
79 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+536G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834176 | |||||||
chr17:4834195 | T | C | 87 | a0001c0001t0002g0137 a0001c0001t0003g0063 a0001c0001t0013g0075 others(84): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.57+555T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834195 | |||||||
chr17:4834342 | TTC | T | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+706_57+707delCT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4834342 | ||||||
chr17:4834396 | A | G | 1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.57+756A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834396 | |||||||
chr17:4834422 | G | A | 7 | a0002c0002t0004g0140 a0002c0002t0004g0141 a0002c0002t0004g0142 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+782G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834422 | |||||||
chr17:4834619 | A | AT | 26 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(23): Show |
26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+982dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4834619 | ||||||
chr17:4834810 | G | A | 1 | a0001c0001t0008g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.57+1170G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834810 | |||||||
chr17:4834875 | G | C | 1 | a0003c0003t0003g0007 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.57+1235G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4834875 | |||||||
chr17:4835018 | C | T | 1 | a0001c0001t0047g0130 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.57+1378C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835018 | |||||||
chr17:4835614 | G | A | 50 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(47): Show |
54 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.57+1974G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835614 | |||||||
chr17:4835663 | C | T | 45 | a0001c0001t0018g0314 a0002c0002t0001g0005 a0002c0002t0001g0285 others(42): Show |
46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.57+2023C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835663 | |||||||
chr17:4835825 | G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+2185G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835825 | |||||||
chr17:4835866 | T | G | 150 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0154 others(147): Show |
155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.57+2226T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835866 | |||||||
chr17:4835925 | A | T | 9 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(6): Show |
9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+2285A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4835925 | |||||||
chr17:4836117 | T | A | 10 | a0001c0001t0016g0223 a0001c0001t0016g0224 a0001c0001t0016g0225 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+2477T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836117 | |||||||
chr17:4836401 | A | G | 1 | a0001c0001t0025g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.57+2761A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836401 | |||||||
chr17:4836795 | T | A | 11 | a0001c0001t0016g0223 a0001c0001t0016g0224 a0001c0001t0016g0225 others(8): Show |
11 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+3155T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836795 | |||||||
chr17:4836900 | G | A | 9 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(6): Show |
9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+3260G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836900 | |||||||
chr17:4836971 | G | A | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+3331G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836971 | |||||||
chr17:4836978 | G | A | 1 | a0003c0003t0010g0008 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.57+3338G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4836978 | |||||||
chr17:4837017 | T | TA | 9 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(6): Show |
9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+3387dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4837017 | ||||||
chr17:4837249 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.57+3609A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837249 | |||||||
chr17:4837332 | C | T | 2 | a0002c0002t0001g0283 a0002c0002t0001g0284 |
2 | HG00735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.57+3692C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837332 | |||||||
chr17:4837452 | G | T | 9 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(6): Show |
9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+3812G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837452 | |||||||
chr17:4837652 | A | G | 1 | a0003c0003t0039g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.57+4012A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837652 | |||||||
chr17:4837713 | C | G | 1 | a0001c0001t0025g0138 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.57+4073C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837713 | |||||||
chr17:4837745 | A | G | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+4105A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837745 | |||||||
chr17:4837801 | C | T | 2 | a0002c0002t0001g0328 a0005c0023t0009g0353 |
2 | HG03688.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.57+4161C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4837801 | |||||||
chr17:4838228 | C | T | 3 | a0001c0001t0002g0137 a0001c0004t0006g0135 a0001c0004t0006g0136 |
3 | NA18939.hp1 NA18968.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.57+4588C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838228 | |||||||
chr17:4838359 | A | G | 334 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(331): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.57+4719A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838359 | |||||||
chr17:4838423 | A | G | 26 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(23): Show |
26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+4783A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838423 | |||||||
chr17:4838479 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.57+4839C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838479 | |||||||
chr17:4838498 | G | A | 4 | a0001c0005t0002g0152 a0001c0005t0012g0150 a0001c0005t0022g0149 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+4858G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838498 | |||||||
chr17:4838509 | T | C | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+4869T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838509 | |||||||
chr17:4838622 | G | A | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+4982G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838622 | |||||||
chr17:4838690 | A | T | 1 | a0003c0003t0013g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.57+5050A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838690 | |||||||
chr17:4838817 | A | G | 86 | a0001c0001t0002g0255 a0001c0001t0002g0281 a0001c0001t0009g0279 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.57+5177A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838817 | |||||||
chr17:4838947 | C | CT | 24 | a0001c0004t0006g0332 a0001c0004t0006g0336 a0001c0004t0006g0337 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.57+5321dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4838947 | ||||||
chr17:4838966 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.57+5326C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838966 | |||||||
chr17:4838967 | G | A | 1 | a0001c0001t0007g0084 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.57+5327G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838967 | |||||||
chr17:4838975 | G | A | 1 | a0003c0003t0003g0009 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.57+5335G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838975 | |||||||
chr17:4838977 | A | T | 1 | a0003c0003t0003g0009 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.57+5337A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4838977 | |||||||
chr17:4839004 | C | T | 1 | a0001c0001t0021g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.57+5364C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839004 | |||||||
chr17:4839006 | C | T | 2 | a0001c0001t0021g0081 a0002c0002t0001g0327 |
2 | HG00423.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.57+5366C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839006 | |||||||
chr17:4839012 | T | C | 57 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(54): Show |
58 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.57+5372T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839012 | |||||||
chr17:4839036 | C | T | 2 | a0001c0005t0022g0221 a0006c0021t0007g0220 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+5396C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839036 | |||||||
chr17:4839037 | A | G | 1 | a0002c0002t0001g0326 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57+5397A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839037 | |||||||
chr17:4839083 | A | G | 50 | a0001c0001t0005g0001 a0001c0001t0005g0088 a0001c0001t0005g0089 others(47): Show |
54 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.57+5443A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839083 | |||||||
chr17:4839084 | T | C | 2 | a0002c0002t0001g0254 a0002c0012t0001g0153 |
2 | HG00738.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.57+5444T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839084 | |||||||
chr17:4839093 | G | A | 1 | a0002c0012t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.57+5453G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839093 | |||||||
chr17:4839155 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+5515G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839155 | |||||||
chr17:4839164 | T | C | 4 | a0001c0001t0002g0155 a0001c0008t0002g0156 a0001c0008t0002g0157 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+5524T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839164 | |||||||
chr17:4839165 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.57+5525G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839165 | |||||||
chr17:4839189 | C | T | 2 | a0001c0004t0006g0351 a0001c0004t0016g0352 |
2 | NA18954.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.57+5549C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839189 | |||||||
chr17:4839195 | A | G | 2 | a0001c0005t0006g0233 a0001c0005t0008g0232 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.57+5555A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839195 | |||||||
chr17:4839235 | G | A | 4 | a0001c0001t0016g0223 a0001c0001t0016g0224 a0001c0001t0016g0225 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+5595G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839235 | |||||||
chr17:4839338 | T | A | 1 | a0001c0001t0030g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.57+5698T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839338 | |||||||
chr17:4839397 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.57+5757C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839397 | |||||||
chr17:4839649 | A | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+6009A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839649 | |||||||
chr17:4839659 | A | G | 1 | a0003c0003t0003g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.57+6019A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839659 | |||||||
chr17:4839680 | A | G | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.57+6040A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839680 | |||||||
chr17:4839934 | T | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+6294T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4839934 | |||||||
chr17:4839935 | ATTAATGT others(3): Show |
A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+6297_57+6306del others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839935 | ||||||
chr17:4839939 | A | ATATGTGT others(3): Show |
1 | a0001c0001t0025g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.57+6300_57+6301ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | A | ATG | 6 | a0001c0001t0005g0237 a0001c0001t0005g0238 a0001c0004t0006g0135 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+6344_57+6345dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | A | ATGTG | 3 | a0001c0001t0002g0137 a0001c0001t0025g0138 a0001c0001t0029g0131 |
3 | NA18939.hp1 NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.57+6342_57+6345dup others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0025g0132 a0001c0001t0052g0134 |
2 | NA18971.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.57+6336_57+6345dup others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATG | A | 60 | a0001c0001t0002g0187 a0001c0001t0002g0281 a0001c0001t0009g0214 others(57): Show |
61 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.57+6344_57+6345del others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTG | A | 17 | a0001c0001t0005g0211 a0001c0001t0009g0204 a0001c0001t0009g0205 others(14): Show |
17 | HG01891.hp2 HG02523.hp2 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.57+6342_57+6345del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTG | A | 20 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(17): Show |
20 | HG00099.hp2 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+6340_57+6345del others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTGT others(1): Show |
A | 22 | a0001c0001t0002g0222 a0001c0001t0007g0084 a0001c0001t0007g0117 others(19): Show |
22 | HG01167.hp1 HG01346.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.57+6338_57+6345del others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTGT others(3): Show |
A | 97 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0154 others(94): Show |
102 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.57+6336_57+6345del others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0002g0192 a0001c0001t0005g0097 a0001c0001t0020g0148 others(1): Show |
4 | HG02135.hp2 HG02273.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+6334_57+6345del others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0002g0178 a0003c0003t0026g0013 a0006c0025t0005g0147 |
3 | HG03491.hp1 NA19090.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.57+6332_57+6345del others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTGT others(13): Show |
A | 75 | a0001c0001t0003g0063 a0001c0001t0021g0079 a0001c0001t0021g0080 others(72): Show |
76 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+6326_57+6345del others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4839939 | ATGTGTGT others(17): Show |
A | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+6322_57+6345del others(24): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4839939 | ||||||
chr17:4840040 | A | T | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+6400A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840040 | |||||||
chr17:4840093 | A | G | 1 | a0001c0004t0006g0350 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.57+6453A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840093 | |||||||
chr17:4840224 | G | C | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+6584G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840224 | |||||||
chr17:4840299 | A | G | 4 | a0002c0002t0035g0071 a0003c0003t0003g0069 a0003c0003t0003g0070 others(1): Show |
4 | HG03710.hp2 NA18951.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+6659A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840299 | |||||||
chr17:4840477 | G | T | 1 | a0002c0002t0001g0325 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.57+6837G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840477 | |||||||
chr17:4840507 | G | GA | 28 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(25): Show |
28 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+6867_57+6868ins others(1): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840507 | |||||||
chr17:4840599 | T | C | 2 | a0003c0003t0003g0069 a0003c0003t0003g0070 |
2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.57+6959T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840599 | |||||||
chr17:4840834 | A | G | 337 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(334): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.57+7194A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840834 | |||||||
chr17:4840963 | T | C | 1 | a0002c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.57+7323T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840963 | |||||||
chr17:4840963 | T | G | 1 | a0001c0001t0014g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.57+7323T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4840963 | |||||||
chr17:4841009 | C | T | 27 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+7369C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841009 | |||||||
chr17:4841093 | C | G | 260 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+7453C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841093 | |||||||
chr17:4841093 | C | T | 1 | a0003c0003t0011g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.57+7453C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841093 | |||||||
chr17:4841102 | C | T | 9 | a0001c0005t0008g0227 a0001c0005t0008g0228 a0001c0005t0008g0229 others(6): Show |
9 | HG01891.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+7462C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841102 | |||||||
chr17:4841103 | G | A | 1 | a0003c0003t0010g0008 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.57+7463G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841103 | |||||||
chr17:4841128 | A | C | 27 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+7488A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841128 | |||||||
chr17:4841365 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+7725G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841365 | |||||||
chr17:4841388 | A | G | 3 | a0001c0001t0002g0281 a0002c0002t0001g0280 a0002c0002t0001g0324 |
3 | HG00738.hp1 HG01433.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.57+7748A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841388 | |||||||
chr17:4841522 | C | T | 9 | a0001c0005t0008g0227 a0001c0005t0008g0228 a0001c0005t0008g0229 others(6): Show |
9 | HG01891.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+7882C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841522 | |||||||
chr17:4841526 | C | G | 2 | a0001c0005t0022g0221 a0006c0021t0007g0220 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+7886C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841526 | |||||||
chr17:4841528 | T | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.57+7888T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841528 | |||||||
chr17:4841531 | G | A | 1 | a0003c0003t0003g0010 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.57+7891G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841531 | |||||||
chr17:4841942 | C | T | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.57+8302C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841942 | |||||||
chr17:4841947 | C | G | 10 | a0002c0002t0001g0005 a0002c0002t0001g0315 a0002c0002t0001g0316 others(7): Show |
11 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+8307C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4841947 | |||||||
chr17:4842076 | T | C | 2 | a0001c0001t0014g0159 a0001c0001t0043g0160 |
2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.57+8436T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842076 | |||||||
chr17:4842080 | C | T | 7 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(4): Show |
7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+8440C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842080 | |||||||
chr17:4842164 | T | C | 2 | a0001c0005t0012g0150 a0001c0005t0022g0149 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.57+8524T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842164 | |||||||
chr17:4842179 | A | G | 27 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+8539A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842179 | |||||||
chr17:4842202 | C | T | 6 | a0001c0001t0046g0198 a0001c0001t0055g0199 a0001c0004t0006g0348 others(3): Show |
6 | HG00621.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+8562C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842202 | |||||||
chr17:4842204 | A | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+8564A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842204 | |||||||
chr17:4842210 | C | T | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+8570C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842210 | |||||||
chr17:4842222 | C | CA | 160 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0154 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.57+8597dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4842222 | ||||||
