Item | Value |
---|---|
geneid | 255231 |
ensemblid | ENSG00000153898.13 |
hgncid | 13357 |
symbol | MCOLN2 |
name | mucolipin TRP cation channel 2 |
refseq_nuc | NM_153259.4 |
refseq_prot | NP_694991.2 |
ensembl_nuc | ENST00000370608.8 |
ensembl_prot | ENSP00000359640.3 |
mane_status | MANE Select |
chr | chr1 |
start | 84925583 |
end | 84997113 |
strand | - |
ver | v1.2 |
region | chr1:84925583-84997113 |
region5000 | chr1:84920583-85002113 |
regionname0 | MCOLN2_chr1_84925583_84997113 |
regionname5000 | MCOLN2_chr1_84920583_85002113 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 566 | 316 | 56 | 63 | 150 | 12 | 33 | 112 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0002 | 0/0 | 566 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0003 | 0/0 | 566 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0004 | 0/0 | 566 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0005 | 0/0 | 566 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0006 | 0/0 | 566 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0007 | 0/0 | 566 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0008 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0009 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0010 | 0/0 | 566 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
a0011 | 0/0 | 566 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | MARQP others(561): Show |
chr1 | 84920583 | 85002113 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1698 | 315 | 56 | 63 | 149 | 12 | 33 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0001c0011 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0002c0002 | 0/0 | 1698 | 10 | 8 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0003c0003 | 0/0 | 1698 | 9 | 9 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0004c0004 | 0/0 | 1698 | 4 | 4 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0005c0006 | 0/0 | 1698 | 3 | 1 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0006c0005 | 0/0 | 1698 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0007c0010 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0008c0012 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0009c0007 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0010c0009 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 | ||
a0011c0008 | 0/0 | 1698 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ATGGC others(1693): Show |
chr1 | 84920583 | 85002113 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3044 | 72 | 22 | 12 | 28 | 3 | 7 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0002 | 0/0 | 3044 | 67 | 10 | 14 | 31 | 4 | 8 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0003 | 0/0 | 3044 | 50 | 0 | 19 | 23 | 2 | 6 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0004 | 0/0 | 3044 | 23 | 3 | 6 | 13 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0005 | 1/0 | 3044 | 12 | 11 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0006 | 0/0 | 3045 | 16 | 0 | 0 | 16 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0007 | 0/0 | 3045 | 14 | 0 | 1 | 8 | 0 | 5 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0008 | 0/0 | 3043 | 10 | 0 | 1 | 8 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3038): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0009 | 0/0 | 3043 | 9 | 0 | 2 | 7 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3038): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0010 | 0/0 | 3044 | 5 | 0 | 4 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0011 | 0/0 | 3043 | 4 | 0 | 0 | 1 | 0 | 3 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3038): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0012 | 0/0 | 3046 | 4 | 0 | 0 | 4 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3041): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0013 | 0/0 | 3044 | 2 | 1 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0014 | 0/0 | 3045 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0015 | 0/0 | 3046 | 3 | 0 | 1 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3041): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0016 | 0/0 | 3045 | 2 | 0 | 0 | 1 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0017 | 0/0 | 3044 | 2 | 0 | 1 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0018 | 0/0 | 3044 | 2 | 1 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0019 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0020 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0021 | 0/0 | 3044 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0022 | 0/0 | 3044 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0023 | 0/0 | 3043 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3038): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0025 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0026 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0028 | 0/0 | 3044 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0029 | 0/0 | 3044 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0030 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0031 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0032 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0033 | 0/0 | 3044 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0034 | 0/1 | 3046 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3041): Show |
chr1 | 84920583 | 85002113 |
a0001c0001t0035 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0001c0011t0004 | 0/0 | 3044 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0002c0002t0001 | 0/0 | 3044 | 5 | 5 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0002c0002t0002 | 0/0 | 3044 | 4 | 2 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0002c0002t0027 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3040): Show |
chr1 | 84920583 | 85002113 |
a0003c0003t0001 | 0/0 | 3044 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0003c0003t0005 | 0/0 | 3044 | 6 | 6 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0003c0003t0013 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0004c0004t0001 | 0/0 | 3044 | 4 | 4 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0005c0006t0001 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0005c0006t0003 | 0/0 | 3044 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0005c0006t0024 | 0/0 | 3044 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0006c0005t0001 | 0/0 | 3044 | 3 | 3 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0007c0010t0002 | 0/0 | 3044 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0008c0012t0005 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0009c0007t0004 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0010c0009t0001 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
a0011c0008t0002 | 0/0 | 3044 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | ACACA others(3039): Show |
chr1 | 84920583 | 85002113 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0006g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0010g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0010g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0010g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0010g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0010g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0011g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0011g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0011g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0012g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0012g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0012g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0012g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0015g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0015g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0016g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0016g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0017g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0017g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0018g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0018g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0019g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0020g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0021g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0022g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0023g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0025g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0026g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0028g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0029g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0030g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0031g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0032g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0033g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0034g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0001t0035g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0001c0011t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0002c0002t0027g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0003c0003t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0004c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0004c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0005c0006t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0005c0006t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0005c0006t0024g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0006c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0006c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0006c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0007c0010t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0008c0012t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0009c0007t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0010c0009t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
a0011c0008t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0240 | EUR | GBR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00140 | hp2 | a0001 | c0001 | t0016 | g0128 | EUR | GBR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00280 | hp1 | a0001 | c0001 | t0017 | g0103 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0274 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | FIN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00558 | hp1 | a0001 | c0001 | t0032 | g0278 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0171 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00642 | hp2 | a0007 | c0010 | t0002 | g0245 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00673 | hp2 | a0001 | c0001 | t0015 | g0176 | EAS | CHS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG00741 | hp2 | a0005 | c0006 | t0003 | g0325 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0129 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0333 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01099 | hp2 | a0005 | c0006 | t0024 | g0133 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0332 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0065 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0330 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01169 | hp1 | a0001 | c0001 | t0017 | g0159 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01257 | hp1 | a0001 | c0001 | t0029 | g0102 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0130 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01516 | hp1 | a0001 | c0001 | t0010 | g0329 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01884 | hp2 | a0003 | c0003 | t0005 | g0002 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0202 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01943 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01978 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0127 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG01993 | hp2 | a0001 | c0001 | t0020 | g0090 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0233 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02080 | hp1 | a0001 | c0001 | t0008 | g0211 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02080 | hp2 | a0001 | c0001 | t0008 | g0273 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02129 | hp1 | a0001 | c0011 | t0004 | g0114 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02145 | hp1 | a0008 | c0012 | t0005 | g0018 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02165 | hp1 | a0001 | c0001 | t0008 | g0216 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02257 | hp1 | a0004 | c0004 | t0001 | g0041 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02280 | hp2 | a0001 | c0001 | t0030 | g0089 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02300 | hp2 | a0001 | c0001 | t0010 | g0331 | AMR | PEL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02572 | hp1 | a0001 | c0001 | t0035 | g0319 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02572 | hp2 | a0009 | c0007 | t0004 | g0043 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02615 | hp2 | a0006 | c0005 | t0001 | g0047 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02622 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0087 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02647 | hp2 | a0001 | c0001 | t0025 | g0088 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0058 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0017 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02818 | hp2 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02896 | hp2 | a0003 | c0003 | t0005 | g0033 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02897 | hp1 | a0003 | c0003 | t0005 | g0030 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02922 | hp1 | a0006 | c0005 | t0001 | g0045 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02965 | hp2 | a0004 | c0004 | t0001 | g0046 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02976 | hp2 | a0003 | c0003 | t0005 | g0032 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03017 | hp2 | a0001 | c0001 | t0018 | g0225 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03098 | hp2 | a0010 | c0009 | t0001 | g0180 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03130 | hp1 | a0005 | c0006 | t0001 | g0132 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03130 | hp2 | a0001 | c0001 | t0031 | g0246 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0042 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0062 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03516 | hp1 | a0006 | c0005 | t0001 | g0044 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | MSL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03654 | hp1 | a0001 | c0001 | t0011 | g0223 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0166 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0288 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0028 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0085 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03927 | hp1 | a0011 | c0008 | t0002 | g0221 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03927 | hp2 | a0001 | c0001 | t0011 | g0269 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0053 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0076 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04228 | hp1 | a0001 | c0001 | t0008 | g0311 