chr17:4842222 | C | CAA | 24 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0163 others(21): Show |
24 | HG00423.hp2 HG00735.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.57+8596_57+8597dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4842222 | ||||||
chr17:4842309 | C | T | 1 | a0001c0001t0009g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.57+8669C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842309 | |||||||
chr17:4842318 | G | A | 1 | a0001c0001t0051g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+8678G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842318 | |||||||
chr17:4842321 | G | C | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+8681G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842321 | |||||||
chr17:4842692 | G | C | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+9052G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842692 | |||||||
chr17:4842905 | C | A | 1 | a0005c0009t0053g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.57+9265C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842905 | |||||||
chr17:4842999 | A | G | 27 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+9359A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4842999 | |||||||
chr17:4843062 | C | T | 1 | a0001c0001t0018g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57+9422C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843062 | |||||||
chr17:4843129 | A | T | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+9489A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843129 | |||||||
chr17:4843146 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57+9506C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843146 | |||||||
chr17:4843186 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+9546G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843186 | |||||||
chr17:4843248 | A | G | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+9608A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843248 | |||||||
chr17:4843275 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+9635G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843275 | |||||||
chr17:4843457 | G | A | 78 | a0001c0001t0002g0255 a0001c0001t0002g0281 a0001c0001t0009g0279 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.57+9817G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843457 | |||||||
chr17:4843463 | A | G | 1 | a0002c0002t0001g0291 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.57+9823A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843463 | |||||||
chr17:4843473 | G | A | 2 | a0001c0001t0007g0093 a0001c0001t0014g0092 |
2 | NA18943.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.57+9833G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843473 | |||||||
chr17:4843488 | GAAAGAA | G | 8 | a0001c0001t0002g0161 a0001c0001t0002g0165 a0001c0001t0002g0168 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+9864_57+9869del others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4843488 | ||||||
chr17:4843600 | T | A | 1 | a0001c0005t0049g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+9960T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843600 | |||||||
chr17:4843601 | G | A | 1 | a0001c0005t0049g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+9961G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843601 | |||||||
chr17:4843602 | C | T | 1 | a0001c0005t0049g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.57+9962C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843602 | |||||||
chr17:4843728 | T | C | 27 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+10088T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843728 | |||||||
chr17:4843872 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+10232G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843872 | |||||||
chr17:4843885 | C | G | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+10245C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843885 | |||||||
chr17:4843893 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+10253A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4843893 | |||||||
chr17:4844048 | G | A | 2 | a0001c0005t0022g0221 a0006c0021t0007g0220 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+10408G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844048 | |||||||
chr17:4844334 | G | A | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+10694G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844334 | |||||||
chr17:4844595 | G | A | 1 | a0001c0001t0024g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.57+10955G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844595 | |||||||
chr17:4844841 | G | T | 7 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(4): Show |
7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+11201G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844841 | |||||||
chr17:4844844 | T | G | 75 | a0001c0001t0003g0063 a0001c0004t0006g0135 a0001c0004t0006g0136 others(72): Show |
76 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+11204T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844844 | |||||||
chr17:4844875 | C | G | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+11235C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4844875 | |||||||
chr17:4845129 | G | A | 1 | a0002c0002t0004g0257 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.57+11489G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845129 | |||||||
chr17:4845155 | T | G | 1 | a0002c0002t0001g0283 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.57+11515T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845155 | |||||||
chr17:4845287 | G | C | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+11647G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845287 | |||||||
chr17:4845409 | G | C | 1 | a0001c0001t0005g0094 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.57+11769G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845409 | |||||||
chr17:4845638 | A | AT | 15 | a0001c0001t0005g0240 a0001c0001t0017g0128 a0001c0001t0025g0132 others(12): Show |
15 | HG00438.hp1 HG00673.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.57+12013dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4845638 | ||||||
chr17:4845676 | C | T | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.57+12036C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845676 | |||||||
chr17:4845721 | C | G | 1 | a0001c0004t0006g0348 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.57+12081C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845721 | |||||||
chr17:4845730 | G | A | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+12090G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845730 | |||||||
chr17:4845773 | T | C | 10 | a0001c0001t0002g0137 a0001c0001t0021g0079 a0001c0001t0021g0080 others(7): Show |
10 | HG00673.hp2 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+12133T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845773 | |||||||
chr17:4845803 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+12163G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845803 | |||||||
chr17:4845887 | C | T | 7 | a0001c0001t0002g0161 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+12247C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845887 | |||||||
chr17:4845893 | T | C | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+12253T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845893 | |||||||
chr17:4845911 | A | G | 170 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.57+12271A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845911 | |||||||
chr17:4845945 | T | G | 4 | a0003c0003t0010g0008 a0003c0003t0010g0066 a0003c0003t0028g0017 others(1): Show |
4 | HG00544.hp2 NA18995.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+12305T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845945 | |||||||
chr17:4845950 | T | G | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+12310T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4845950 | |||||||
chr17:4846000 | C | T | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | NA18967.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.57+12360C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846000 | |||||||
chr17:4846239 | G | A | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+12599G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846239 | |||||||
chr17:4846379 | A | C | 1 | a0003c0003t0013g0065 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.57+12739A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846379 | |||||||
chr17:4846535 | T | C | 81 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(78): Show |
82 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.57+12895T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846535 | |||||||
chr17:4846558 | CATCCTT | C | 75 | a0001c0001t0003g0063 a0001c0004t0006g0135 a0001c0004t0006g0136 others(72): Show |
76 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+12920_57+12925d others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4846558 | ||||||
chr17:4846610 | G | A | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.57+12970G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846610 | |||||||
chr17:4846641 | T | C | 81 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(78): Show |
82 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.57+13001T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846641 | |||||||
chr17:4846712 | C | G | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+13072C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846712 | |||||||
chr17:4846728 | C | T | 4 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(1): Show |
4 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+13088C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846728 | |||||||
chr17:4846794 | C | G | 3 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 |
3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+13154C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846794 | |||||||
chr17:4846926 | G | A | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.57+13286G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4846926 | |||||||
chr17:4847138 | A | G | 7 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(4): Show |
7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+13498A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847138 | |||||||
chr17:4847230 | G | GTTCA | 71 | a0001c0001t0002g0165 a0001c0001t0002g0168 a0001c0001t0002g0169 others(68): Show |
72 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.57+13623_57+13626d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4847230 | ||||||
chr17:4847230 | G | GTTCATTC others(1): Show |
6 | a0001c0001t0003g0063 a0001c0001t0021g0079 a0001c0001t0021g0080 others(3): Show |
6 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+13619_57+13626d others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4847230 | ||||||
chr17:4847230 | GTTCA | G | 28 | a0001c0001t0002g0255 a0001c0001t0005g0211 a0001c0001t0009g0204 others(25): Show |
28 | HG01168.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+13623_57+13626d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4847230 | ||||||
chr17:4847278 | G | A | 74 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0018g0259 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.57+13638G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847278 | |||||||
chr17:4847588 | G | A | 4 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0001g0294 others(1): Show |
4 | HG00140.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+13948G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847588 | |||||||
chr17:4847752 | G | A | 1 | a0005c0009t0053g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.57+14112G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4847752 | |||||||
chr17:4848180 | A | G | 4 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 others(1): Show |
4 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+14540A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848180 | |||||||
chr17:4848225 | A | G | 3 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 |
3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+14585A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848225 | |||||||
chr17:4848523 | G | A | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.57+14883G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848523 | |||||||
chr17:4848621 | A | G | 5 | a0001c0004t0027g0060 a0003c0003t0011g0062 a0003c0007t0003g0002 others(2): Show |
6 | HG02135.hp1 HG03704.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+14981A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848621 | |||||||
chr17:4848650 | G | A | 74 | a0001c0001t0003g0063 a0001c0004t0006g0135 a0001c0004t0006g0136 others(71): Show |
75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.57+15010G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848650 | |||||||
chr17:4848965 | G | A | 78 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0016g0223 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.57+15325G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848965 | |||||||
chr17:4848999 | CT | C | 7 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(4): Show |
7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+15360delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4848999 | |||||||
chr17:4849058 | A | ATGGCTGA others(11): Show |
1 | a0005c0009t0044g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.57+15421_57+15438d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4849058 | ||||||
chr17:4849137 | C | G | 78 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0016g0223 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.57+15497C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849137 | |||||||
chr17:4849170 | A | G | 1 | a0002c0002t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.57+15530A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849170 | |||||||
chr17:4849210 | C | T | 4 | a0001c0005t0002g0152 a0001c0005t0012g0150 a0001c0005t0022g0149 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+15570C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849210 | |||||||
chr17:4849323 | C | T | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+15683C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849323 | |||||||
chr17:4849496 | C | G | 1 | a0002c0002t0001g0313 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+15856C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849496 | |||||||
chr17:4849508 | T | C | 7 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(4): Show |
7 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+15868T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849508 | |||||||
chr17:4849540 | GCTAACTC others(4): Show |
G | 3 | a0001c0001t0002g0197 a0001c0001t0032g0194 a0001c0017t0002g0195 |
3 | HG01074.hp2 HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.57+15903_57+15913d others(13): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4849540 | ||||||
chr17:4849619 | C | T | 1 | a0003c0003t0003g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.57+15979C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849619 | |||||||
chr17:4849665 | T | C | 1 | a0003c0003t0011g0028 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.57+16025T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849665 | |||||||
chr17:4849675 | G | A | 13 | a0001c0001t0005g0211 a0001c0001t0009g0204 a0001c0001t0009g0205 others(10): Show |
13 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+16035G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849675 | |||||||
chr17:4849784 | G | C | 1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.57+16144G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849784 | |||||||
chr17:4849895 | C | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+16255C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849895 | |||||||
chr17:4849981 | C | T | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+16341C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4849981 | |||||||
chr17:4850015 | T | A | 1 | a0003c0003t0010g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+16375T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850015 | |||||||
chr17:4850188 | C | T | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+16548C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850188 | |||||||
chr17:4850190 | AGCAAT | A | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+16553_57+16557d others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4850190 | ||||||
chr17:4850364 | A | C | 1 | a0001c0001t0031g0123 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.57+16724A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850364 | |||||||
chr17:4850439 | A | G | 21 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(18): Show |
21 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.57+16799A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850439 | |||||||
chr17:4850519 | G | C | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+16879G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850519 | |||||||
chr17:4850519 | G | GC | 138 | a0001c0001t0002g0004 a0001c0001t0002g0161 a0001c0001t0002g0162 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.57+16887dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4850519 | ||||||
chr17:4850528 | G | A | 1 | a0001c0005t0022g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+16888G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4850528 | |||||||
chr17:4851023 | C | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+17383C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851023 | |||||||
chr17:4851345 | A | C | 194 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.57+17705A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851345 | |||||||
chr17:4851417 | T | G | 1 | a0001c0005t0008g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57+17777T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851417 | |||||||
chr17:4851499 | C | T | 12 | a0001c0001t0005g0211 a0001c0001t0009g0204 a0001c0001t0009g0205 others(9): Show |
12 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+17859C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851499 | |||||||
chr17:4851541 | A | G | 1 | a0003c0003t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.57+17901A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851541 | |||||||
chr17:4851566 | T | C | 1 | a0001c0001t0056g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.57+17926T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851566 | |||||||
chr17:4851603 | T | C | 31 | a0001c0001t0002g0137 a0001c0001t0004g0248 a0001c0001t0004g0249 others(28): Show |
31 | HG00673.hp2 HG01167.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+17963T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851603 | |||||||
chr17:4851732 | G | A | 159 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.57+18092G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851732 | |||||||
chr17:4851953 | T | C | 1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.57+18313T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4851953 | |||||||
chr17:4851999 | C | CA | 21 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(18): Show |
21 | HG00438.hp2 HG01358.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+18387dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4851999 | C | CAAA | 6 | a0001c0001t0004g0248 a0001c0005t0006g0233 a0001c0005t0008g0242 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+18385_57+18387d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4851999 | C | CAAAA | 9 | a0001c0001t0002g0255 a0001c0005t0002g0152 a0001c0005t0008g0227 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+18384_57+18387d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4851999 | C | CAAAAAAA | 6 | a0001c0001t0009g0204 a0001c0001t0009g0212 a0001c0001t0009g0213 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+18381_57+18387d others(9): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4851999 | CA | C | 58 | a0001c0001t0003g0063 a0001c0001t0005g0238 a0001c0001t0007g0122 others(55): Show |
59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.57+18387delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4851999 | CAA | C | 14 | a0001c0001t0002g0155 a0001c0001t0002g0171 a0001c0001t0002g0173 others(11): Show |
15 | HG00735.hp1 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+18386_57+18387d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4851999 | CAAA | C | 150 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0161 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.57+18385_57+18387d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4851999 | ||||||
chr17:4852023 | A | C | 138 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.57+18383A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852023 | |||||||
chr17:4852082 | G | A | 1 | a0001c0001t0009g0212 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+18442G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852082 | |||||||
chr17:4852129 | A | G | 108 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(105): Show |
109 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.57+18489A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852129 | |||||||
chr17:4852630 | C | G | 1 | a0001c0001t0004g0249 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+18990C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852630 | |||||||
chr17:4852754 | G | A | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+19114G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852754 | |||||||
chr17:4852769 | T | TGGGGGAG others(466): Show |
1 | a0001c0005t0002g0152 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(475): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(450): Show |
1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(459): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(467): Show |
28 | a0001c0001t0002g0255 a0001c0001t0009g0204 a0001c0001t0009g0205 others(25): Show |
28 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(476): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(612): Show |
5 | a0001c0004t0006g0344 a0001c0004t0006g0345 a0001c0004t0019g0333 others(2): Show |
5 | HG01069.hp2 HG01074.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(621): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(503): Show |
1 | a0004c0006t0012g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(512): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(451): Show |
1 | a0001c0001t0002g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(460): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(555): Show |
1 | a0003c0003t0003g0037 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(553): Show |
1 | a0009c0019t0001g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(562): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(555): Show |
1 | a0001c0001t0025g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(538): Show |
8 | a0001c0001t0002g0137 a0001c0001t0025g0138 a0001c0001t0025g0139 others(5): Show |
8 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(554): Show |
9 | a0001c0001t0020g0148 a0002c0002t0001g0005 a0002c0002t0001g0315 others(6): Show |
10 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(563): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(535): Show |
2 | a0003c0003t0003g0038 a0003c0003t0010g0067 |
2 | HG01261.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(544): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(549): Show |
1 | a0001c0001t0004g0248 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(558): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(553): Show |
1 | a0001c0001t0007g0126 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(562): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(503): Show |
1 | a0001c0001t0008g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(512): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(521): Show |
44 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(41): Show |
48 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(457): Show |
1 | a0001c0001t0008g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(466): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(607): Show |
1 | a0002c0002t0004g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(616): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(538): Show |
17 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(14): Show |
17 | HG01358.hp2 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(555): Show |
1 | a0001c0001t0004g0249 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(534): Show |
2 | a0001c0005t0022g0221 a0006c0021t0007g0220 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(543): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(537): Show |
62 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0024g0209 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(572): Show |
3 | a0001c0001t0016g0223 a0001c0001t0016g0224 a0001c0001t0016g0225 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(581): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(538): Show |
2 | a0002c0002t0001g0316 a0002c0002t0001g0323 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(521): Show |
1 | a0003c0003t0003g0039 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(554): Show |
1 | a0003c0003t0003g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(563): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(521): Show |
2 | a0003c0003t0010g0032 a0003c0003t0010g0040 |
2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(538): Show |
64 | a0001c0001t0003g0063 a0001c0001t0023g0244 a0001c0001t0023g0245 others(61): Show |
65 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(520): Show |
1 | a0003c0003t0003g0035 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(529): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(538): Show |
1 | a0003c0013t0003g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(547): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(504): Show |
1 | a0001c0001t0007g0101 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(513): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(555): Show |
1 | a0001c0001t0016g0226 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(564): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(520): Show |
3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(529): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(521): Show |
2 | a0002c0002t0035g0071 a0003c0003t0010g0008 |
2 | NA19012.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(530): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(537): Show |
1 | a0002c0002t0001g0274 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(642): Show |
1 | a0003c0003t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(651): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(572): Show |
2 | a0001c0001t0018g0259 a0001c0001t0018g0314 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.57+19144_57+19145i others(581): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(448): Show |
7 | a0001c0001t0002g0162 a0001c0001t0002g0170 a0001c0001t0002g0171 others(4): Show |
7 | NA18940.hp1 NA18950.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(457): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(451): Show |
1 | a0001c0001t0002g0177 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(460): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(452): Show |
42 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(39): Show |
43 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.57+19144_57+19145i others(461): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852769 | T | TGGGGGAG others(522): Show |
1 | a0001c0001t0048g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.57+19144_57+19145i others(531): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852769 | ||||||
chr17:4852776 | G | GTGTGGTT others(537): Show |
1 | a0002c0002t0001g0325 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.57+19144_57+19145i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852776 | ||||||
chr17:4852785 | A | G | 23 | a0001c0001t0007g0122 a0001c0004t0006g0329 a0001c0004t0006g0332 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+19145A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852785 | |||||||
chr17:4852790 | T | G | 23 | a0001c0001t0007g0122 a0001c0004t0006g0329 a0001c0004t0006g0332 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+19150T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852790 | |||||||
chr17:4852798 | G | GA | 4 | a0001c0001t0007g0122 a0001c0008t0002g0156 a0001c0008t0002g0157 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+19158_57+19159i others(3): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852798 | |||||||
chr17:4852799 | T | A | 19 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.57+19159T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852799 | |||||||
chr17:4852802 | G | GTGGGGGA others(537): Show |
1 | a0001c0001t0007g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.57+19162_57+19163i others(546): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852802 | |||||||
chr17:4852802 | G | GTGGGGGA others(468): Show |
3 | a0001c0008t0002g0156 a0001c0008t0002g0157 a0001c0008t0002g0158 |
3 | HG02615.hp2 HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.57+19162_57+19163i others(477): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852802 | |||||||
chr17:4852802 | G | T | 19 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.57+19162G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852802 | |||||||
chr17:4852816 | G | GTTGGTGG others(578): Show |
1 | a0001c0018t0004g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.57+19178_57+19179i others(587): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | ||||||
chr17:4852816 | G | GTTGGTGG others(578): Show |
16 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(13): Show |
16 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+19178_57+19179i others(587): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | ||||||
chr17:4852816 | G | GTTGGTGG others(595): Show |
1 | a0001c0004t0006g0342 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.57+19178_57+19179i others(604): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | ||||||
chr17:4852816 | G | GTTGGTGG others(595): Show |
1 | a0001c0004t0042g0346 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.57+19178_57+19179i others(604): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852816 | ||||||
chr17:4852819 | T | G | 24 | a0001c0001t0007g0122 a0001c0001t0020g0148 a0001c0004t0006g0329 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19179T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852819 | |||||||
chr17:4852833 | GTT | G | 7 | a0001c0001t0007g0086 a0001c0001t0007g0101 a0001c0001t0007g0104 others(4): Show |
7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19194_57+19195d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852833 | |||||||
chr17:4852836 | G | C | 7 | a0001c0001t0007g0086 a0001c0001t0007g0101 a0001c0001t0007g0104 others(4): Show |
7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19196G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852836 | |||||||
chr17:4852836 | G | T | 19 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.57+19196G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852836 | |||||||
chr17:4852837 | G | C | 7 | a0001c0001t0007g0086 a0001c0001t0007g0101 a0001c0001t0007g0104 others(4): Show |
7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+19197G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852837 | |||||||
chr17:4852884 | A | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19244A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852884 | |||||||
chr17:4852887 | T | G | 26 | a0001c0001t0046g0198 a0001c0001t0055g0199 a0001c0004t0006g0329 others(23): Show |
26 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.57+19247T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852887 | |||||||
chr17:4852901 | G | A | 5 | a0001c0004t0006g0344 a0001c0004t0006g0345 a0001c0004t0019g0333 others(2): Show |
5 | HG01069.hp2 HG01074.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+19261G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852901 | |||||||
chr17:4852904 | G | GGTGGGGG others(10): Show |
19 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.57+19277_57+19278i others(19): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4852904 | ||||||
chr17:4852904 | G | T | 5 | a0001c0004t0006g0344 a0001c0004t0006g0345 a0001c0004t0019g0333 others(2): Show |
5 | HG01069.hp2 HG01074.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+19264G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4852904 | |||||||
chr17:4853012 | G | A | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.57+19372G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853012 | |||||||
chr17:4853076 | A | ATGGGGGG others(11): Show |
1 | a0003c0003t0003g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+19443_57+19460d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853076 | ||||||
chr17:4853089 | G | A | 1 | a0003c0003t0010g0032 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.57+19449G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853089 | |||||||
chr17:4853123 | T | TTGGGGGA others(10): Show |
3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+19483_57+19484i others(19): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853123 | |||||||
chr17:4853124 | G | GGGAGTGT others(7): Show |
1 | a0001c0001t0005g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+19486_57+19487i others(16): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853124 | ||||||
chr17:4853124 | G | GGGGGGAG others(10): Show |
306 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(303): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.57+19517_57+19533d others(19): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853124 | ||||||
chr17:4853124 | G | T | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+19484G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853124 | |||||||
chr17:4853132 | T | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+19492T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853132 | |||||||
chr17:4853173 | G | GGTGGGGG others(28): Show |
23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+19533_57+19534i others(37): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853173 | |||||||
chr17:4853174 | A | G | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+19534A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853174 | |||||||
chr17:4853174 | A | T | 1 | a0001c0011t0041g0347 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+19534A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853174 | |||||||
chr17:4853205 | TTGG | T | 4 | a0001c0004t0027g0060 a0003c0007t0003g0002 a0003c0007t0003g0061 others(1): Show |
5 | HG02135.hp1 NA18949.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+19569_57+19571d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853205 | ||||||
chr17:4853213 | G | A | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+19573G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853213 | |||||||
chr17:4853214 | G | A | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+19574G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853214 | |||||||
chr17:4853214 | G | GGAGTGTG others(11): Show |
1 | a0001c0011t0041g0347 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+19588_57+19589i others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853214 | ||||||
chr17:4853272 | G | T | 1 | a0001c0005t0022g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+19632G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853272 | |||||||
chr17:4853300 | GGAGTGTG others(11): Show |
G | 1 | a0001c0001t0002g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.57+19677_57+19694d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853300 | ||||||
chr17:4853352 | A | AAGAGTGT others(8): Show |
1 | a0001c0001t0008g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.57+19713_57+19727d others(17): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853352 | ||||||
chr17:4853368 | GGAGTGTG others(11): Show |
G | 2 | a0003c0003t0003g0041 a0003c0003t0003g0042 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.57+19741_57+19758d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4853368 | ||||||
chr17:4853423 | T | C | 51 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(48): Show |
55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.57+19783T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853423 | |||||||
chr17:4853500 | G | C | 76 | a0001c0001t0003g0063 a0001c0001t0023g0244 a0001c0001t0023g0245 others(73): Show |
77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.57+19860G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853500 | |||||||
chr17:4853620 | T | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.57+19980T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4853620 | |||||||
chr17:4854228 | C | G | 2 | a0002c0002t0001g0272 a0002c0002t0001g0273 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.57+20588C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854228 | |||||||
chr17:4854303 | T | C | 108 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(105): Show |
109 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.57+20663T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854303 | |||||||
chr17:4854434 | G | C | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+20794G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854434 | |||||||
chr17:4854482 | T | G | 84 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(81): Show |
85 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.57+20842T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854482 | |||||||
chr17:4854565 | G | C | 3 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 |
3 | HG02486.hp2 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.57+20925G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854565 | |||||||
chr17:4854566 | T | C | 71 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(68): Show |
72 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.57+20926T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854566 | |||||||
chr17:4854879 | C | A | 338 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(335): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.57+21239C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854879 | |||||||
chr17:4854949 | A | G | 84 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(81): Show |
85 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.57+21309A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4854949 | |||||||
chr17:4855023 | A | G | 1 | a0001c0018t0004g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.57+21383A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855023 | |||||||
chr17:4855190 | T | TAA | 72 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0056g0258 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.57+21563_57+21564d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855190 | ||||||
chr17:4855190 | TA | T | 27 | a0001c0001t0029g0131 a0001c0004t0006g0329 a0001c0004t0006g0332 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+21564delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855190 | ||||||
chr17:4855226 | C | G | 3 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 |
3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+21586C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855226 | |||||||
chr17:4855235 | C | T | 20 | a0001c0001t0056g0258 a0002c0002t0001g0254 a0002c0002t0001g0256 others(17): Show |
20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+21595C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855235 | |||||||
chr17:4855314 | G | A | 1 | a0001c0005t0008g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.57+21674G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855314 | |||||||
chr17:4855403 | G | A | 1 | a0002c0002t0015g0276 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.57+21763G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855403 | |||||||
chr17:4855485 | C | CA | 211 | a0001c0001t0002g0281 a0001c0001t0003g0063 a0001c0001t0004g0248 others(208): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.57+21860dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855485 | ||||||
chr17:4855485 | C | CAA | 113 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(110): Show |
114 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.57+21859_57+21860d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855485 | ||||||
chr17:4855485 | C | CAAA | 8 | a0001c0001t0002g0155 a0001c0001t0002g0170 a0001c0001t0002g0173 others(5): Show |
8 | HG00621.hp1 HG00741.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+21858_57+21860d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855485 | ||||||
chr17:4855504 | C | T | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+21864C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855504 | |||||||
chr17:4855505 | G | A | 1 | a0001c0005t0054g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.57+21865G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855505 | |||||||
chr17:4855553 | C | T | 83 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(80): Show |
84 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.57+21913C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855553 | |||||||
chr17:4855556 | G | A | 2 | a0001c0005t0022g0221 a0006c0021t0007g0220 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+21916G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855556 | |||||||