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG04228 | hp2 | a0001 | c0001 | t0011 | g0266 | SAS | STU | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18522 | hp2 | a0001 | c0001 | t0018 | g0244 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18612 | hp1 | a0001 | c0001 | t0015 | g0169 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18747 | hp1 | a0001 | c0001 | t0009 | g0051 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18941 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0098 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18948 | hp2 | a0001 | c0001 | t0026 | g0149 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18952 | hp1 | a0001 | c0001 | t0009 | g0109 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0110 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18954 | hp1 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18959 | hp1 | a0001 | c0001 | t0021 | g0165 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0297 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0308 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18968 | hp2 | a0001 | c0001 | t0028 | g0135 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18971 | hp1 | a0001 | c0001 | t0008 | g0227 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0300 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18973 | hp1 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18974 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18979 | hp1 | a0001 | c0001 | t0009 | g0052 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18983 | hp1 | a0001 | c0001 | t0012 | g0217 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18984 | hp2 | a0001 | c0001 | t0008 | g0272 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18986 | hp1 | a0001 | c0001 | t0023 | g0151 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18995 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0117 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19011 | hp1 | a0001 | c0001 | t0008 | g0219 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19012 | hp2 | a0001 | c0001 | t0012 | g0256 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0097 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19054 | hp2 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0302 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19058 | hp1 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19058 | hp2 | a0001 | c0001 | t0022 | g0144 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19062 | hp1 | a0001 | c0001 | t0006 | g0293 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19063 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19063 | hp2 | a0001 | c0001 | t0012 | g0259 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19067 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19074 | hp1 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19079 | hp2 | a0001 | c0001 | t0033 | g0315 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19080 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0154 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19085 | hp1 | a0001 | c0001 | t0016 | g0172 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19085 | hp2 | a0001 | c0001 | t0012 | g0261 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | ASW | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA20129 | hp2 | a0003 | c0003 | t0005 | g0002 | AFR | ASW | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | GIH | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | GIH | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02109 | hp2 | a0004 | c0004 | t0001 | g0048 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02486 | hp1 | a0002 | c0002 | t0027 | g0107 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG06807 | hp1 | a0003 | c0003 | t0013 | g0027 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0038 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA20300 | hp1 | a0001 | c0001 | t0013 | g0039 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | USA | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
homoSapiens | chm13v2 | a0001 | c0001 | t0034 | g0200 | REF | REF | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0024 | REF | REF | MCOLN2_chr1_84920583_85002113 | MCOLN2 | chr1 | 84920583 | 85002113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84931393 | G | A | 1 | a0009 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1511C>T | p.Ala504Val | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/14 | 1752/3044 | 1511/1701 | 504/566 | chr1 | 84931393 | |||
chr1:84939555 | T | G | 1 | a0003 | 9 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.1108A>C | p.Lys370Gln | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/14 | 1349/3044 | 1108/1701 | 370/566 | chr1 | 84939555 | |||
chr1:84939560 | T | A | 1 | a0005 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1103A>T | p.Lys368Ile | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/14 | 1344/3044 | 1103/1701 | 368/566 | chr1 | 84939560 | |||
chr1:84939570 | T | C | 2 | a0002 a0006 |
13 | HG00639.hp2 HG01167.hp2 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.1093A>G | p.Met365Val | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/14 | 1334/3044 | 1093/1701 | 365/566 | chr1 | 84939570 | |||
chr1:84940884 | G | A | 1 | a0005 | 3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.955C>T | p.Arg319Trp | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/14 | 1196/3044 | 955/1701 | 319/566 | chr1 | 84940884 | |||
chr1:84940979 | G | C | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.860C>G | p.Ala287Gly | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/14 | 1101/3044 | 860/1701 | 287/566 | chr1 | 84940979 | |||
chr1:84947033 | T | A | 1 | a0007 | 1 | HG00642.hp2 | missense_variant&splice_region_variant | MODERATE | c.847A>T | p.Thr283Ser | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/14 | 1088/3044 | 847/1701 | 283/566 | chr1 | 84947033 | |||
chr1:84965616 | C | T | 1 | a0011 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.170G>A | p.Arg57Gln | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/14 | 411/3044 | 170/1701 | 57/566 | chr1 | 84965616 | |||
chr1:84965692 | G | A | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.94C>T | p.Arg32Cys | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/14 | 335/3044 | 94/1701 | 32/566 | chr1 | 84965692 | |||
chr1:84996815 | C | T | 3 | a0004 a0006 a0009 |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.58G>A | p.Val20Ile | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 299/3044 | 58/1701 | 20/566 | chr1 | 84996815 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84929587 | G | T | 1 | a0007c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.1635C>A | p.Ala545Ala | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/14 | 1876/3044 | 1635/1701 | 545/566 | chr1 | 84929587 | |||
chr1:84956561 | G | A | 1 | a0001c0011 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.435C>T | p.Thr145Thr | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/14 | 676/3044 | 435/1701 | 145/566 | chr1 | 84956561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84925714 | A | G | 2 | a0001c0001t0014 a0002c0002t0027 |
4 | HG02486.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*971T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 971 | chr1 | 84925714 | ||||||
chr1:84925746 | C | T | 1 | a0001c0001t0026 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 939 | chr1 | 84925746 | ||||||
chr1:84925807 | T | C | 1 | a0001c0001t0033 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 878 | chr1 | 84925807 | ||||||
chr1:84925881 | A | C | 3 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0028 |
8 | HG00673.hp2 HG01981.hp2 NA18612.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*804T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 804 | chr1 | 84925881 | ||||||
chr1:84925892 | A | AT | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0014 others(8): Show |
42 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*792dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 792 | chr1 | 84925892 | ||||||
chr1:84925892 | AT | A | 4 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0011 others(1): Show |
24 | HG01928.hp2 HG01943.hp1 HG01978.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*792delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 792 | chr1 | 84925892 | ||||||
chr1:84925899 | T | TTG | 2 | a0001c0001t0012 a0001c0001t0015 |
7 | HG00673.hp2 HG01981.hp2 NA18612.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786insCA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 785 | chr1 | 84925899 | ||||||
chr1:84926013 | C | T | 2 | a0001c0001t0031 a0001c0001t0035 |
2 | HG02572.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*672G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 672 | chr1 | 84926013 | ||||||
chr1:84926046 | C | T | 2 | a0001c0001t0022 a0001c0001t0029 |
2 | HG01257.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*639G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 639 | chr1 | 84926046 | ||||||
chr1:84926215 | C | T | 1 | a0001c0001t0026 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 470 | chr1 | 84926215 | ||||||
chr1:84926338 | C | T | 1 | a0001c0001t0021 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 347 | chr1 | 84926338 | ||||||
chr1:84926374 | G | A | 4 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0029 others(1): Show |
6 | HG00280.hp1 HG01169.hp1 HG01257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*311C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 311 | chr1 | 84926374 | ||||||
chr1:84926381 | C | G | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0025 |
3 | HG01993.hp2 HG02647.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 304 | chr1 | 84926381 | ||||||
chr1:84926478 | A | G | 1 | a0005c0006t0024 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 207 | chr1 | 84926478 | ||||||
chr1:84926641 | C | T | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(14): Show |
93 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*44G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 14/14 | 44 | chr1 | 84926641 | ||||||
chr1:84996899 | C | G | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(13): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 27 | chr1 | 84996899 | ||||||
chr1:84996969 | G | T | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(13): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
5_prime_UTR_variant | MODIFIER | c.-97C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 97 | chr1 | 84996969 | ||||||
chr1:84996982 | T | G | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(13): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
5_prime_UTR_variant | MODIFIER | c.-110A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 110 | chr1 | 84996982 | ||||||
chr1:84997067 | T | C | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
5_prime_UTR_variant | MODIFIER | c.-195A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 195 | chr1 | 84997067 | ||||||
chr1:84997089 | G | C | 1 | a0001c0001t0010 | 5 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-217C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/14 | 217 | chr1 | 84997089 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84926933 | A | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0067 others(144): Show |
157 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1665-212T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84926933 | |||||||
chr1:84926977 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1665-256C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84926977 | |||||||
chr1:84927043 | G | A | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1665-322C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927043 | |||||||
chr1:84927157 | T | G | 21 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0002g0320 others(18): Show |
21 | HG00558.hp1 HG00609.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1665-436A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927157 | |||||||
chr1:84927192 | T | C | 1 | a0001c0001t0002g0309 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1665-471A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927192 | |||||||
chr1:84927192 | T | G | 11 | a0001c0001t0002g0306 a0001c0001t0005g0036 a0002c0002t0001g0055 others(8): Show |
11 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1665-471A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927192 | |||||||
chr1:84927204 | TA | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
173 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1665-484delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927204 | |||||||
chr1:84927205 | A | T | 3 | a0002c0002t0001g0060 a0002c0002t0002g0010 a0002c0002t0002g0236 |
4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1665-484T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927205 | |||||||
chr1:84927228 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1665-507A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927228 | |||||||
chr1:84927271 | T | TG | 6 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0012g0217 others(3): Show |
6 | HG00673.hp2 NA18612.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665-551dupC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927271 | |||||||
chr1:84927347 | T | A | 1 | a0001c0001t0007g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1665-626A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927347 | |||||||
chr1:84927489 | A | T | 12 | a0001c0001t0001g0077 a0001c0001t0002g0242 a0001c0001t0002g0274 others(9): Show |
14 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1665-768T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927489 | |||||||
chr1:84927498 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1665-777C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927498 | |||||||
chr1:84927752 | T | C | 1 | a0001c0001t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1665-1031A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927752 | |||||||
chr1:84927788 | T | G | 1 | a0001c0001t0014g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1665-1067A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927788 | |||||||
chr1:84927809 | G | A | 15 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0078 others(12): Show |
17 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1665-1088C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84927809 | |||||||
chr1:84928465 | T | C | 79 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(76): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1664+1093A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928465 | |||||||
chr1:84928525 | T | G | 5 | a0001c0001t0001g0084 a0001c0001t0003g0214 a0001c0001t0004g0099 others(2): Show |
5 | HG01074.hp1 HG01175.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664+1033A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928525 | |||||||
chr1:84928575 | T | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0112 others(32): Show |
37 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1664+983A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928575 | |||||||
chr1:84928603 | T | C | 8 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0026 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1664+955A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928603 | |||||||