chr17:4855687 | G | A | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+22047G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855687 | |||||||
chr17:4855726 | C | T | 5 | a0001c0001t0007g0086 a0001c0001t0007g0101 a0001c0001t0007g0106 others(2): Show |
5 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+22086C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855726 | |||||||
chr17:4855752 | A | G | 3 | a0003c0003t0003g0007 a0003c0003t0003g0037 a0003c0003t0026g0082 |
3 | HG00280.hp2 NA18967.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.57+22112A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855752 | |||||||
chr17:4855769 | C | CA | 9 | a0001c0001t0002g0129 a0001c0001t0002g0193 a0001c0001t0007g0109 others(6): Show |
9 | HG00741.hp1 HG01993.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+22147dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855769 | ||||||
chr17:4855769 | C | CAA | 19 | a0001c0004t0006g0329 a0001c0004t0006g0337 a0001c0004t0006g0338 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.57+22146_57+22147d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4855769 | ||||||
chr17:4855784 | A | G | 2 | a0002c0002t0001g0272 a0002c0002t0001g0273 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.57+22144A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855784 | |||||||
chr17:4855785 | A | G | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+22145A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4855785 | |||||||
chr17:4856046 | G | C | 1 | a0002c0002t0001g0264 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.58-22271G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856046 | |||||||
chr17:4856048 | C | T | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-22269C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856048 | |||||||
chr17:4856429 | C | T | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-21888C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856429 | |||||||
chr17:4856436 | T | C | 1 | a0003c0003t0003g0035 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58-21881T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856436 | |||||||
chr17:4856491 | C | T | 2 | a0002c0002t0001g0305 a0002c0002t0001g0325 |
2 | HG01168.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.58-21826C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856491 | |||||||
chr17:4856510 | G | A | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-21807G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856510 | |||||||
chr17:4856564 | G | A | 2 | a0002c0002t0001g0283 a0002c0002t0001g0284 |
2 | HG00735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.58-21753G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856564 | |||||||
chr17:4856657 | C | G | 28 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(25): Show |
28 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.58-21660C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856657 | |||||||
chr17:4856736 | C | G | 74 | a0001c0001t0003g0063 a0001c0001t0007g0093 a0001c0001t0014g0092 others(71): Show |
75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.58-21581C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856736 | |||||||
chr17:4856837 | G | C | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-21480G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856837 | |||||||
chr17:4856891 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58-21426G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4856891 | |||||||
chr17:4857115 | C | T | 1 | a0001c0001t0018g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-21202C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857115 | |||||||
chr17:4857313 | A | G | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-21004A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857313 | |||||||
chr17:4857422 | T | C | 2 | a0001c0001t0008g0083 a0001c0001t0008g0125 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.58-20895T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857422 | |||||||
chr17:4857458 | G | GT | 151 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0162 others(148): Show |
151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.58-20833dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | ||||||
chr17:4857458 | G | GTT | 41 | a0001c0001t0002g0281 a0001c0001t0009g0204 a0001c0001t0009g0205 others(38): Show |
41 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-20834_58-20833d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | ||||||
chr17:4857458 | G | GTTT | 5 | a0001c0001t0018g0314 a0002c0002t0001g0005 a0002c0002t0001g0316 others(2): Show |
6 | HG00642.hp1 HG01175.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-20835_58-20833d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | ||||||
chr17:4857458 | GT | G | 9 | a0001c0005t0022g0221 a0002c0002t0004g0140 a0002c0002t0004g0141 others(6): Show |
9 | HG00558.hp2 HG02165.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-20833delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857458 | ||||||
chr17:4857670 | G | A | 1 | a0001c0001t0056g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.58-20647G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4857670 | |||||||
chr17:4857938 | GAACTT | G | 31 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(28): Show |
31 | HG00642.hp2 HG01168.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.58-20371_58-20367d others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4857938 | ||||||
chr17:4858045 | G | T | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-20272G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858045 | |||||||
chr17:4858100 | T | C | 44 | a0001c0004t0027g0060 a0002c0002t0035g0071 a0003c0003t0003g0006 others(41): Show |
45 | HG00280.hp2 HG00423.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.58-20217T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858100 | |||||||
chr17:4858180 | A | G | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-20137A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858180 | |||||||
chr17:4858296 | G | C | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-20021G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858296 | |||||||
chr17:4858467 | A | T | 139 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.58-19850A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858467 | |||||||
chr17:4858479 | A | AT | 12 | a0001c0001t0002g0129 a0001c0001t0005g0116 a0001c0001t0017g0128 others(9): Show |
12 | HG02293.hp2 HG02523.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-19823dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4858479 | ||||||
chr17:4858479 | A | T | 1 | a0002c0002t0001g0274 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.58-19838A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858479 | |||||||
chr17:4858479 | AT | A | 49 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(46): Show |
49 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.58-19823delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4858479 | ||||||
chr17:4858617 | C | T | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-19700C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858617 | |||||||
chr17:4858665 | T | C | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-19652T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858665 | |||||||
chr17:4858740 | A | C | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-19577A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858740 | |||||||
chr17:4858827 | G | A | 1 | a0002c0002t0001g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58-19490G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858827 | |||||||
chr17:4858963 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.58-19354G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858963 | |||||||
chr17:4858974 | C | G | 1 | a0002c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58-19343C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4858974 | |||||||
chr17:4858995 | AC | A | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-19319delC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4858995 | ||||||
chr17:4859077 | C | T | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-19240C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859077 | |||||||
chr17:4859586 | G | A | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-18731G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859586 | |||||||
chr17:4859769 | CAA | C | 11 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-18547_58-18546d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859769 | |||||||
chr17:4859788 | C | CA | 78 | a0001c0001t0004g0248 a0001c0001t0004g0251 a0001c0001t0004g0252 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.58-18502dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | C | CAA | 21 | a0001c0001t0002g0281 a0001c0001t0004g0249 a0001c0001t0004g0250 others(18): Show |
21 | HG00642.hp2 HG00673.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.58-18503_58-18502d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | C | CAAA | 8 | a0001c0001t0002g0137 a0001c0001t0004g0282 a0001c0001t0029g0131 others(5): Show |
8 | HG00673.hp1 HG03139.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-18504_58-18502d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | C | CAAAA | 9 | a0001c0004t0006g0332 a0001c0004t0006g0336 a0001c0004t0006g0341 others(6): Show |
9 | HG01074.hp1 NA18954.hp1 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-18505_58-18502d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | C | CAAAAA | 8 | a0001c0004t0006g0337 a0001c0004t0006g0338 a0001c0004t0006g0340 others(5): Show |
8 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-18506_58-18502d others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | CA | C | 59 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0161 others(56): Show |
60 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.58-18502delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | CAAAAAAA others(1): Show |
C | 69 | a0001c0001t0003g0063 a0001c0004t0027g0060 a0002c0002t0035g0071 others(66): Show |
70 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.58-18509_58-18502d others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859788 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0009g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58-18514_58-18502d others(15): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859788 | ||||||
chr17:4859863 | TA | T | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-18444delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4859863 | ||||||
chr17:4859903 | T | C | 1 | a0001c0001t0018g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-18414T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859903 | |||||||
chr17:4859911 | C | T | 1 | a0001c0001t0007g0108 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.58-18406C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4859911 | |||||||
chr17:4860031 | T | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-18286T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860031 | |||||||
chr17:4860256 | T | C | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-18061T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860256 | |||||||
chr17:4860312 | A | G | 1 | a0001c0005t0054g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58-18005A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860312 | |||||||
chr17:4860484 | TAATC | T | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-17830_58-17827d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4860484 | ||||||
chr17:4860732 | T | C | 2 | a0003c0003t0028g0017 a0011c0016t0028g0016 |
2 | NA18995.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.58-17585T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860732 | |||||||
chr17:4860946 | G | A | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-17371G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4860946 | |||||||
chr17:4861064 | C | T | 135 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.58-17253C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861064 | |||||||
chr17:4861257 | C | T | 1 | a0002c0002t0001g0321 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.58-17060C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861257 | |||||||
chr17:4861395 | G | A | 1 | a0001c0001t0029g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.58-16922G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861395 | |||||||
chr17:4861694 | T | G | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-16623T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861694 | |||||||
chr17:4861748 | G | A | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-16569G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861748 | |||||||
chr17:4861807 | A | G | 1 | a0001c0005t0008g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.58-16510A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861807 | |||||||
chr17:4861950 | T | C | 1 | a0001c0001t0005g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.58-16367T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4861950 | |||||||
chr17:4862168 | C | G | 28 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(25): Show |
28 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.58-16149C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862168 | |||||||
chr17:4862425 | C | T | 11 | a0001c0005t0006g0233 a0001c0005t0008g0227 a0001c0005t0008g0228 others(8): Show |
11 | HG00642.hp2 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-15892C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862425 | |||||||
chr17:4862465 | G | A | 1 | a0009c0019t0001g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.58-15852G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862465 | |||||||
chr17:4862470 | C | T | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-15847C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862470 | |||||||
chr17:4862506 | C | T | 192 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.58-15811C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862506 | |||||||
chr17:4862569 | G | A | 51 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(48): Show |
55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-15748G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862569 | |||||||
chr17:4862608 | T | C | 192 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.58-15709T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862608 | |||||||
chr17:4862611 | G | A | 51 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(48): Show |
55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-15706G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862611 | |||||||
chr17:4862653 | CA | C | 58 | a0001c0001t0002g0188 a0001c0001t0007g0109 a0001c0001t0009g0204 others(55): Show |
58 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.58-15651delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4862653 | ||||||
chr17:4862759 | G | A | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-15558G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862759 | |||||||
chr17:4862791 | T | C | 205 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.58-15526T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862791 | |||||||
chr17:4862849 | C | T | 53 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(50): Show |
53 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-15468C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862849 | |||||||
chr17:4862881 | A | C | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-15436A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862881 | |||||||
chr17:4862986 | A | G | 192 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.58-15331A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4862986 | |||||||
chr17:4863160 | A | G | 201 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.58-15157A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863160 | |||||||
chr17:4863245 | T | C | 42 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(39): Show |
42 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.58-15072T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863245 | |||||||
chr17:4863304 | C | G | 16 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(13): Show |
16 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-15013C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863304 | |||||||
chr17:4863334 | C | T | 5 | a0002c0002t0001g0304 a0002c0002t0001g0310 a0002c0002t0001g0327 others(2): Show |
5 | HG00423.hp2 NA18988.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-14983C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863334 | |||||||
chr17:4863509 | G | C | 72 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0056g0258 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.58-14808G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863509 | |||||||
chr17:4863598 | C | T | 75 | a0001c0001t0002g0178 a0001c0001t0002g0187 a0001c0001t0002g0222 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.58-14719C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863598 | |||||||
chr17:4863642 | T | C | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-14675T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863642 | |||||||
chr17:4863652 | A | G | 1 | a0001c0001t0017g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.58-14665A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4863652 | |||||||
chr17:4863780 | C | CATT | 156 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(153): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.58-14515_58-14513d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4863780 | ||||||
chr17:4863780 | C | CATTATT | 5 | a0001c0001t0016g0224 a0001c0001t0046g0198 a0001c0001t0055g0199 others(2): Show |
5 | HG01069.hp1 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-14518_58-14513d others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4863780 | ||||||
chr17:4864212 | C | T | 1 | a0002c0002t0001g0321 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.58-14105C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864212 | |||||||
chr17:4864213 | G | A | 4 | a0001c0001t0020g0148 a0001c0001t0024g0209 a0001c0001t0024g0219 others(1): Show |
4 | HG01167.hp1 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-14104G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864213 | |||||||
chr17:4864292 | G | C | 54 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(51): Show |
54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-14025G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864292 | |||||||
chr17:4864501 | G | A | 1 | a0002c0002t0015g0295 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58-13816G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864501 | |||||||
chr17:4864514 | T | C | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-13803T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864514 | |||||||
chr17:4864652 | G | A | 3 | a0002c0002t0001g0264 a0002c0002t0001g0269 a0002c0002t0001g0274 |
3 | HG00140.hp2 HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.58-13665G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864652 | |||||||
chr17:4864680 | G | A | 1 | a0001c0005t0054g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58-13637G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864680 | |||||||
chr17:4864680 | G | T | 133 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.58-13637G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864680 | |||||||
chr17:4864778 | C | T | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-13539C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864778 | |||||||
chr17:4864913 | C | G | 1 | a0003c0003t0039g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.58-13404C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4864913 | |||||||
chr17:4865001 | C | T | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58-13316C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865001 | |||||||
chr17:4865071 | C | G | 1 | a0002c0002t0001g0291 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.58-13246C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865071 | |||||||
chr17:4865082 | ATTTTTAT others(7): Show |
A | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-13223_58-13210d others(16): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865082 | ||||||
chr17:4865202 | G | A | 2 | a0002c0002t0001g0307 a0002c0002t0001g0311 |
2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.58-13115G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865202 | |||||||
chr17:4865272 | AAC | A | 54 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(51): Show |
54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-13039_58-13038d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865272 | ||||||
chr17:4865300 | G | C | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-13017G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865300 | |||||||
chr17:4865436 | A | AAAAT | 11 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(8): Show |
11 | HG00673.hp2 HG03710.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-12858_58-12855d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865436 | ||||||
chr17:4865472 | G | A | 2 | a0002c0002t0001g0307 a0002c0002t0001g0311 |
2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.58-12845G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865472 | |||||||
chr17:4865548 | C | A | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-12769C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865548 | |||||||
chr17:4865551 | C | G | 2 | a0002c0002t0004g0267 a0002c0002t0004g0268 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.58-12766C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865551 | |||||||
chr17:4865674 | G | T | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-12643G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865674 | |||||||
chr17:4865719 | C | CA | 27 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(24): Show |
27 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.58-12578dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | ||||||
chr17:4865719 | CA | C | 212 | a0001c0001t0002g0129 a0001c0001t0002g0137 a0001c0001t0002g0281 others(209): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.58-12578delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | ||||||
chr17:4865719 | CAA | C | 32 | a0001c0001t0002g0161 a0001c0001t0002g0176 a0001c0001t0013g0075 others(29): Show |
32 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.58-12579_58-12578d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | ||||||
chr17:4865719 | CAAA | C | 51 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(48): Show |
52 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.58-12580_58-12578d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865719 | ||||||
chr17:4865835 | C | T | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | NA18967.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.58-12482C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865835 | |||||||
chr17:4865879 | AGT | A | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-12436_58-12435d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4865879 | ||||||
chr17:4865942 | G | A | 5 | a0001c0005t0002g0152 a0001c0005t0012g0150 a0001c0005t0022g0149 others(2): Show |
5 | HG02145.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-12375G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4865942 | |||||||
chr17:4866123 | C | T | 39 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0162 others(36): Show |
40 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.58-12194C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866123 | |||||||
chr17:4866268 | C | G | 1 | a0001c0004t0006g0351 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.58-12049C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866268 | |||||||
chr17:4866471 | TA | T | 9 | a0001c0001t0008g0083 a0001c0001t0030g0085 a0001c0001t0030g0099 others(6): Show |
9 | HG01069.hp1 HG01081.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-11831delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866471 | ||||||
chr17:4866515 | G | A | 4 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0189 others(1): Show |
4 | HG00741.hp1 HG01070.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-11802G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866515 | |||||||
chr17:4866527 | T | C | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58-11790T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866527 | |||||||
chr17:4866609 | C | CA | 18 | a0001c0001t0005g0112 a0001c0001t0012g0096 a0001c0001t0012g0098 others(15): Show |
18 | HG00438.hp2 HG00673.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.58-11691dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866609 | ||||||
chr17:4866609 | CA | C | 59 | a0001c0001t0002g0176 a0001c0001t0009g0204 a0001c0001t0009g0205 others(56): Show |
59 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.58-11691delA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866609 | ||||||
chr17:4866609 | CAA | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.58-11692_58-11691d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4866609 | ||||||
chr17:4866659 | C | T | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-11658C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866659 | |||||||
chr17:4866796 | G | A | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.58-11521G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866796 | |||||||
chr17:4866799 | C | T | 51 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(48): Show |
55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-11518C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866799 | |||||||
chr17:4866849 | G | A | 3 | a0001c0008t0002g0156 a0001c0008t0002g0157 a0001c0008t0002g0158 |
3 | HG02615.hp2 HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.58-11468G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866849 | |||||||
chr17:4866859 | G | T | 1 | a0001c0004t0027g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.58-11458G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866859 | |||||||
chr17:4866902 | T | C | 45 | a0001c0001t0002g0281 a0002c0002t0001g0005 a0002c0002t0001g0280 others(42): Show |
46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.58-11415T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866902 | |||||||
chr17:4866929 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.58-11388C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4866929 | |||||||
chr17:4867074 | A | AAAT | 27 | a0001c0001t0002g0137 a0001c0001t0004g0249 a0001c0001t0004g0250 others(24): Show |
28 | HG00438.hp2 HG00621.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.58-11213_58-11211d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAAT | 52 | a0001c0001t0003g0063 a0001c0001t0018g0259 a0001c0001t0018g0314 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-11216_58-11211d others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(2): Show |
57 | a0001c0001t0002g0202 a0001c0001t0050g0133 a0001c0004t0006g0332 others(54): Show |
57 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.58-11219_58-11211d others(11): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(5): Show |
56 | a0001c0001t0002g0281 a0001c0001t0016g0223 a0001c0001t0016g0224 others(53): Show |
57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.58-11222_58-11211d others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(8): Show |
26 | a0001c0001t0002g0165 a0001c0001t0002g0168 a0001c0001t0002g0169 others(23): Show |
26 | HG00140.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.58-11225_58-11211d others(17): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(11): Show |
38 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(35): Show |
39 | HG00544.hp2 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.58-11228_58-11211d others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(14): Show |
19 | a0001c0001t0002g0164 a0001c0001t0002g0175 a0001c0001t0002g0183 others(16): Show |
19 | HG00099.hp1 HG01074.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-11231_58-11211d others(23): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(17): Show |
5 | a0001c0001t0002g0173 a0001c0001t0002g0185 a0001c0001t0005g0211 others(2): Show |
5 | HG01928.hp1 HG02004.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-11234_58-11211d others(26): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | AAATAATA others(20): Show |
3 | a0001c0001t0002g0178 a0001c0001t0002g0186 a0001c0001t0002g0188 |
3 | HG00639.hp1 HG02273.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.58-11237_58-11211d others(29): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867074 | ||||||
chr17:4867074 | A | ATAAT | 3 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 |
3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-11243_58-11242i others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867074 | |||||||
chr17:4867104 | T | TAATAATA others(11): Show |
3 | a0001c0001t0009g0216 a0001c0001t0009g0217 a0001c0014t0009g0206 |
3 | HG01168.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.58-11211_58-11210i others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867104 | ||||||
chr17:4867104 | T | TAATAATA others(14): Show |
2 | a0001c0001t0002g0200 a0001c0001t0009g0215 |
2 | HG01175.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.58-11211_58-11210i others(23): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867104 | ||||||
chr17:4867104 | T | TAATAATA others(17): Show |
1 | a0001c0001t0051g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-11211_58-11210i others(26): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867104 | ||||||
chr17:4867105 | A | AATAATAA others(13): Show |
1 | a0001c0001t0002g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.58-11211_58-11210i others(22): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867105 | ||||||
chr17:4867138 | G | GTT | 7 | a0001c0001t0005g0235 a0001c0001t0005g0237 a0001c0005t0008g0227 others(4): Show |
7 | HG00642.hp2 HG01358.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-11153_58-11152d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | ||||||
chr17:4867138 | G | GTTT | 13 | a0001c0001t0009g0212 a0001c0001t0009g0213 a0001c0001t0009g0215 others(10): Show |
13 | HG01168.hp1 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-11154_58-11152d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | ||||||
chr17:4867138 | G | GTTTT | 10 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0214 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-11155_58-11152d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | ||||||
chr17:4867138 | GTT | G | 80 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0161 others(77): Show |
81 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.58-11153_58-11152d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | ||||||
chr17:4867138 | GTTT | G | 216 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0162 others(213): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.58-11154_58-11152d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | ||||||
chr17:4867138 | GTTTT | G | 8 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(5): Show |
8 | HG00673.hp2 HG01993.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-11155_58-11152d others(6): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867138 | ||||||
chr17:4867147 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.58-11170T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867147 | |||||||
chr17:4867148 | T | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-11169T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867148 | |||||||
chr17:4867153 | T | G | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-11164T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867153 | |||||||
chr17:4867154 | T | G | 49 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(46): Show |
53 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.58-11163T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867154 | |||||||
chr17:4867158 | T | G | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-11159T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867158 | |||||||
chr17:4867388 | A | G | 1 | a0001c0001t0005g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58-10929A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867388 | |||||||
chr17:4867750 | G | A | 1 | a0003c0003t0010g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.58-10567G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867750 | |||||||
chr17:4867768 | C | T | 74 | a0001c0001t0003g0063 a0001c0004t0006g0135 a0001c0004t0006g0136 others(71): Show |
75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.58-10549C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867768 | |||||||
chr17:4867829 | G | T | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-10488G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867829 | |||||||
chr17:4867890 | A | G | 1 | a0001c0004t0006g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.58-10427A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4867890 | |||||||
chr17:4867971 | CT | C | 8 | a0001c0001t0002g0178 a0001c0001t0020g0148 a0001c0001t0024g0209 others(5): Show |
8 | HG01167.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-10331delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867971 | ||||||
chr17:4867971 | CTT | C | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.58-10332_58-10331d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4867971 | ||||||
chr17:4868125 | C | T | 133 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.58-10192C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868125 | |||||||
chr17:4868133 | C | T | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-10184C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868133 | |||||||
chr17:4868180 | T | C | 1 | a0003c0003t0011g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.58-10137T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868180 | |||||||
chr17:4868204 | T | C | 1 | a0001c0001t0007g0117 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.58-10113T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868204 | |||||||
chr17:4868252 | C | T | 2 | a0001c0001t0047g0130 a0001c0001t0048g0095 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.58-10065C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868252 | |||||||
chr17:4868256 | C | T | 34 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(31): Show |
34 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.58-10061C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868256 | |||||||
chr17:4868391 | C | T | 11 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-9926C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868391 | |||||||
chr17:4868431 | T | C | 1 | a0002c0002t0001g0313 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-9886T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868431 | |||||||
chr17:4868444 | C | T | 1 | a0003c0003t0010g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.58-9873C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868444 | |||||||
chr17:4868488 | A | G | 3 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 |
3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-9829A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868488 | |||||||
chr17:4868549 | A | G | 1 | a0001c0001t0051g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-9768A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868549 | |||||||
chr17:4868585 | C | G | 2 | a0001c0001t0009g0217 a0001c0014t0009g0206 |
2 | HG01168.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.58-9732C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868585 | |||||||
chr17:4868798 | C | T | 3 | a0002c0002t0001g0292 a0002c0002t0001g0293 a0002c0002t0001g0294 |
3 | HG00140.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58-9519C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868798 | |||||||
chr17:4868816 | G | A | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-9501G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868816 | |||||||
chr17:4868952 | C | G | 1 | a0001c0001t0008g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.58-9365C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4868952 | |||||||
chr17:4869033 | C | T | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-9284C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869033 | |||||||
chr17:4869084 | C | T | 1 | a0002c0002t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.58-9233C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869084 | |||||||
chr17:4869115 | G | A | 27 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.58-9202G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869115 | |||||||
chr17:4869219 | C | T | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-9098C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869219 | |||||||
chr17:4869242 | ATTATTAT others(4): Show |
A | 20 | a0001c0004t0006g0332 a0001c0004t0006g0336 a0001c0004t0006g0337 others(17): Show |
20 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-9069_58-9059del others(11): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869242 | ||||||
chr17:4869242 | ATTATTAT others(8): Show |
A | 3 | a0001c0004t0019g0333 a0001c0004t0019g0343 a0001c0018t0004g0334 |
3 | HG01243.hp2 HG01517.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.58-9069_58-9055del others(15): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869242 | ||||||
chr17:4869245 | A | ATTAT | 23 | a0001c0001t0005g0094 a0001c0001t0005g0118 a0001c0001t0007g0101 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.58-9029_58-9026dup others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | ||||||
chr17:4869245 | ATTAT | A | 30 | a0001c0001t0002g0137 a0001c0001t0004g0248 a0001c0001t0004g0282 others(27): Show |
30 | HG00673.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.58-9029_58-9026del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | ||||||
chr17:4869245 | ATTATTTA others(1): Show |
A | 14 | a0001c0001t0009g0215 a0001c0001t0009g0216 a0001c0001t0009g0217 others(11): Show |
14 | HG01168.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.58-9033_58-9026del others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | ||||||
chr17:4869245 | ATTATTTA others(5): Show |
A | 7 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(4): Show |
7 | HG02055.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-9037_58-9026del others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | ||||||
chr17:4869245 | ATTATTTA others(13): Show |
A | 135 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.58-9045_58-9026del others(20): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869245 | ||||||
chr17:4869333 | A | G | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58-8984A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869333 | |||||||
chr17:4869345 | C | T | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-8972C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869345 | |||||||
chr17:4869397 | C | A | 1 | a0001c0001t0002g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.58-8920C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869397 | |||||||
chr17:4869405 | T | C | 1 | a0001c0001t0018g0314 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-8912T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869405 | |||||||
chr17:4869466 | G | A | 54 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(51): Show |
54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-8851G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869466 | |||||||
chr17:4869467 | G | A | 54 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(51): Show |
54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-8850G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869467 | |||||||
chr17:4869502 | C | T | 1 | a0001c0005t0008g0229 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.58-8815C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869502 | |||||||
chr17:4869513 | GTGATCCT others(251): Show |
G | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58-8803_58-8546del | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869513 | |||||||
chr17:4869626 | C | T | 1 | a0001c0004t0006g0136 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.58-8691C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869626 | |||||||
chr17:4869749 | C | CT | 9 | a0001c0001t0009g0279 a0001c0004t0019g0333 a0001c0004t0019g0343 others(6): Show |
9 | HG00140.hp1 HG01109.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-8557dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869749 | ||||||
chr17:4869749 | C | CTT | 20 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(17): Show |
20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.58-8558_58-8557dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869749 | ||||||
chr17:4869749 | C | T | 1 | a0001c0004t0006g0339 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.58-8568C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869749 | |||||||
chr17:4869749 | CT | C | 8 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(5): Show |
8 | HG00140.hp2 HG00673.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-8557delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869749 | ||||||
chr17:4869821 | G | GTTTA | 5 | a0001c0001t0007g0093 a0001c0001t0014g0092 a0001c0004t0006g0339 others(2): Show |
5 | NA18943.hp1 NA18973.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-8468_58-8465dup others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | ||||||
chr17:4869821 | G | GTTTATTT others(1): Show |
20 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(17): Show |