chr1:84928622 | A | G | 7 | a0001c0001t0001g0069 a0001c0001t0001g0123 a0001c0001t0004g0082 others(4): Show |
7 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1664+936T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928622 | |||||||
chr1:84928665 | A | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1664+893T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928665 | |||||||
chr1:84928683 | A | C | 60 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(57): Show |
60 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1664+875T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928683 | |||||||
chr1:84928723 | T | A | 1 | a0001c0001t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1664+835A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928723 | |||||||
chr1:84928815 | T | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(75): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1664+743A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928815 | |||||||
chr1:84928942 | T | G | 2 | a0001c0001t0004g0094 a0001c0001t0012g0256 |
2 | NA18999.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1664+616A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84928942 | |||||||
chr1:84929041 | G | C | 1 | a0001c0001t0004g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1664+517C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929041 | |||||||
chr1:84929064 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(2): Show |
5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1664+494G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929064 | |||||||
chr1:84929340 | A | G | 1 | a0001c0001t0003g0321 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1664+218T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929340 | |||||||
chr1:84929361 | G | A | 1 | a0002c0002t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1664+197C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 13/13 | chr1 | 84929361 | |||||||
chr1:84929788 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1543-109T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929788 | |||||||
chr1:84929933 | T | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(169): Show |
177 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1543-254A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929933 | |||||||
chr1:84929933 | T | TA | 9 | a0002c0002t0001g0063 a0002c0002t0001g0068 a0002c0002t0001g0124 others(6): Show |
9 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1543-255dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929933 | |||||||
chr1:84929933 | T | TAA | 15 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0078 others(12): Show |
17 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1543-256_1543-255d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929933 | |||||||
chr1:84929934 | A | T | 9 | a0001c0001t0001g0164 a0001c0001t0002g0255 a0001c0001t0004g0150 others(6): Show |
11 | HG01928.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1543-255T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929934 | |||||||
chr1:84929937 | A | G | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1543-258T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84929937 | |||||||
chr1:84930042 | C | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0064 others(21): Show |
25 | HG01981.hp1 HG01993.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1543-363G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930042 | |||||||
chr1:84930139 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1543-460A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930139 | |||||||
chr1:84930178 | G | A | 16 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(13): Show |
18 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1543-499C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930178 | |||||||
chr1:84930269 | T | A | 30 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(27): Show |
31 | HG00280.hp2 HG00741.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1543-590A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930269 | |||||||
chr1:84930269 | T | TA | 11 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0034 others(8): Show |
11 | HG00741.hp2 HG01099.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1543-591dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930269 | |||||||
chr1:84930269 | TA | T | 11 | a0001c0001t0002g0226 a0001c0001t0005g0040 a0003c0003t0001g0087 others(8): Show |
12 | HG00642.hp2 HG01884.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1543-591delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930269 | |||||||
chr1:84930270 | A | T | 2 | a0001c0001t0001g0056 a0001c0001t0018g0225 |
2 | HG03017.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-591T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930270 | |||||||
chr1:84930337 | C | G | 2 | a0001c0001t0002g0317 a0004c0004t0001g0042 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1543-658G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930337 | |||||||
chr1:84930348 | T | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0112 others(33): Show |
38 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.1543-669A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930348 | |||||||
chr1:84930357 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1543-678A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930357 | |||||||
chr1:84930456 | C | T | 1 | a0001c0001t0010g0333 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1543-777G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930456 | |||||||
chr1:84930475 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(216): Show |
227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1543-796A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930475 | |||||||
chr1:84930511 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1543-832C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930511 | |||||||
chr1:84930759 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1542+603C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930759 | |||||||
chr1:84930907 | A | T | 6 | a0001c0001t0002g0306 a0001c0001t0002g0317 a0001c0001t0002g0318 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+455T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930907 | |||||||
chr1:84930953 | T | C | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+409A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930953 | |||||||
chr1:84930975 | T | C | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+387A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84930975 | |||||||
chr1:84931012 | C | T | 10 | a0001c0001t0005g0040 a0003c0003t0001g0087 a0003c0003t0001g0097 others(7): Show |
11 | HG00642.hp2 HG01884.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542+350G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931012 | |||||||
chr1:84931038 | T | G | 1 | a0001c0001t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1542+324A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931038 | |||||||
chr1:84931095 | A | G | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1542+267T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931095 | |||||||
chr1:84931115 | A | ACTTACCC others(13): Show |
1 | a0001c0001t0007g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1542+227_1542+246d others(22): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931115 | |||||||
chr1:84931117 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0064 others(30): Show |
34 | HG00639.hp2 HG01981.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.1542+245A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931117 | |||||||
chr1:84931207 | A | G | 1 | a0001c0001t0002g0212 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1542+155T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 12/13 | chr1 | 84931207 | |||||||
chr1:84931603 | G | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(75): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-35C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84931603 | |||||||
chr1:84931650 | A | G | 8 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0026 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336-82T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84931650 | |||||||
chr1:84932010 | C | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336-442G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932010 | |||||||
chr1:84932029 | A | AAC | 28 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0067 others(25): Show |
31 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-463_1336-462d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | |||||||
chr1:84932029 | A | AACAC | 9 | a0001c0001t0001g0064 a0001c0001t0001g0121 a0001c0001t0001g0125 others(6): Show |
9 | HG02055.hp1 HG02965.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1336-465_1336-462d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | |||||||
chr1:84932029 | A | AACACAC | 6 | a0002c0002t0001g0055 a0002c0002t0001g0124 a0002c0002t0027g0107 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-467_1336-462d others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | |||||||
chr1:84932029 | AAC | A | 83 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(80): Show |
84 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1336-463_1336-462d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932029 | |||||||
chr1:84932439 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1336-871G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932439 | |||||||
chr1:84932592 | CT | C | 21 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(18): Show |
24 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1336-1025delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932592 | |||||||
chr1:84932651 | T | C | 23 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(20): Show |
26 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1336-1083A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932651 | |||||||
chr1:84932874 | C | G | 1 | a0001c0001t0007g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1336-1306G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84932874 | |||||||
chr1:84933024 | T | C | 1 | a0001c0001t0008g0267 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1336-1456A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933024 | |||||||
chr1:84933089 | C | A | 9 | a0002c0002t0001g0055 a0002c0002t0001g0063 a0002c0002t0001g0068 others(6): Show |
9 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1336-1521G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933089 | |||||||
chr1:84933296 | C | T | 4 | a0001c0001t0002g0306 a0001c0001t0002g0318 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-1728G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933296 | |||||||
chr1:84933370 | C | T | 3 | a0002c0002t0001g0060 a0002c0002t0002g0010 a0002c0002t0002g0236 |
4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-1802G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933370 | |||||||
chr1:84933533 | T | C | 3 | a0001c0001t0002g0231 a0001c0001t0002g0317 a0004c0004t0001g0042 |
3 | HG02258.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1336-1965A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933533 | |||||||
chr1:84933545 | G | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(218): Show |
229 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1336-1977C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933545 | |||||||
chr1:84933649 | C | T | 1 | a0001c0001t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336-2081G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933649 | |||||||
chr1:84933684 | T | C | 1 | a0001c0001t0003g0257 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1336-2116A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933684 | |||||||
chr1:84933744 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1336-2176A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933744 | |||||||
chr1:84933802 | A | G | 4 | a0001c0001t0002g0306 a0001c0001t0002g0318 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-2234T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933802 | |||||||
chr1:84933927 | C | A | 8 | a0003c0003t0001g0087 a0003c0003t0001g0097 a0003c0003t0005g0002 others(5): Show |
9 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1336-2359G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84933927 | |||||||
chr1:84934076 | T | C | 1 | a0001c0001t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336-2508A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934076 | |||||||
chr1:84934098 | A | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(75): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-2530T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934098 | |||||||
chr1:84934157 | A | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(75): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-2589T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934157 | |||||||
chr1:84934317 | TCCATAAA others(6): Show |
T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(178): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1336-2762_1336-275 others(17): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934317 | |||||||
chr1:84934343 | T | C | 4 | a0001c0001t0002g0306 a0001c0001t0002g0318 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-2775A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934343 | |||||||
chr1:84934383 | A | G | 1 | a0001c0001t0003g0264 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1336-2815T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934383 | |||||||
chr1:84934431 | C | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(82): Show |
86 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1336-2863G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934431 | |||||||
chr1:84934499 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(174): Show |
182 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1336-2931G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934499 | |||||||
chr1:84934574 | GCA | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(75): Show |
81 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1336-3008_1336-300 others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934574 | |||||||
chr1:84934718 | C | T | 1 | a0001c0001t0003g0205 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1335+3037G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934718 | |||||||
chr1:84934880 | T | C | 8 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0026 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335+2875A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84934880 | |||||||
chr1:84935055 | C | T | 3 | a0002c0002t0001g0060 a0002c0002t0002g0010 a0002c0002t0002g0236 |
4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+2700G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935055 | |||||||
chr1:84935152 | T | C | 6 | a0001c0001t0002g0306 a0001c0001t0002g0317 a0001c0001t0002g0318 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335+2603A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935152 | |||||||
chr1:84935155 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1335+2600C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935155 | |||||||
chr1:84935210 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1335+2545G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935210 | |||||||
chr1:84935233 | A | C | 1 | a0001c0001t0003g0214 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1335+2522T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935233 | |||||||
chr1:84935252 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0059 others(137): Show |
143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1335+2503G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935252 | |||||||
chr1:84935363 | A | C | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1335+2392T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935363 | |||||||
chr1:84935426 | A | C | 1 | a0001c0001t0007g0171 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1335+2329T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935426 | |||||||
chr1:84935799 | T | C | 16 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(13): Show |
18 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1335+1956A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935799 | |||||||
chr1:84935842 | T | G | 2 | a0001c0001t0001g0177 a0001c0001t0028g0135 |
2 | NA18968.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1335+1913A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935842 | |||||||
chr1:84935880 | T | G | 1 | a0001c0001t0006g0279 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1335+1875A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84935880 | |||||||
chr1:84936033 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1335+1722G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936033 | |||||||
chr1:84936035 | G | T | 62 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(59): Show |
62 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1335+1720C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936035 | |||||||
chr1:84936110 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1335+1645G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936110 | |||||||
chr1:84936187 | G | C | 1 | a0004c0004t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1335+1568C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936187 | |||||||
chr1:84936559 | A | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(76): Show |
82 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1335+1196T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936559 | |||||||
chr1:84936561 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1335+1194T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936561 | |||||||
chr1:84936790 | A | G | 1 | a0001c0001t0025g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1335+965T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936790 | |||||||
chr1:84936806 | C | T | 1 | a0001c0001t0003g0310 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1335+949G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936806 | |||||||
chr1:84936961 | C | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0092 others(34): Show |
39 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.1335+794G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84936961 | |||||||
chr1:84937189 | C | T | 1 | a0001c0001t0005g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1335+566G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937189 | |||||||
chr1:84937250 | A | G | 1 | a0001c0001t0007g0117 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1335+505T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937250 | |||||||
chr1:84937283 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1335+472C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937283 | |||||||
chr1:84937314 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(102): Show |
109 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1335+441T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937314 | |||||||
chr1:84937429 | C | T | 3 | a0002c0002t0001g0060 a0002c0002t0002g0010 a0002c0002t0002g0236 |
4 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+326G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937429 | |||||||
chr1:84937462 | C | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(210): Show |
219 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.1335+293G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937462 | |||||||
chr1:84937491 | C | T | 1 | a0002c0002t0027g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1335+264G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937491 | |||||||
chr1:84937492 | G | A | 8 | a0003c0003t0001g0087 a0003c0003t0001g0097 a0003c0003t0005g0002 others(5): Show |
9 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+263C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937492 | |||||||
chr1:84937542 | T | C | 2 | a0001c0001t0002g0323 a0001c0001t0002g0327 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1335+213A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937542 | |||||||
chr1:84937661 | G | A | 1 | a0001c0001t0002g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1335+94C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 11/13 | chr1 | 84937661 | |||||||
chr1:84937887 | A | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1213-10T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 10/13 | chr1 | 84937887 | |||||||
chr1:84938672 | C | T | 8 | a0001c0001t0002g0212 a0001c0001t0006g0232 a0001c0001t0006g0284 others(5): Show |
8 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-590G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84938672 | |||||||
chr1:84939007 | G | T | 1 | a0003c0003t0001g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1110+546C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939007 | |||||||
chr1:84939078 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA18964.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1110+475C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939078 | |||||||
chr1:84939115 | T | G | 1 | a0001c0001t0017g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1110+438A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939115 | |||||||
chr1:84939543 | C | T | 8 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0026 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+10G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 9/13 | chr1 | 84939543 | |||||||
chr1:84939706 | T | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0064 others(21): Show |
25 | HG01981.hp1 HG01993.hp1 HG02055.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.961-4A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84939706 | |||||||
chr1:84939911 | T | G | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-209A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84939911 | |||||||
chr1:84940003 | C | T | 7 | a0003c0003t0001g0097 a0003c0003t0005g0002 a0003c0003t0005g0030 others(4): Show |
8 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-301G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940003 | |||||||
chr1:84940007 | A | G | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-305T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940007 | |||||||
chr1:84940041 | C | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.961-339G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940041 | |||||||
chr1:84940101 | C | T | 18 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(15): Show |
18 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-399G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940101 | |||||||
chr1:84940102 | G | A | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-400C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940102 | |||||||
chr1:84940156 | C | G | 2 | a0005c0006t0001g0132 a0005c0006t0024g0133 |
2 | HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-454G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940156 | |||||||
chr1:84940204 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0054 others(152): Show |
163 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.961-502T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940204 | |||||||
chr1:84940211 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0081 others(74): Show |
80 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.961-509T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940211 | |||||||
chr1:84940360 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.960+519A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940360 | |||||||
chr1:84940390 | C | A | 1 | a0001c0001t0002g0324 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+489G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 8/13 | chr1 | 84940390 | |||||||
chr1:84941100 | G | C | 1 | a0001c0001t0003g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.848-109C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941100 | |||||||
chr1:84941119 | T | C | 8 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0026 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-128A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941119 | |||||||
chr1:84941268 | G | C | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.848-277C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941268 | |||||||
chr1:84941278 | C | T | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.848-287G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941278 | |||||||
chr1:84941307 | T | C | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.848-316A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941307 | |||||||
chr1:84941315 | T | C | 18 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(15): Show |
21 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.848-324A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941315 | |||||||
chr1:84941369 | C | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0064 others(31): Show |
35 | HG01981.hp1 HG01993.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.848-378G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941369 | |||||||
chr1:84941415 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848-424A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941415 | |||||||
chr1:84941461 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
191 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.848-470G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941461 | |||||||
chr1:84941462 | G | A | 1 | a0001c0001t0007g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.848-471C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941462 | |||||||
chr1:84941501 | C | CA | 9 | a0002c0002t0001g0055 a0002c0002t0001g0063 a0002c0002t0001g0068 others(6): Show |
9 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-511dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941501 | |||||||
chr1:84941508 | C | G | 1 | a0001c0001t0002g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.848-517G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941508 | |||||||
chr1:84941565 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
207 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.848-574A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941565 | |||||||
chr1:84941774 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.848-783G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941774 | |||||||
chr1:84941926 | T | C | 12 | a0001c0001t0001g0092 a0001c0001t0001g0112 a0001c0001t0002g0191 others(9): Show |
12 | HG00323.hp1 HG01106.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.848-935A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941926 | |||||||
chr1:84941963 | C | G | 3 | a0006c0005t0001g0044 a0006c0005t0001g0045 a0006c0005t0001g0047 |
3 | HG02615.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.848-972G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941963 | |||||||
chr1:84941965 | C | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(15): Show |
21 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.848-974G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941965 | |||||||
chr1:84941966 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
207 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.848-975T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84941966 | |||||||
chr1:84942061 | T | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0160 a0001c0001t0001g0163 |
3 | HG01243.hp1 NA18943.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.848-1070A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942061 | |||||||
chr1:84942180 | A | G | 39 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(36): Show |
42 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.848-1189T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942180 | |||||||
chr1:84942280 | C | T | 1 | a0001c0001t0022g0144 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.848-1289G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942280 | |||||||
chr1:84942303 | G | C | 61 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(58): Show |
61 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.848-1312C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942303 | |||||||
chr1:84942348 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.848-1357G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942348 | |||||||
chr1:84942447 | G | A | 1 | a0001c0001t0005g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.848-1456C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942447 | |||||||
chr1:84942583 | TC | T | 62 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(59): Show |
62 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.848-1593delG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942583 | |||||||
chr1:84942641 | G | A | 62 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(59): Show |
62 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.848-1650C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942641 | |||||||
chr1:84942849 | AC | A | 9 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0005g0026 others(6): Show |
9 | HG00642.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.848-1859delG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942849 | |||||||
chr1:84942933 | G | T | 50 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(47): Show |
50 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.848-1942C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84942933 | |||||||
chr1:84943353 | T | G | 114 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(111): Show |
116 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.848-2362A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943353 | |||||||
chr1:84943372 | G | A | 23 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(20): Show |
26 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.848-2381C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943372 | |||||||
chr1:84943508 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.848-2517C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943508 | |||||||
chr1:84943582 | CCA | C | 10 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0002g0317 others(7): Show |
10 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.848-2593_848-2592d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943582 | |||||||