20 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.58-8472_58-8465dup others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | ||||||
chr17:4869821 | G | GTTTATTT others(5): Show |
2 | a0001c0004t0006g0344 a0001c0004t0006g0345 |
2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.58-8476_58-8465dup others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | ||||||
chr17:4869821 | GTTTA | G | 164 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.58-8468_58-8465del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869821 | ||||||
chr17:4869825 | A | G | 1 | a0003c0003t0011g0044 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.58-8492A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869825 | |||||||
chr17:4869837 | A | G | 1 | a0001c0001t0005g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58-8480A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869837 | |||||||
chr17:4869914 | C | CT | 11 | a0001c0005t0006g0233 a0001c0005t0008g0227 a0001c0005t0008g0228 others(8): Show |
11 | HG00642.hp2 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-8393dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4869914 | ||||||
chr17:4869991 | C | T | 1 | a0002c0002t0015g0296 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.58-8326C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4869991 | |||||||
chr17:4870134 | G | A | 36 | a0001c0001t0002g0137 a0001c0001t0009g0204 a0001c0001t0009g0205 others(33): Show |
36 | HG00642.hp2 HG00673.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.58-8183G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870134 | |||||||
chr17:4870207 | C | T | 1 | a0005c0009t0053g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-8110C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870207 | |||||||
chr17:4870213 | A | AT | 11 | a0001c0001t0002g0129 a0001c0001t0004g0248 a0001c0001t0004g0249 others(8): Show |
11 | HG01358.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-8083dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4870213 | ||||||
chr17:4870213 | AT | A | 28 | a0001c0001t0002g0184 a0001c0001t0002g0196 a0001c0001t0021g0079 others(25): Show |
28 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.58-8083delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4870213 | ||||||
chr17:4870213 | ATT | A | 30 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(27): Show |
30 | HG00642.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.58-8084_58-8083del others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4870213 | ||||||
chr17:4870277 | G | A | 1 | a0003c0003t0003g0035 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58-8040G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870277 | |||||||
chr17:4870296 | T | C | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58-8021T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870296 | |||||||
chr17:4870526 | C | T | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.58-7791C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870526 | |||||||
chr17:4870695 | C | T | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-7622C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870695 | |||||||
chr17:4870789 | C | T | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-7528C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870789 | |||||||
chr17:4870794 | C | T | 1 | a0001c0004t0027g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.58-7523C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4870794 | |||||||
chr17:4871046 | G | A | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-7271G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871046 | |||||||
chr17:4871181 | A | AT | 13 | a0001c0001t0002g0137 a0001c0001t0002g0164 a0001c0001t0002g0176 others(10): Show |
13 | HG01243.hp2 HG01261.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-7114dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4871181 | ||||||
chr17:4871181 | A | ATT | 20 | a0001c0001t0018g0314 a0001c0004t0006g0332 a0001c0004t0006g0336 others(17): Show |
20 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-7115_58-7114dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4871181 | ||||||
chr17:4871181 | AT | A | 86 | a0001c0001t0002g0184 a0001c0001t0002g0189 a0001c0001t0003g0063 others(83): Show |
87 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.58-7114delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4871181 | ||||||
chr17:4871373 | G | A | 1 | a0002c0002t0004g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.58-6944G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871373 | |||||||
chr17:4871465 | G | A | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-6852G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871465 | |||||||
chr17:4871492 | A | G | 4 | a0004c0006t0012g0090 a0004c0006t0012g0102 a0004c0006t0012g0114 others(1): Show |
4 | HG00621.hp2 NA18966.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-6825A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871492 | |||||||
chr17:4871519 | C | G | 1 | a0002c0002t0001g0299 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.58-6798C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871519 | |||||||
chr17:4871685 | T | C | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58-6632T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871685 | |||||||
chr17:4871947 | T | C | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-6370T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4871947 | |||||||
chr17:4872054 | G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-6263G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872054 | |||||||
chr17:4872140 | G | A | 1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-6177G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872140 | |||||||
chr17:4872329 | T | TA | 14 | a0001c0001t0002g0192 a0001c0001t0012g0096 a0001c0001t0024g0209 others(11): Show |
14 | HG01167.hp1 HG01517.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.58-5971dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4872329 | ||||||
chr17:4872330 | A | T | 1 | a0001c0001t0007g0117 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.58-5987A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872330 | |||||||
chr17:4872456 | G | C | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.58-5861G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872456 | |||||||
chr17:4872539 | G | A | 5 | a0001c0001t0020g0148 a0001c0001t0024g0209 a0001c0001t0024g0219 others(2): Show |
5 | HG01167.hp1 HG02486.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-5778G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872539 | |||||||
chr17:4872588 | T | G | 1 | a0001c0001t0009g0212 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-5729T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872588 | |||||||
chr17:4872838 | G | A | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-5479G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872838 | |||||||
chr17:4872986 | G | A | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.58-5331G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4872986 | |||||||
chr17:4873109 | C | A | 1 | a0003c0003t0039g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.58-5208C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873109 | |||||||
chr17:4873272 | C | CACAATAG others(73): Show |
1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-4824_58-4745dup others(80): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873272 | ||||||
chr17:4873272 | CACAATAG others(73): Show |
C | 1 | a0002c0002t0015g0276 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.58-4824_58-4745del others(80): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873272 | ||||||
chr17:4873317 | A | G | 2 | a0003c0003t0003g0010 a0003c0013t0003g0057 |
2 | NA18962.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.58-5000A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873317 | |||||||
chr17:4873395 | A | G | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4922A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873395 | |||||||
chr17:4873423 | G | A | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4894G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873423 | |||||||
chr17:4873433 | A | G | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4884A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873433 | |||||||
chr17:4873475 | A | G | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4842A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873475 | |||||||
chr17:4873584 | C | T | 138 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.58-4733C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873584 | |||||||
chr17:4873617 | C | CT | 81 | a0001c0001t0002g0177 a0001c0001t0002g0184 a0001c0001t0002g0189 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.58-4681dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | ||||||
chr17:4873617 | C | CTT | 49 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(46): Show |
50 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-4682_58-4681dup others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | ||||||
chr17:4873617 | C | CTTT | 6 | a0001c0001t0002g0163 a0001c0001t0004g0182 a0001c0001t0016g0223 others(3): Show |
6 | HG01361.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-4683_58-4681dup others(3): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | ||||||
chr17:4873617 | CT | C | 29 | a0001c0001t0005g0116 a0001c0001t0009g0204 a0001c0001t0009g0205 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4681delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4873617 | ||||||
chr17:4873637 | G | A | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4680G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873637 | |||||||
chr17:4873679 | C | T | 1 | a0001c0001t0008g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58-4638C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873679 | |||||||
chr17:4873912 | G | T | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-4405G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873912 | |||||||
chr17:4873974 | G | A | 2 | a0001c0004t0006g0341 a0001c0004t0027g0074 |
2 | NA18968.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.58-4343G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4873974 | |||||||
chr17:4874192 | GTGAGCTC others(35): Show |
G | 1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-4122_58-4081del others(42): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4874192 | ||||||
chr17:4874339 | T | C | 54 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(51): Show |
54 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.58-3978T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874339 | |||||||
chr17:4874378 | G | A | 5 | a0001c0005t0008g0227 a0001c0005t0008g0228 a0001c0005t0008g0229 others(2): Show |
5 | HG00642.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-3939G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874378 | |||||||
chr17:4874499 | A | G | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-3818A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874499 | |||||||
chr17:4874532 | G | C | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-3785G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874532 | |||||||
chr17:4874809 | A | G | 2 | a0001c0005t0006g0233 a0001c0005t0008g0232 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.58-3508A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874809 | |||||||
chr17:4874894 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-3423G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874894 | |||||||
chr17:4874981 | G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-3336G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4874981 | |||||||
chr17:4875002 | G | A | 1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-3315G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875002 | |||||||
chr17:4875020 | T | C | 1 | a0001c0005t0054g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58-3297T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875020 | |||||||
chr17:4875192 | G | A | 133 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.58-3125G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875192 | |||||||
chr17:4875323 | G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-2994G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875323 | |||||||
chr17:4875348 | G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58-2969G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875348 | |||||||
chr17:4875355 | A | G | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-2962A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875355 | |||||||
chr17:4875378 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.58-2939G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875378 | |||||||
chr17:4875713 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-2604G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875713 | |||||||
chr17:4875727 | G | T | 1 | a0001c0005t0008g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.58-2590G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875727 | |||||||
chr17:4875796 | G | GT | 9 | a0001c0001t0002g0137 a0001c0001t0025g0132 a0001c0001t0025g0138 others(6): Show |
9 | HG00673.hp2 NA18939.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-2513dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4875796 | ||||||
chr17:4875810 | C | T | 1 | a0001c0008t0002g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.58-2507C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875810 | |||||||
chr17:4875814 | G | A | 74 | a0001c0001t0002g0281 a0001c0001t0009g0279 a0001c0001t0018g0259 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.58-2503G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875814 | |||||||
chr17:4875835 | G | A | 3 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 |
3 | HG01167.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-2482G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875835 | |||||||
chr17:4875928 | T | C | 1 | a0002c0002t0004g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.58-2389T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4875928 | |||||||
chr17:4876016 | C | T | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58-2301C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876016 | |||||||
chr17:4876058 | G | A | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.58-2259G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876058 | |||||||
chr17:4876098 | A | ATTTTTTT others(29): Show |
1 | a0003c0003t0026g0082 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-2209_58-2208ins others(36): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4876098 | ||||||
chr17:4876202 | C | G | 29 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(26): Show |
29 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-2115C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876202 | |||||||
chr17:4876350 | G | GT | 23 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(20): Show |
23 | HG00642.hp2 HG01168.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.58-1967_58-1966ins others(1): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876350 | |||||||
chr17:4876435 | A | T | 1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-1882A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876435 | |||||||
chr17:4876436 | T | G | 1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-1881T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876436 | |||||||
chr17:4876438 | G | A | 1 | a0001c0001t0029g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-1879G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876438 | |||||||
chr17:4876580 | C | T | 51 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(48): Show |
55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.58-1737C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876580 | |||||||
chr17:4876770 | A | T | 17 | a0001c0001t0018g0314 a0001c0005t0002g0152 a0001c0005t0008g0227 others(14): Show |
17 | HG00642.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.58-1547A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876770 | |||||||
chr17:4876799 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58-1518G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4876799 | |||||||
chr17:4877332 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58-985T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877332 | |||||||
chr17:4877414 | G | A | 6 | a0001c0001t0002g0162 a0001c0001t0002g0170 a0001c0001t0002g0171 others(3): Show |
6 | NA18940.hp1 NA18950.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-903G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877414 | |||||||
chr17:4877500 | G | A | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.58-817G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877500 | |||||||
chr17:4877728 | A | T | 139 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.58-589A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877728 | |||||||
chr17:4877809 | C | CT | 36 | a0001c0001t0002g0173 a0001c0001t0002g0202 a0001c0001t0005g0211 others(33): Show |
36 | HG00621.hp2 HG00642.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.58-489dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4877809 | ||||||
chr17:4877809 | CT | C | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-489delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 4877809 | ||||||
chr17:4877896 | T | C | 2 | a0001c0001t0025g0132 a0001c0001t0025g0138 |
2 | NA18970.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.58-421T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4877896 | |||||||
chr17:4878012 | G | A | 1 | a0003c0003t0011g0019 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-305G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878012 | |||||||
chr17:4878046 | G | A | 1 | a0005c0009t0053g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-271G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878046 | |||||||
chr17:4878071 | A | G | 74 | a0001c0001t0009g0279 a0001c0001t0018g0259 a0001c0001t0018g0314 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.58-246A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878071 | |||||||
chr17:4878099 | C | T | 4 | a0001c0001t0016g0223 a0001c0001t0016g0224 a0001c0001t0016g0225 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-218C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878099 | |||||||
chr17:4878194 | C | T | 3 | a0001c0001t0005g0119 a0001c0001t0013g0075 a0001c0001t0031g0087 |
3 | NA18947.hp2 NA18948.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.58-123C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878194 | |||||||
chr17:4878255 | C | G | 1 | a0001c0005t0008g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58-62C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 1/31 | chr17 | 4878255 | |||||||
chr17:4878497 | A | G | 1 | a0001c0001t0013g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.123+115A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878497 | |||||||
chr17:4878595 | G | A | 138 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.123+213G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878595 | |||||||
chr17:4878672 | G | C | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123+290G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878672 | |||||||
chr17:4878941 | G | T | 1 | a0003c0003t0038g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.123+559G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4878941 | |||||||
chr17:4878998 | AAGGTGGC others(162): Show |
A | 1 | a0003c0003t0003g0037 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.123+636_123+804del | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4878998 | ||||||
chr17:4879018 | C | CACACTTG others(330): Show |
1 | a0001c0001t0005g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123+871_123+872ins others(337): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4879018 | ||||||
chr17:4879032 | GGGAGCCG others(106): Show |
G | 3 | a0003c0003t0003g0011 a0003c0003t0003g0027 a0003c0003t0003g0073 |
3 | HG02155.hp2 NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.123+692_123+804del | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4879032 | ||||||
chr17:4879200 | T | TGGGAGCC others(49): Show |
43 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(40): Show |
43 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.123+860_123+861ins others(56): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4879200 | ||||||
chr17:4879264 | G | A | 1 | a0001c0001t0025g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.123+882G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879264 | |||||||
chr17:4879629 | C | T | 71 | a0001c0001t0003g0063 a0001c0004t0027g0060 a0003c0003t0003g0006 others(68): Show |
72 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.123+1247C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879629 | |||||||
chr17:4879642 | C | G | 51 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(48): Show |
55 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.123+1260C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879642 | |||||||
chr17:4879702 | G | A | 138 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.124-1282G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879702 | |||||||
chr17:4879764 | G | A | 1 | a0003c0003t0011g0028 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.124-1220G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4879764 | |||||||
chr17:4880043 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.124-941G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880043 | |||||||
chr17:4880045 | C | G | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.124-939C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880045 | |||||||
chr17:4880280 | G | A | 1 | a0001c0001t0032g0194 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124-704G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880280 | |||||||
chr17:4880300 | C | CT | 20 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(17): Show |
20 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-669dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4880300 | ||||||
chr17:4880349 | G | A | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-635G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880349 | |||||||
chr17:4880540 | G | A | 1 | a0001c0004t0016g0352 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124-444G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880540 | |||||||
chr17:4880582 | C | T | 1 | a0001c0001t0025g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.124-402C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880582 | |||||||
chr17:4880628 | G | A | 1 | a0001c0018t0004g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-356G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880628 | |||||||
chr17:4880720 | A | G | 1 | a0010c0026t0003g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.124-264A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880720 | |||||||
chr17:4880757 | G | A | 1 | a0005c0009t0053g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.124-227G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880757 | |||||||
chr17:4880789 | A | G | 11 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-195A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880789 | |||||||
chr17:4880882 | A | C | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.124-102A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880882 | |||||||
chr17:4880886 | C | T | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-98C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880886 | |||||||
chr17:4880899 | C | CA | 12 | a0001c0004t0006g0136 a0002c0002t0001g0256 a0002c0002t0001g0270 others(9): Show |
12 | HG00733.hp1 HG01256.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-75dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 4880899 | ||||||
chr17:4880954 | A | C | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.124-30A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 2/31 | chr17 | 4880954 | |||||||
chr17:4881078 | G | T | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.180+38G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 3/31 | chr17 | 4881078 | |||||||
chr17:4881279 | G | A | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.306+22G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881279 | |||||||
chr17:4881431 | G | A | 44 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(41): Show |
45 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.306+174G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881431 | |||||||
chr17:4881538 | G | A | 1 | a0002c0002t0001g0111 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.306+281G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881538 | |||||||
chr17:4881548 | TAATA | T | 6 | a0002c0002t0002g0309 a0002c0002t0014g0289 a0002c0002t0014g0290 others(3): Show |
6 | NA18950.hp1 NA18969.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+300_306+303del others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4881548 | ||||||
chr17:4881664 | A | C | 1 | a0002c0002t0001g0321 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.306+407A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881664 | |||||||
chr17:4881684 | C | T | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.306+427C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881684 | |||||||
chr17:4881993 | T | C | 1 | a0002c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.306+736T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4881993 | |||||||
chr17:4882136 | C | G | 1 | a0001c0001t0002g0200 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.306+879C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882136 | |||||||
chr17:4882285 | A | G | 1 | a0001c0001t0004g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.306+1028A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882285 | |||||||
chr17:4882523 | A | G | 2 | a0002c0002t0001g0262 a0002c0002t0001g0263 |
2 | HG01106.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.306+1266A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882523 | |||||||
chr17:4882530 | T | C | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.306+1273T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882530 | |||||||
chr17:4882540 | A | C | 2 | a0001c0005t0006g0233 a0001c0005t0008g0232 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.306+1283A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882540 | |||||||
chr17:4882552 | T | A | 187 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.306+1295T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882552 | |||||||
chr17:4882664 | G | A | 43 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(40): Show |
43 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.306+1407G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882664 | |||||||
chr17:4882746 | G | C | 1 | a0003c0003t0026g0013 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.306+1489G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882746 | |||||||
chr17:4882879 | G | A | 10 | a0002c0002t0001g0005 a0002c0002t0001g0315 a0002c0002t0001g0316 others(7): Show |
11 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1484G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882879 | |||||||
chr17:4882950 | G | A | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.307-1413G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4882950 | |||||||
chr17:4883061 | C | T | 1 | a0001c0004t0027g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.307-1302C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883061 | |||||||
chr17:4883120 | C | CA | 8 | a0001c0001t0024g0219 a0001c0004t0016g0352 a0002c0002t0014g0308 others(5): Show |
8 | HG03098.hp2 NA18950.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1228dupA | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883120 | ||||||
chr17:4883209 | C | CT | 31 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(28): Show |
31 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.307-1141dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883209 | ||||||
chr17:4883209 | CT | C | 9 | a0001c0001t0002g0200 a0001c0001t0004g0248 a0001c0001t0004g0249 others(6): Show |
9 | HG01175.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1141delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883209 | ||||||
chr17:4883315 | C | G | 1 | a0001c0001t0021g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.307-1048C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883315 | |||||||
chr17:4883329 | T | C | 1 | a0001c0001t0004g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.307-1034T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883329 | |||||||
chr17:4883358 | C | T | 1 | a0001c0005t0008g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.307-1005C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883358 | |||||||
chr17:4883394 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.307-969T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883394 | |||||||
chr17:4883411 | A | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0222 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.307-952A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883411 | |||||||
chr17:4883418 | A | C | 1 | a0002c0002t0001g0320 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.307-945A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883418 | |||||||
chr17:4883428 | A | T | 1 | a0001c0001t0029g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-935A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883428 | |||||||
chr17:4883429 | T | C | 1 | a0001c0001t0029g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-934T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883429 | |||||||
chr17:4883443 | A | G | 23 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.307-920A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883443 | |||||||
chr17:4883451 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.307-912G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883451 | |||||||
chr17:4883472 | A | G | 48 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(45): Show |
52 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.307-891A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883472 | |||||||
chr17:4883486 | G | A | 1 | a0001c0001t0007g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.307-877G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883486 | |||||||
chr17:4883625 | G | A | 1 | a0001c0018t0004g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307-738G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883625 | |||||||
chr17:4883636 | G | A | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.307-727G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883636 | |||||||
chr17:4883688 | C | T | 1 | a0002c0002t0001g0304 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.307-675C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883688 | |||||||
chr17:4883698 | C | CT | 23 | a0001c0001t0002g0171 a0001c0001t0002g0191 a0001c0001t0004g0182 others(20): Show |
23 | HG00642.hp1 HG00738.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.307-644dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883698 | ||||||
chr17:4883698 | CT | C | 47 | a0001c0001t0007g0109 a0001c0004t0006g0329 a0001c0004t0006g0332 others(44): Show |
47 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.307-644delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4883698 | ||||||
chr17:4883720 | A | G | 1 | a0003c0007t0003g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.307-643A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883720 | |||||||
chr17:4883738 | C | A | 1 | a0002c0002t0001g0270 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.307-625C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883738 | |||||||
chr17:4883789 | C | T | 6 | a0002c0002t0004g0140 a0002c0002t0004g0142 a0002c0002t0004g0144 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-574C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883789 | |||||||
chr17:4883827 | C | T | 1 | a0002c0002t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.307-536C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883827 | |||||||
chr17:4883858 | C | T | 1 | a0001c0001t0005g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.307-505C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883858 | |||||||
chr17:4883966 | G | A | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.307-397G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883966 | |||||||
chr17:4883977 | C | G | 18 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(15): Show |
18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-386C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4883977 | |||||||
chr17:4884028 | C | CT | 14 | a0001c0001t0002g0171 a0001c0001t0004g0182 a0001c0001t0009g0204 others(11): Show |
14 | HG01168.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.307-317dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4884028 | ||||||
chr17:4884028 | CT | C | 46 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(43): Show |
46 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.307-317delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 4884028 | ||||||
chr17:4884051 | C | T | 5 | a0002c0002t0001g0304 a0002c0002t0001g0310 a0002c0002t0001g0327 others(2): Show |
5 | HG00423.hp2 NA18988.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-312C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884051 | |||||||
chr17:4884077 | G | A | 141 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(138): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.307-286G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884077 | |||||||
chr17:4884103 | G | T | 2 | a0002c0002t0001g0316 a0002c0002t0001g0323 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.307-260G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884103 | |||||||
chr17:4884131 | T | C | 18 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(15): Show |
18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-232T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884131 | |||||||
chr17:4884174 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.307-189C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884174 | |||||||
chr17:4884230 | G | T | 1 | a0002c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.307-133G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 4/31 | chr17 | 4884230 | |||||||
chr17:4884486 | C | A | 1 | a0002c0002t0001g0254 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.417+13C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/31 | chr17 | 4884486 | |||||||
chr17:4884509 | G | A | 24 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(21): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.417+36G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/31 | chr17 | 4884509 | |||||||
chr17:4884519 | C | T | 1 | a0002c0002t0001g0321 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.417+46C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 5/31 | chr17 | 4884519 | |||||||
chr17:4885028 | C | T | 1 | a0002c0002t0015g0296 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.508+26C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 6/31 | chr17 | 4885028 | |||||||
chr17:4885320 | C | T | 1 | a0003c0003t0003g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.509-163C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 6/31 | chr17 | 4885320 | |||||||
chr17:4885589 | C | CCCTGATG others(117): Show |
1 | a0010c0026t0003g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.639+36_639+37insGA others(122): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr17 | 4885589 | ||||||
chr17:4885676 | G | A | 7 | a0001c0001t0004g0248 a0001c0001t0004g0249 a0001c0001t0004g0250 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+63G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 7/31 | chr17 | 4885676 | |||||||
chr17:4886117 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.695-3C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 8/31 | chr17 | 4886117 | |||||||
chr17:4886406 | C | G | 16 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(13): Show |
16 | HG00673.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-45C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 9/31 | chr17 | 4886406 | |||||||
chr17:4886666 | C | T | 25 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(22): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.949+40C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886666 | |||||||
chr17:4886933 | C | G | 1 | a0003c0003t0010g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.950-177C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886933 | |||||||
chr17:4886936 | T | TC | 43 | a0001c0004t0006g0329 a0001c0004t0006g0332 a0001c0004t0006g0336 others(40): Show |
43 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.950-172dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr17 | 4886936 | ||||||
chr17:4886961 | C | T | 7 | a0002c0002t0004g0257 a0002c0002t0004g0266 a0002c0002t0004g0267 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.950-149C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886961 | |||||||
chr17:4886962 | C | T | 1 | a0002c0002t0001g0298 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.950-148C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 10/31 | chr17 | 4886962 | |||||||
chr17:4887506 | G | GC | 73 | a0001c0001t0002g0187 a0001c0001t0002g0222 a0001c0001t0003g0063 others(70): Show |
74 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1020-73dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr17 | 4887506 | ||||||
chr17:4887822 | G | A | 1 | a0003c0003t0003g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1230+32G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4887822 | |||||||
chr17:4887823 | C | T | 18 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(15): Show |
18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1230+33C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4887823 | |||||||
chr17:4888061 | C | T | 77 | a0001c0001t0002g0187 a0001c0001t0002g0222 a0001c0001t0003g0063 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1230+271C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888061 | |||||||
chr17:4888110 | G | A | 1 | a0002c0002t0001g0280 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1230+320G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888110 | |||||||
chr17:4888124 | G | T | 1 | a0001c0001t0007g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1230+334G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888124 | |||||||
chr17:4888237 | C | T | 1 | a0001c0017t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1230+447C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888237 | |||||||
chr17:4888270 | A | C | 1 | a0005c0023t0009g0353 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1230+480A>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888270 | |||||||
chr17:4888400 | G | A | 73 | a0001c0001t0009g0279 a0001c0001t0056g0258 a0002c0002t0001g0005 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1230+610G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888400 | |||||||
chr17:4888413 | G | A | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230+623G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888413 | |||||||
chr17:4888440 | A | G | 1 | a0001c0001t0051g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1230+650A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888440 | |||||||
chr17:4888664 | C | T | 1 | a0003c0003t0003g0051 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1230+874C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888664 | |||||||
chr17:4888690 | C | CT | 45 | a0001c0001t0004g0182 a0001c0004t0006g0329 a0001c0004t0006g0332 others(42): Show |
45 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1230+920dupT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | ||||||
chr17:4888690 | CT | C | 185 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0154 others(182): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1230+920delT | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | ||||||
chr17:4888690 | CTT | C | 16 | a0001c0001t0002g0183 a0001c0001t0004g0248 a0001c0001t0004g0249 others(13): Show |
16 | HG01993.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1230+919_1230+920d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | ||||||
chr17:4888690 | CTTT | C | 13 | a0001c0005t0006g0233 a0001c0005t0008g0227 a0001c0005t0008g0228 others(10): Show |
13 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1230+918_1230+920d others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr17 | 4888690 | ||||||
chr17:4888710 | T | C | 18 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(15): Show |
18 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1230+920T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888710 | |||||||
chr17:4888772 | C | T | 5 | a0001c0001t0046g0198 a0001c0001t0055g0199 a0001c0008t0002g0156 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-875C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888772 | |||||||
chr17:4888774 | C | A | 132 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1231-873C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888774 | |||||||
chr17:4888786 | C | T | 1 | a0002c0002t0001g0264 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1231-861C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888786 | |||||||
chr17:4888927 | C | T | 1 | a0003c0003t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1231-720C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888927 | |||||||
chr17:4888972 | T | C | 22 | a0001c0001t0002g0137 a0001c0001t0009g0204 a0001c0001t0009g0205 others(19): Show |