chr1:84943670 | G | A | 1 | a0001c0001t0007g0117 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.848-2679C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84943670 | |||||||
chr1:84944261 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.847+2772C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944261 | |||||||
chr1:84944347 | A | G | 8 | a0001c0001t0005g0040 a0003c0003t0001g0097 a0003c0003t0005g0002 others(5): Show |
9 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+2686T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944347 | |||||||
chr1:84944378 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0174 a0001c0001t0004g0148 |
3 | HG00558.hp2 NA18960.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.847+2655G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944378 | |||||||
chr1:84944389 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.847+2644G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944389 | |||||||
chr1:84944392 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.847+2641C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944392 | |||||||
chr1:84944479 | G | GC | 14 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+2553dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944479 | |||||||
chr1:84944533 | A | AAAAG | 8 | a0001c0001t0001g0164 a0001c0001t0004g0150 a0001c0001t0006g0014 others(5): Show |
10 | HG01928.hp1 HG01943.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.847+2496_847+2499d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944533 | |||||||
chr1:84944533 | A | G | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.847+2500T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944533 | |||||||
chr1:84944533 | AAAAG | A | 14 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+2496_847+2499d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944533 | |||||||
chr1:84944559 | A | G | 32 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(29): Show |
35 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.847+2474T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944559 | |||||||
chr1:84944591 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.847+2442G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944591 | |||||||
chr1:84944608 | C | T | 2 | a0001c0001t0002g0203 a0001c0001t0003g0205 |
2 | HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.847+2425G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944608 | |||||||
chr1:84944657 | C | T | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.847+2376G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944657 | |||||||
chr1:84944857 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.847+2176T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944857 | |||||||
chr1:84944861 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(79): Show |
83 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+2172G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84944861 | |||||||
chr1:84945071 | TA | T | 55 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(52): Show |
59 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.847+1961delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945071 | |||||||
chr1:84945136 | T | C | 1 | a0001c0001t0003g0240 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.847+1897A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945136 | |||||||
chr1:84945366 | T | TC | 18 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(15): Show |
21 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+1666dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945366 | |||||||
chr1:84945674 | T | C | 14 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+1359A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945674 | |||||||
chr1:84945748 | T | C | 9 | a0002c0002t0001g0055 a0002c0002t0001g0063 a0002c0002t0001g0068 others(6): Show |
9 | HG00639.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.847+1285A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84945748 | |||||||
chr1:84946002 | G | A | 14 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+1031C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946002 | |||||||
chr1:84946038 | T | C | 14 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+995A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946038 | |||||||
chr1:84946123 | C | T | 1 | a0001c0001t0003g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.847+910G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946123 | |||||||
chr1:84946320 | G | A | 1 | a0002c0002t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.847+713C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946320 | |||||||
chr1:84946448 | A | G | 14 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(11): Show |
15 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.847+585T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946448 | |||||||
chr1:84946464 | T | C | 1 | a0001c0001t0003g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.847+569A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946464 | |||||||
chr1:84946482 | T | A | 2 | a0001c0001t0001g0168 a0001c0001t0002g0280 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.847+551A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946482 | |||||||
chr1:84946607 | T | C | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+426A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946607 | |||||||
chr1:84946753 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(79): Show |
83 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+280G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946753 | |||||||
chr1:84946778 | C | T | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+255G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946778 | |||||||
chr1:84946940 | T | C | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+93A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 7/13 | chr1 | 84946940 | |||||||
chr1:84947306 | C | CCACA | 16 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(13): Show |
18 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.748-178_748-175dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947306 | |||||||
chr1:84947306 | C | CCACACA | 11 | a0002c0002t0001g0055 a0002c0002t0001g0060 a0002c0002t0001g0063 others(8): Show |
12 | HG01167.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-180_748-175dup others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947306 | |||||||
chr1:84947306 | CCA | C | 24 | a0001c0001t0002g0198 a0001c0001t0002g0231 a0001c0001t0002g0247 others(21): Show |
25 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.748-176_748-175del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947306 | |||||||
chr1:84947329 | C | A | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-197G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947329 | |||||||
chr1:84947329 | C | CACACAT | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.748-198_748-197ins others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947329 | |||||||
chr1:84947518 | A | G | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-386T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947518 | |||||||
chr1:84947592 | C | A | 47 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(44): Show |
51 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.748-460G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947592 | |||||||
chr1:84947651 | G | A | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-519C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947651 | |||||||
chr1:84947673 | C | T | 2 | a0003c0003t0001g0097 a0003c0003t0013g0027 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.748-541G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947673 | |||||||
chr1:84947697 | G | A | 36 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(33): Show |
40 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.748-565C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947697 | |||||||
chr1:84947793 | TTG | T | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-663_748-662del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947793 | |||||||
chr1:84947964 | G | C | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-832C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84947964 | |||||||
chr1:84948082 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(134): Show |
142 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.748-950A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948082 | |||||||
chr1:84948223 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.748-1091G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948223 | |||||||
chr1:84948308 | C | T | 19 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(16): Show |
22 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.748-1176G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948308 | |||||||
chr1:84948403 | A | C | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1271T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948403 | |||||||
chr1:84948428 | T | C | 3 | a0005c0006t0001g0132 a0005c0006t0003g0325 a0005c0006t0024g0133 |
3 | HG00741.hp2 HG01099.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.748-1296A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948428 | |||||||
chr1:84948440 | T | G | 10 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0002g0317 others(7): Show |
10 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-1308A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948440 | |||||||
chr1:84948445 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.748-1313G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948445 | |||||||
chr1:84948464 | T | C | 11 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-1332A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948464 | |||||||
chr1:84948583 | A | G | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1451T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948583 | |||||||
chr1:84948853 | C | T | 11 | a0001c0001t0002g0231 a0001c0001t0002g0247 a0001c0001t0002g0294 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.748-1721G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948853 | |||||||
chr1:84948854 | G | A | 1 | a0003c0003t0001g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.748-1722C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84948854 | |||||||
chr1:84949001 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.748-1869C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949001 | |||||||
chr1:84949008 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(134): Show |
142 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.748-1876G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949008 | |||||||
chr1:84949010 | A | T | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.748-1878T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949010 | |||||||
chr1:84949044 | C | T | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.748-1912G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949044 | |||||||
chr1:84949091 | C | G | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1959G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949091 | |||||||
chr1:84949130 | G | A | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.748-1998C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949130 | |||||||
chr1:84949157 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.748-2025T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949157 | |||||||
chr1:84949157 | A | T | 10 | a0001c0001t0002g0247 a0001c0001t0002g0294 a0001c0001t0002g0317 others(7): Show |
10 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-2025T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949157 | |||||||
chr1:84949335 | G | A | 47 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(44): Show |
51 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.748-2203C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949335 | |||||||
chr1:84949361 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0004c0004t0001g0041 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2229C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949361 | |||||||
chr1:84949366 | C | T | 5 | a0001c0001t0005g0021 a0001c0001t0005g0025 a0001c0001t0014g0017 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-2234G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949366 | |||||||
chr1:84949421 | G | A | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-2289C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949421 | |||||||
chr1:84949455 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(87): Show |
91 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.748-2323C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949455 | |||||||
chr1:84949482 | C | CA | 5 | a0001c0001t0001g0084 a0001c0001t0003g0214 a0001c0001t0004g0099 others(2): Show |
5 | HG01074.hp1 HG01175.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2351dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949482 | |||||||
chr1:84949482 | CA | C | 12 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(9): Show |
13 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-2351delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949482 | |||||||
chr1:84949497 | T | C | 55 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(52): Show |
59 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.748-2365A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949497 | |||||||
chr1:84949747 | G | T | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+2496C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84949747 | |||||||
chr1:84950030 | T | C | 1 | a0001c0001t0006g0285 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.747+2213A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950030 | |||||||
chr1:84950115 | A | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0059 others(87): Show |
91 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.747+2128T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950115 | |||||||
chr1:84950389 | A | C | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+1854T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950389 | |||||||
chr1:84950405 | T | G | 1 | a0001c0001t0008g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.747+1838A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950405 | |||||||
chr1:84950506 | T | C | 13 | a0001c0001t0002g0231 a0001c0001t0002g0306 a0001c0001t0005g0040 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+1737A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950506 | |||||||
chr1:84950928 | A | C | 29 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(26): Show |
32 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.747+1315T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950928 | |||||||
chr1:84950931 | A | G | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.747+1312T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84950931 | |||||||
chr1:84951113 | C | T | 64 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(61): Show |
68 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.747+1130G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951113 | |||||||
chr1:84951157 | C | T | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0017g0103 others(1): Show |
4 | HG00280.hp1 HG00735.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+1086G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951157 | |||||||
chr1:84951158 | G | A | 70 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0066 others(67): Show |
73 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.747+1085C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951158 | |||||||
chr1:84951166 | G | A | 8 | a0003c0003t0001g0097 a0003c0003t0005g0002 a0003c0003t0005g0030 others(5): Show |
9 | HG00642.hp2 HG01884.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.747+1077C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951166 | |||||||
chr1:84951516 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.747+727T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951516 | |||||||
chr1:84951695 | T | C | 36 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(33): Show |
37 | HG00639.hp2 HG01884.hp2 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.747+548A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951695 | |||||||
chr1:84951844 | A | G | 37 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(34): Show |
38 | HG01884.hp2 HG01981.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.747+399T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951844 | |||||||
chr1:84951845 | G | A | 37 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(34): Show |
38 | HG01884.hp2 HG01981.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.747+398C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951845 | |||||||
chr1:84951863 | A | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0059 others(84): Show |
89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.747+380T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951863 | |||||||
chr1:84951867 | G | A | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.747+376C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951867 | |||||||
chr1:84951871 | G | A | 3 | a0002c0002t0001g0124 a0004c0004t0001g0046 a0006c0005t0001g0047 |
3 | HG02615.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.747+372C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951871 | |||||||
chr1:84951965 | T | C | 2 | a0001c0001t0031g0246 a0007c0010t0002g0245 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.747+278A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84951965 | |||||||
chr1:84952002 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.747+241C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952002 | |||||||
chr1:84952052 | A | T | 1 | a0001c0001t0005g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.747+191T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952052 | |||||||
chr1:84952081 | T | C | 42 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(39): Show |
43 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.747+162A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952081 | |||||||
chr1:84952096 | G | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0059 others(188): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.747+147C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952096 | |||||||
chr1:84952136 | A | C | 29 | a0001c0001t0002g0294 a0001c0001t0005g0019 a0001c0001t0005g0021 others(26): Show |
30 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.747+107T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 6/13 | chr1 | 84952136 | |||||||
chr1:84952624 | C | G | 197 | a0001c0001t0001g0056 a0001c0001t0001g0086 a0001c0001t0002g0015 others(194): Show |
207 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.566-94G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952624 | |||||||
chr1:84952658 | G | C | 28 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(25): Show |
29 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.566-128C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952658 | |||||||
chr1:84952726 | T | C | 1 | a0001c0001t0003g0214 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.566-196A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952726 | |||||||
chr1:84952962 | A | G | 32 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(29): Show |
33 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-432T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84952962 | |||||||
chr1:84953273 | C | T | 27 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(24): Show |
28 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-743G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953273 | |||||||
chr1:84953274 | A | G | 33 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(30): Show |
34 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.566-744T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953274 | |||||||
chr1:84953376 | G | A | 33 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(30): Show |
35 | HG00597.hp1 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.566-846C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953376 | |||||||
chr1:84953407 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.566-877C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953407 | |||||||
chr1:84953448 | G | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.566-918C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953448 | |||||||
chr1:84953529 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.566-999C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953529 | |||||||
chr1:84953550 | C | CA | 7 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(4): Show |
7 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-1021dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953550 | |||||||
chr1:84953550 | CA | C | 130 | a0001c0001t0001g0140 a0001c0001t0002g0015 a0001c0001t0002g0189 others(127): Show |
138 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.566-1021delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953550 | |||||||
chr1:84953550 | CAAAA | C | 31 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(28): Show |
32 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-1024_566-1021d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953550 | |||||||
chr1:84953568 | AT | A | 26 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(23): Show |
27 | HG01243.hp2 HG02015.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.566-1039delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953568 | |||||||
chr1:84953569 | T | A | 3 | a0001c0001t0001g0120 a0001c0001t0007g0119 a0001c0001t0020g0090 |
3 | HG01993.hp2 NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.566-1039A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953569 | |||||||
chr1:84953592 | T | A | 7 | a0001c0001t0002g0201 a0001c0001t0002g0203 a0001c0001t0003g0187 others(4): Show |
7 | HG00639.hp1 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-1062A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953592 | |||||||
chr1:84953637 | G | A | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.566-1107C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953637 | |||||||
chr1:84953641 | G | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.566-1111C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953641 | |||||||
chr1:84953668 | T | C | 5 | a0002c0002t0001g0124 a0004c0004t0001g0046 a0006c0005t0001g0044 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-1138A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953668 | |||||||
chr1:84953694 | T | C | 1 | a0001c0001t0007g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.566-1164A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953694 | |||||||
chr1:84953702 | A | C | 63 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(60): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.566-1172T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953702 | |||||||
chr1:84953705 | A | G | 63 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(60): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.566-1175T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953705 | |||||||
chr1:84953706 | C | CTCA | 63 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(60): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.566-1177_566-1176i others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953706 | |||||||
chr1:84953708 | G | T | 32 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(29): Show |
33 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-1178C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953708 | |||||||
chr1:84953952 | G | C | 1 | a0001c0001t0002g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.566-1422C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953952 | |||||||
chr1:84953993 | A | G | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.566-1463T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84953993 | |||||||
chr1:84954230 | C | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-1700G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954230 | |||||||
chr1:84954264 | T | C | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.566-1734A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954264 | |||||||
chr1:84954361 | A | C | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.566-1831T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954361 | |||||||
chr1:84954665 | G | A | 11 | a0001c0001t0002g0242 a0001c0001t0002g0247 a0001c0001t0003g0008 others(8): Show |
14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.565+1766C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954665 | |||||||
chr1:84954810 | C | T | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.565+1621G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84954810 | |||||||
chr1:84955005 | C | A | 1 | a0001c0001t0004g0139 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.565+1426G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955005 | |||||||
chr1:84955094 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.565+1337G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955094 | |||||||
chr1:84955189 | T | C | 9 | a0002c0002t0001g0124 a0004c0004t0001g0041 a0004c0004t0001g0042 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+1242A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955189 | |||||||
chr1:84955305 | C | T | 1 | a0001c0001t0012g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.565+1126G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955305 | |||||||
chr1:84955348 | A | G | 1 | a0001c0001t0031g0246 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.565+1083T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955348 | |||||||
chr1:84955359 | G | A | 125 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(122): Show |
130 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.565+1072C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955359 | |||||||
chr1:84955448 | T | A | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.565+983A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955448 | |||||||
chr1:84955484 | G | A | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.565+947C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955484 | |||||||
chr1:84955543 | G | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.565+888C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955543 | |||||||
chr1:84955644 | C | T | 54 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(51): Show |
55 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.565+787G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955644 | |||||||
chr1:84955702 | C | T | 1 | a0006c0005t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.565+729G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955702 | |||||||
chr1:84955954 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.565+477T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84955954 | |||||||
chr1:84956112 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+319A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956112 | |||||||
chr1:84956154 | G | GAA | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.565+275_565+276dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956154 | |||||||
chr1:84956160 | A | G | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.565+271T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956160 | |||||||
chr1:84956215 | C | T | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.565+216G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956215 | |||||||
chr1:84956378 | C | T | 195 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(192): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.565+53G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 4/13 | chr1 | 84956378 | |||||||
chr1:84956695 | T | C | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.412-111A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956695 | |||||||
chr1:84956723 | C | A | 1 | a0001c0001t0002g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.412-139G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956723 | |||||||
chr1:84956869 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.412-285G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956869 | |||||||
chr1:84956951 | C | T | 27 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(24): Show |
28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.412-367G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956951 | |||||||
chr1:84956979 | G | T | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.412-395C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84956979 | |||||||
chr1:84957091 | C | T | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-507G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957091 | |||||||
chr1:84957125 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.412-541T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957125 | |||||||
chr1:84957537 | T | C | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.412-953A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957537 | |||||||
chr1:84957581 | A | G | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.411+948T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957581 | |||||||
chr1:84957792 | G | T | 3 | a0001c0001t0001g0134 a0005c0006t0001g0132 a0005c0006t0024g0133 |
3 | HG01099.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.411+737C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957792 | |||||||
chr1:84957831 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.411+698C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957831 | |||||||
chr1:84957858 | A | T | 128 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(125): Show |
134 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.411+671T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84957858 | |||||||
chr1:84958037 | T | C | 92 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(89): Show |
97 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.411+492A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958037 | |||||||
chr1:84958062 | C | G | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.411+467G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958062 | |||||||
chr1:84958131 | G | T | 1 | a0001c0001t0003g0283 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.411+398C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958131 | |||||||