22 | HG00673.hp2 HG01167.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1231-675T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4888972 | |||||||
chr17:4889074 | C | A | 1 | a0003c0003t0003g0035 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1231-573C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889074 | |||||||
chr17:4889112 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1231-535T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889112 | |||||||
chr17:4889115 | G | T | 1 | a0003c0003t0011g0028 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1231-532G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889115 | |||||||
chr17:4889239 | G | A | 1 | a0001c0001t0046g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1231-408G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889239 | |||||||
chr17:4889283 | G | A | 2 | a0003c0003t0003g0033 a0003c0003t0003g0048 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1231-364G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889283 | |||||||
chr17:4889337 | C | T | 1 | a0001c0001t0005g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1231-310C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889337 | |||||||
chr17:4889376 | T | C | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1231-271T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889376 | |||||||
chr17:4889524 | G | A | 4 | a0001c0001t0024g0209 a0001c0001t0024g0219 a0005c0009t0053g0208 others(1): Show |
4 | HG01167.hp1 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-123G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889524 | |||||||
chr17:4889546 | C | G | 4 | a0001c0001t0016g0223 a0001c0001t0016g0224 a0001c0001t0016g0225 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-101C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889546 | |||||||
chr17:4889590 | G | A | 18 | a0001c0001t0004g0249 a0001c0005t0002g0152 a0001c0005t0006g0233 others(15): Show |
18 | HG00642.hp2 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-57G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889590 | |||||||
chr17:4889611 | G | A | 5 | a0001c0001t0025g0132 a0001c0001t0025g0138 a0001c0001t0025g0139 others(2): Show |
5 | HG00673.hp2 NA18970.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-36G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 12/31 | chr17 | 4889611 | |||||||
chr17:4889803 | C | T | 4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+40C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4889803 | |||||||
chr17:4889964 | C | T | 1 | a0001c0001t0055g0199 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1347+201C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4889964 | |||||||
chr17:4890072 | T | C | 76 | a0001c0001t0002g0187 a0001c0001t0002g0222 a0001c0001t0003g0063 others(73): Show |
77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1347+309T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4890072 | |||||||
chr17:4890354 | T | G | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1348-163T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 13/31 | chr17 | 4890354 | |||||||
chr17:4890848 | A | G | 3 | a0002c0002t0001g0256 a0002c0002t0001g0270 a0002c0002t0015g0271 |
3 | HG01257.hp2 HG01952.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1567-103A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 14/31 | chr17 | 4890848 | |||||||
chr17:4891195 | C | CGT | 3 | a0002c0002t0001g0254 a0002c0002t0001g0265 a0002c0002t0001g0306 |
3 | HG01167.hp2 HG03669.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1740+72_1740+73ins others(2): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891195 | ||||||
chr17:4891196 | G | A | 1 | a0003c0003t0003g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1740+72G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891196 | |||||||
chr17:4891197 | C | T | 130 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1740+73C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891197 | |||||||
chr17:4891198 | G | A | 91 | a0001c0001t0002g0187 a0001c0001t0002g0222 a0001c0001t0003g0063 others(88): Show |
92 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1740+74G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891198 | |||||||
chr17:4891198 | G | GCACGCAC others(5): Show |
1 | a0003c0003t0003g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1740+75_1740+76ins others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891198 | ||||||
chr17:4891200 | G | A | 5 | a0002c0002t0001g0254 a0002c0002t0001g0265 a0002c0002t0001g0306 others(2): Show |
5 | HG01167.hp2 HG02258.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+76G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891200 | |||||||
chr17:4891200 | G | GCA | 3 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 |
3 | HG02486.hp2 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1740+100_1740+101d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCACA | 66 | a0001c0001t0002g0129 a0001c0001t0002g0137 a0001c0001t0005g0001 others(63): Show |
70 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1740+98_1740+101du others(5): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCACACA | 6 | a0001c0001t0005g0119 a0001c0001t0007g0126 a0001c0001t0025g0139 others(3): Show |
6 | HG00673.hp2 HG02155.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1740+96_1740+101du others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCACACAC others(1): Show |
4 | a0001c0001t0023g0244 a0001c0001t0023g0245 a0001c0001t0023g0247 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1740+94_1740+101du others(9): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCACACAC others(3): Show |
63 | a0001c0001t0002g0187 a0001c0001t0002g0222 a0001c0001t0003g0063 others(60): Show |
64 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1740+92_1740+101du others(11): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCACACAC others(5): Show |
3 | a0001c0018t0004g0334 a0003c0003t0013g0058 a0010c0026t0003g0076 |
3 | HG01243.hp2 NA18994.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1740+90_1740+101du others(13): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCGCACAC others(1): Show |
3 | a0001c0005t0002g0152 a0001c0005t0022g0221 a0006c0025t0005g0147 |
3 | HG02965.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCGCACAC others(3): Show |
32 | a0001c0004t0006g0135 a0001c0004t0006g0136 a0001c0004t0006g0329 others(29): Show |
32 | HG00609.hp1 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCGCACAC others(5): Show |
4 | a0001c0004t0042g0346 a0001c0005t0008g0228 a0001c0005t0008g0229 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCGCACAC others(7): Show |
2 | a0001c0005t0008g0227 a0001c0005t0037g0059 |
2 | HG00642.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCGCGCAC others(3): Show |
3 | a0001c0004t0006g0339 a0001c0004t0006g0348 a0003c0003t0003g0064 |
3 | HG00621.hp1 NA19057.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1740+77_1740+78ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GCGCGCAC others(5): Show |
1 | a0003c0003t0003g0049 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1740+77_1740+78ins others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | G | GTACACAC others(3): Show |
1 | a0003c0003t0003g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1740+76_1740+77ins others(10): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891200 | |||||||
chr17:4891200 | GCA | G | 3 | a0001c0001t0021g0079 a0001c0001t0021g0080 a0001c0001t0021g0081 |
3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1740+100_1740+101d others(4): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891200 | GCACACA | G | 48 | a0001c0004t0019g0349 a0002c0002t0001g0005 a0002c0002t0001g0280 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1740+96_1740+101de others(7): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr17 | 4891200 | ||||||
chr17:4891202 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1740+78A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891202 | |||||||
chr17:4891206 | A | G | 2 | a0001c0005t0012g0150 a0001c0005t0022g0149 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1740+82A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891206 | |||||||
chr17:4891208 | A | G | 2 | a0002c0002t0001g0287 a0002c0002t0001g0302 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1740+84A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891208 | |||||||
chr17:4891235 | C | T | 2 | a0001c0011t0006g0335 a0001c0011t0041g0347 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1740+111C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891235 | |||||||
chr17:4891361 | G | A | 1 | a0001c0001t0023g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1741-95G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891361 | |||||||
chr17:4891426 | C | T | 1 | a0001c0001t0016g0226 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1741-30C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 15/31 | chr17 | 4891426 | |||||||
chr17:4891822 | C | T | 1 | a0001c0004t0006g0340 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2001+106C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891822 | |||||||
chr17:4891894 | C | T | 2 | a0001c0001t0004g0248 a0001c0001t0004g0249 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2001+178C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891894 | |||||||
chr17:4891911 | G | A | 2 | a0002c0002t0001g0307 a0002c0002t0001g0311 |
2 | NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2001+195G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891911 | |||||||
chr17:4891926 | C | T | 1 | a0001c0001t0051g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2001+210C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4891926 | |||||||
chr17:4892012 | C | T | 124 | a0001c0001t0002g0154 a0001c0001t0002g0161 a0001c0001t0002g0162 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.2002-137C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892012 | |||||||
chr17:4892094 | T | C | 1 | a0002c0002t0015g0296 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2002-55T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892094 | |||||||
chr17:4892102 | G | A | 1 | a0002c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2002-47G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892102 | |||||||
chr17:4892123 | C | T | 1 | a0001c0001t0005g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2002-26C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 16/31 | chr17 | 4892123 | |||||||
chr17:4892324 | TG | T | 156 | a0001c0001t0002g0154 a0001c0001t0002g0161 a0001c0001t0002g0163 others(153): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2088-73delG | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 4892324 | ||||||
chr17:4892325 | G | A | 107 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0162 others(104): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2088-77G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | chr17 | 4892325 | |||||||
chr17:4892329 | G | T | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2088-73G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | chr17 | 4892329 | |||||||
chr17:4892330 | T | G | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2088-72T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | chr17 | 4892330 | |||||||
chr17:4892359 | G | GC | 11 | a0001c0001t0002g0137 a0001c0001t0002g0177 a0001c0011t0041g0347 others(8): Show |
11 | HG01952.hp1 HG01981.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2088-36dupC | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 4892359 | ||||||
chr17:4892907 | G | C | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2312-72G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/31 | chr17 | 4892907 | |||||||
chr17:4892908 | G | T | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2312-71G>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/31 | chr17 | 4892908 | |||||||
chr17:4892976 | C | T | 47 | a0001c0001t0002g0129 a0001c0001t0005g0001 a0001c0001t0005g0088 others(44): Show |
51 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(48): Show |
splice_region_variant&intron_variant | LOW | c.2312-3C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 19/31 | chr17 | 4892976 | |||||||
chr17:4893139 | A | G | 1 | a0001c0001t0021g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2400+72A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893139 | |||||||
chr17:4893146 | G | C | 74 | a0001c0001t0003g0063 a0001c0001t0007g0117 a0001c0001t0023g0244 others(71): Show |
75 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2400+79G>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893146 | |||||||
chr17:4893165 | G | A | 1 | a0001c0001t0007g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2400+98G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893165 | |||||||
chr17:4893203 | T | A | 1 | a0001c0005t0054g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2400+136T>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893203 | |||||||
chr17:4893215 | TTCCTAAC others(5): Show |
T | 23 | a0001c0001t0005g0166 a0001c0001t0020g0148 a0001c0004t0019g0349 others(20): Show |
23 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.2400+174_2401-182d others(14): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr17 | 4893215 | ||||||
chr17:4893226 | T | G | 90 | a0001c0001t0002g0137 a0001c0001t0003g0063 a0001c0001t0007g0117 others(87): Show |
91 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2400+159T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893226 | |||||||
chr17:4893251 | C | T | 5 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(2): Show |
5 | HG01358.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401-183C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893251 | |||||||
chr17:4893361 | T | C | 116 | a0001c0001t0002g0004 a0001c0001t0002g0137 a0001c0001t0002g0154 others(113): Show |
117 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.2401-73T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893361 | |||||||
chr17:4893365 | C | T | 7 | a0001c0001t0007g0086 a0001c0001t0007g0101 a0001c0001t0007g0104 others(4): Show |
7 | HG00280.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2401-69C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 20/31 | chr17 | 4893365 | |||||||
chr17:4893618 | C | A | 1 | a0001c0001t0052g0134 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2564+21C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893618 | |||||||
chr17:4893620 | C | T | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2564+23C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893620 | |||||||
chr17:4893621 | T | C | 1 | a0007c0022t0004g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2564+24T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893621 | |||||||
chr17:4893776 | C | A | 18 | a0001c0005t0002g0152 a0001c0005t0006g0233 a0001c0005t0008g0227 others(15): Show |
18 | HG00642.hp2 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2564+179C>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 21/31 | chr17 | 4893776 | |||||||
chr17:4894137 | C | T | 12 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(9): Show |
12 | HG01109.hp1 HG01168.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2671-37C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 22/31 | chr17 | 4894137 | |||||||
chr17:4894322 | C | T | 1 | a0001c0004t0006g0338 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2808+11C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894322 | |||||||
chr17:4894323 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2808+12G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894323 | |||||||
chr17:4894338 | G | A | 2 | a0001c0001t0024g0209 a0001c0001t0024g0219 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2808+27G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894338 | |||||||
chr17:4894423 | C | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(76): Show |
80 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.2809-102C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 23/31 | chr17 | 4894423 | |||||||
chr17:4894639 | G | A | 1 | a0001c0004t0006g0348 | 1 | HG00621.hp1 | splice_region_variant&intron_variant | LOW | c.2917+6G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/31 | chr17 | 4894639 | |||||||
chr17:4894673 | C | T | 9 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2917+40C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/31 | chr17 | 4894673 | |||||||
chr17:4894956 | G | A | 1 | a0002c0002t0004g0257 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2918-119G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 24/31 | chr17 | 4894956 | |||||||
chr17:4895279 | G | A | 1 | a0003c0003t0026g0013 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3085+37G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 25/31 | chr17 | 4895279 | |||||||
chr17:4895567 | G | A | 17 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(14): Show |
17 | HG00673.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.3229+74G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/31 | chr17 | 4895567 | |||||||
chr17:4895607 | C | G | 1 | a0006c0021t0007g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3230-91C>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/31 | chr17 | 4895607 | |||||||
chr17:4895647 | C | T | 1 | a0001c0001t0009g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3230-51C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 26/31 | chr17 | 4895647 | |||||||
chr17:4895941 | C | T | 54 | a0001c0001t0002g0004 a0001c0001t0002g0154 a0001c0001t0002g0155 others(51): Show |
55 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.3365-62C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 27/31 | chr17 | 4895941 | |||||||
chr17:4896353 | C | T | 1 | a0001c0001t0020g0148 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3615+11C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 29/31 | chr17 | 4896353 | |||||||
chr17:4896398 | C | T | 1 | a0002c0002t0001g0324 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3616-31C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 29/31 | chr17 | 4896398 | |||||||
chr17:4896602 | C | T | 69 | a0001c0001t0003g0063 a0002c0002t0020g0288 a0002c0002t0020g0301 others(66): Show |
70 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.3775+14C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 30/31 | chr17 | 4896602 | |||||||
chr17:4896871 | CCTGGGCA others(5): Show |
C | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3915+64_3915+75del others(12): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 4896871 | ||||||
chr17:4896885 | T | G | 1 | a0001c0004t0019g0349 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3915+72T>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896885 | |||||||
chr17:4896885 | T | TG | 33 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(30): Show |
33 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.3915+76dupG | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 4896885 | ||||||
chr17:4896903 | G | A | 1 | a0006c0025t0005g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3915+90G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896903 | |||||||
chr17:4896938 | A | G | 319 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(316): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3915+125A>G | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896938 | |||||||
chr17:4896942 | G | A | 1 | a0001c0018t0004g0334 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3915+129G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896942 | |||||||
chr17:4896995 | C | T | 207 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(204): Show |
213 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.3915+182C>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4896995 | |||||||
chr17:4897009 | G | A | 169 | a0001c0001t0002g0004 a0001c0001t0002g0129 a0001c0001t0002g0137 others(166): Show |
171 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.3916-195G>A | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4897009 | |||||||
chr17:4897064 | A | T | 2 | a0003c0003t0003g0009 a0003c0003t0033g0020 |
2 | HG02083.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3916-140A>T | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4897064 | |||||||
chr17:4897112 | T | C | 12 | a0001c0001t0009g0204 a0001c0001t0009g0205 a0001c0001t0009g0212 others(9): Show |
12 | HG01109.hp1 HG01168.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.3916-92T>C | MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | chr17 | 4897112 | |||||||
chr17:4897129 | CCCTTCTT others(1): Show |
C | 4 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0018g0314 others(1): Show |
4 | HG01175.hp2 HG03098.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.3916-72_3916-65del others(8): Show |
MINK1 | ENSG00000141503.17 | transcript | ENST00000355280.11 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 4897129 |