chr1:84958198 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.411+331G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958198 | |||||||
chr1:84958499 | A | G | 127 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(124): Show |
133 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.411+30T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 3/13 | chr1 | 84958499 | |||||||
chr1:84958796 | A | G | 127 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(124): Show |
133 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.238-94T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958796 | |||||||
chr1:84958830 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0122 others(1): Show |
4 | HG02630.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-128G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958830 | |||||||
chr1:84958897 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.238-195G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958897 | |||||||
chr1:84958914 | A | T | 127 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(124): Show |
133 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.238-212T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958914 | |||||||
chr1:84958977 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238-275G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84958977 | |||||||
chr1:84959012 | T | G | 1 | a0001c0001t0003g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.238-310A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959012 | |||||||
chr1:84959187 | A | T | 1 | a0001c0001t0003g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.238-485T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959187 | |||||||
chr1:84959255 | A | G | 9 | a0002c0002t0001g0124 a0004c0004t0001g0041 a0004c0004t0001g0042 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-553T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959255 | |||||||
chr1:84959404 | G | A | 7 | a0001c0001t0002g0242 a0001c0001t0003g0008 a0001c0001t0003g0009 others(4): Show |
9 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.238-702C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959404 | |||||||
chr1:84959590 | T | G | 1 | a0004c0004t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-888A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959590 | |||||||
chr1:84959591 | C | A | 1 | a0004c0004t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-889G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959591 | |||||||
chr1:84959629 | G | A | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-927C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959629 | |||||||
chr1:84959646 | A | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238-944T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959646 | |||||||
chr1:84959746 | C | A | 1 | a0001c0001t0003g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.238-1044G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959746 | |||||||
chr1:84959864 | C | T | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238-1162G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84959864 | |||||||
chr1:84960023 | A | G | 195 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(192): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.238-1321T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960023 | |||||||
chr1:84960093 | C | T | 6 | a0001c0001t0002g0255 a0001c0001t0002g0281 a0001c0001t0002g0289 others(3): Show |
7 | HG01255.hp2 HG01358.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-1391G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960093 | |||||||
chr1:84960106 | G | T | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-1404C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960106 | |||||||
chr1:84960138 | T | C | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.238-1436A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960138 | |||||||
chr1:84960229 | C | T | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-1527G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960229 | |||||||
chr1:84960246 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0004g0093 a0001c0001t0004g0094 others(2): Show |
6 | HG00597.hp2 NA18964.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-1544C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960246 | |||||||
chr1:84960391 | T | C | 1 | a0001c0001t0002g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.238-1689A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960391 | |||||||
chr1:84960477 | G | T | 120 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(117): Show |
125 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.238-1775C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960477 | |||||||
chr1:84960573 | T | C | 27 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(24): Show |
28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.238-1871A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960573 | |||||||
chr1:84960689 | G | A | 4 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-1987C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960689 | |||||||
chr1:84960701 | G | A | 5 | a0002c0002t0001g0124 a0004c0004t0001g0046 a0006c0005t0001g0044 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-1999C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960701 | |||||||
chr1:84960739 | A | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238-2037T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960739 | |||||||
chr1:84960786 | A | G | 1 | a0001c0001t0003g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.238-2084T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960786 | |||||||
chr1:84960791 | T | C | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.238-2089A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960791 | |||||||
chr1:84960872 | T | G | 123 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(120): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.238-2170A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960872 | |||||||
chr1:84960879 | C | T | 4 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-2177G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960879 | |||||||
chr1:84960888 | G | GAAC | 123 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(120): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.238-2189_238-2187d others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960888 | |||||||
chr1:84960957 | T | C | 1 | a0001c0001t0008g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.238-2255A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960957 | |||||||
chr1:84960981 | C | A | 89 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(86): Show |
93 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.238-2279G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84960981 | |||||||
chr1:84961044 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.238-2342T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961044 | |||||||
chr1:84961124 | G | A | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-2422C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961124 | |||||||
chr1:84961190 | C | T | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238-2488G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961190 | |||||||
chr1:84961316 | T | C | 4 | a0001c0001t0002g0192 a0001c0001t0002g0294 a0001c0001t0031g0246 others(1): Show |
4 | HG00642.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-2614A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961316 | |||||||
chr1:84961633 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238-2931C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84961633 | |||||||
chr1:84962009 | C | T | 10 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.238-3307G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962009 | |||||||
chr1:84962099 | C | T | 4 | a0003c0003t0005g0030 a0003c0003t0005g0031 a0003c0003t0005g0032 others(1): Show |
4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-3397G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962099 | |||||||
chr1:84962656 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.237+2893G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962656 | |||||||
chr1:84962705 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.237+2844G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962705 | |||||||
chr1:84962708 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.237+2841C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962708 | |||||||
chr1:84962721 | A | G | 5 | a0002c0002t0001g0124 a0004c0004t0001g0046 a0006c0005t0001g0044 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+2828T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962721 | |||||||
chr1:84962933 | C | T | 1 | a0001c0001t0002g0298 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.237+2616G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84962933 | |||||||
chr1:84963437 | T | C | 27 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(24): Show |
28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.237+2112A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963437 | |||||||
chr1:84963507 | T | C | 1 | a0001c0001t0004g0148 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.237+2042A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963507 | |||||||
chr1:84963588 | T | C | 1 | a0001c0001t0003g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.237+1961A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963588 | |||||||
chr1:84963598 | G | T | 1 | a0003c0003t0013g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.237+1951C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963598 | |||||||
chr1:84963628 | T | C | 1 | a0001c0001t0004g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.237+1921A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963628 | |||||||
chr1:84963761 | A | G | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.237+1788T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963761 | |||||||
chr1:84963804 | T | C | 1 | a0001c0001t0002g0309 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.237+1745A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963804 | |||||||
chr1:84963901 | C | T | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.237+1648G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963901 | |||||||
chr1:84963912 | T | C | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.237+1637A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84963912 | |||||||
chr1:84964118 | A | G | 71 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(68): Show |
76 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.237+1431T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964118 | |||||||
chr1:84964207 | C | T | 120 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(117): Show |
125 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.237+1342G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964207 | |||||||
chr1:84964279 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.237+1270G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964279 | |||||||
chr1:84964303 | G | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0016g0128 others(2): Show |
5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1246C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964303 | |||||||
chr1:84964526 | T | TG | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
130 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.237+1022dupC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964526 | |||||||
chr1:84964527 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.237+1022C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964527 | |||||||
chr1:84964532 | G | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+1017C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964532 | |||||||
chr1:84964533 | G | GC | 3 | a0001c0001t0003g0013 a0001c0001t0003g0257 a0001c0001t0006g0285 |
4 | NA18970.hp1 NA18995.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+1015_237+1016i others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964533 | |||||||
chr1:84964681 | A | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.237+868T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964681 | |||||||
chr1:84964839 | G | A | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.237+710C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964839 | |||||||
chr1:84964875 | T | TA | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.237+673dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84964875 | |||||||
chr1:84965027 | A | G | 89 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(86): Show |
93 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.237+522T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84965027 | |||||||
chr1:84965168 | T | C | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.237+381A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84965168 | |||||||
chr1:84965192 | T | C | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.237+357A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 2/13 | chr1 | 84965192 | |||||||
chr1:84965809 | G | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0122 others(1): Show |
4 | HG02630.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-101C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84965809 | |||||||
chr1:84966027 | T | C | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-319A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966027 | |||||||
chr1:84966141 | T | C | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-433A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966141 | |||||||
chr1:84966156 | G | A | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-448C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966156 | |||||||
chr1:84966286 | A | C | 1 | a0002c0002t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.78-578T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966286 | |||||||
chr1:84966716 | C | A | 4 | a0001c0001t0002g0192 a0001c0001t0002g0294 a0001c0001t0031g0246 others(1): Show |
4 | HG00642.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1008G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966716 | |||||||
chr1:84966818 | G | C | 1 | a0001c0001t0002g0294 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.78-1110C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966818 | |||||||
chr1:84966822 | A | G | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-1114T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966822 | |||||||
chr1:84966829 | A | G | 1 | a0001c0001t0007g0117 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.78-1121T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966829 | |||||||
chr1:84966834 | A | C | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-1126T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966834 | |||||||
chr1:84966840 | T | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-1132A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966840 | |||||||
chr1:84966974 | C | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-1266G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84966974 | |||||||
chr1:84967120 | T | C | 1 | a0001c0001t0009g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.78-1412A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967120 | |||||||
chr1:84967152 | C | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(1): Show |
4 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1444G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967152 | |||||||
chr1:84967262 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.78-1554G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967262 | |||||||
chr1:84967264 | A | C | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-1556T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967264 | |||||||
chr1:84967580 | A | G | 8 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-1872T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967580 | |||||||
chr1:84967604 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-1896A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967604 | |||||||
chr1:84967740 | GGAGGGAG others(22): Show |
G | 21 | a0001c0001t0002g0292 a0001c0001t0002g0298 a0001c0001t0002g0299 others(18): Show |
22 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.78-2061_78-2033del others(29): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967740 | |||||||
chr1:84967748 | G | A | 1 | a0001c0001t0006g0297 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-2040C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967748 | |||||||
chr1:84967763 | AAGG | A | 97 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(94): Show |
101 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.78-2058_78-2056del others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967763 | |||||||
chr1:84967782 | G | A | 1 | a0001c0001t0006g0297 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-2074C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967782 | |||||||
chr1:84967783 | A | G | 1 | a0001c0001t0006g0297 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.78-2075T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84967783 | |||||||
chr1:84968393 | G | C | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-2685C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968393 | |||||||
chr1:84968417 | T | C | 1 | a0001c0001t0009g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.78-2709A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968417 | |||||||
chr1:84968423 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78-2715T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968423 | |||||||
chr1:84968853 | C | T | 92 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(89): Show |
96 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.78-3145G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968853 | |||||||
chr1:84968930 | T | C | 195 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(192): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-3222A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84968930 | |||||||
chr1:84969099 | G | A | 11 | a0001c0001t0002g0242 a0001c0001t0002g0247 a0001c0001t0003g0008 others(8): Show |
14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.78-3391C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969099 | |||||||
chr1:84969156 | G | A | 2 | a0001c0001t0014g0017 a0001c0001t0014g0022 |
2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.78-3448C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969156 | |||||||
chr1:84969326 | T | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-3618A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969326 | |||||||
chr1:84969362 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-3654C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969362 | |||||||
chr1:84969487 | T | C | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-3779A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969487 | |||||||
chr1:84969570 | C | CA | 10 | a0001c0001t0001g0077 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG00735.hp1 HG01433.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-3863dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969570 | |||||||
chr1:84969570 | CA | C | 79 | a0001c0001t0002g0192 a0001c0001t0002g0231 a0001c0001t0002g0237 others(76): Show |
84 | HG00140.hp1 HG00597.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.78-3863delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969570 | |||||||
chr1:84969712 | T | TA | 78 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(75): Show |
79 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.78-4005dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969712 | |||||||
chr1:84969716 | C | T | 3 | a0001c0001t0004g0129 a0001c0001t0004g0130 a0001c0001t0015g0127 |
3 | HG01081.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.78-4008G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969716 | |||||||
chr1:84969717 | C | T | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-4009G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969717 | |||||||
chr1:84969869 | C | T | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-4161G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969869 | |||||||
chr1:84969877 | G | A | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-4169C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969877 | |||||||
chr1:84969920 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0007g0119 a0001c0001t0020g0090 |
3 | HG01993.hp2 NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.78-4212T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969920 | |||||||
chr1:84969949 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-4241C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969949 | |||||||
chr1:84969995 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-4287C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84969995 | |||||||
chr1:84970031 | A | T | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-4323T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970031 | |||||||
chr1:84970043 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-4335T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970043 | |||||||
chr1:84970069 | G | T | 124 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(121): Show |
129 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.78-4361C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970069 | |||||||
chr1:84970204 | G | T | 1 | a0001c0001t0002g0280 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.78-4496C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970204 | |||||||
chr1:84970284 | C | T | 1 | a0001c0001t0004g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.78-4576G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970284 | |||||||
chr1:84970292 | C | T | 89 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(86): Show |
93 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.78-4584G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970292 | |||||||
chr1:84970376 | T | G | 1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-4668A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970376 | |||||||
chr1:84970435 | T | C | 128 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(125): Show |
133 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.78-4727A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970435 | |||||||
chr1:84970436 | G | A | 1 | a0001c0001t0014g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78-4728C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970436 | |||||||
chr1:84970445 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-4737C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970445 | |||||||
chr1:84970515 | CA | C | 10 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0002g0309 others(7): Show |
10 | HG00558.hp1 HG01928.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-4808delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970515 | |||||||
chr1:84970524 | A | T | 2 | a0001c0001t0001g0120 a0001c0001t0007g0119 |
2 | NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.78-4816T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970524 | |||||||
chr1:84970528 | A | T | 4 | a0001c0001t0001g0120 a0001c0001t0003g0194 a0001c0001t0007g0119 others(1): Show |
4 | HG01993.hp2 HG02135.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-4820T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970528 | |||||||
chr1:84970532 | T | A | 1 | a0001c0001t0003g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.78-4824A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970532 | |||||||
chr1:84970613 | G | T | 1 | a0001c0001t0002g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-4905C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970613 | |||||||
chr1:84970698 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.78-4990A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970698 | |||||||
chr1:84970707 | G | C | 1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78-4999C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970707 | |||||||
chr1:84970715 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.78-5007A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970715 | |||||||
chr1:84970779 | A | T | 195 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(192): Show |
205 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.78-5071T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970779 | |||||||
chr1:84970945 | G | A | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5237C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84970945 | |||||||
chr1:84971060 | T | C | 1 | a0001c0001t0003g0252 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.78-5352A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971060 | |||||||
chr1:84971243 | G | A | 128 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(125): Show |
133 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.78-5535C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971243 | |||||||
chr1:84971254 | T | C | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-5546A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971254 | |||||||
chr1:84971282 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.78-5574A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971282 | |||||||
chr1:84971434 | C | G | 9 | a0002c0002t0001g0124 a0004c0004t0001g0041 a0004c0004t0001g0042 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-5726G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971434 | |||||||
chr1:84971499 | T | TAC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
60 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.78-5793_78-5792dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | T | TACAC | 5 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0007g0053 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-5795_78-5792dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TAC | T | 66 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0067 others(63): Show |
68 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.78-5793_78-5792del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TACAC | T | 56 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0080 others(53): Show |
56 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.78-5795_78-5792del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TACACAC | T | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(63): Show |
70 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-5797_78-5792del others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TACACACA others(1): Show |
T | 15 | a0001c0001t0001g0086 a0001c0001t0001g0175 a0001c0001t0001g0177 others(12): Show |
15 | HG00673.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.78-5799_78-5792del others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TACACACA others(3): Show |
T | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.78-5801_78-5792del others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TACACACA others(5): Show |
T | 5 | a0003c0003t0005g0002 a0003c0003t0005g0030 a0003c0003t0005g0031 others(2): Show |
6 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.78-5803_78-5792del others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971499 | TACACACA others(9): Show |
T | 9 | a0002c0002t0001g0124 a0004c0004t0001g0041 a0004c0004t0001g0042 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-5807_78-5792del others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971499 | |||||||
chr1:84971591 | CAAAGT | C | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5888_78-5884del others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971591 | |||||||
chr1:84971605 | A | G | 1 | a0001c0001t0007g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78-5897T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971605 | |||||||
chr1:84971690 | T | C | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5982A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971690 | |||||||
chr1:84971803 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0003g0264 a0001c0001t0003g0265 |
3 | NA18980.hp2 NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78-6095G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971803 | |||||||
chr1:84971804 | G | A | 4 | a0001c0001t0002g0192 a0001c0001t0002g0294 a0001c0001t0031g0246 others(1): Show |
4 | HG00642.hp2 HG03130.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-6096C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84971804 | |||||||
chr1:84972169 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-6461A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972169 | |||||||
chr1:84972204 | C | A | 1 | a0001c0001t0002g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-6496G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972204 | |||||||
chr1:84972349 | T | C | 1 | a0001c0001t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78-6641A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972349 | |||||||
chr1:84972505 | T | G | 2 | a0001c0001t0004g0131 a0001c0001t0030g0089 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.78-6797A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972505 | |||||||
chr1:84972560 | C | A | 119 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(116): Show |
124 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.78-6852G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972560 | |||||||
chr1:84972636 | G | A | 1 | a0001c0001t0010g0333 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.78-6928C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972636 | |||||||
chr1:84972726 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-7018A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972726 | |||||||
chr1:84972935 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.78-7227A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84972935 | |||||||
chr1:84973174 | C | T | 3 | a0001c0001t0009g0050 a0001c0001t0009g0051 a0001c0001t0009g0052 |
3 | NA18747.hp1 NA18979.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.78-7466G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973174 | |||||||
chr1:84973376 | G | A | 188 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(185): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.78-7668C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973376 | |||||||
chr1:84973464 | G | A | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-7756C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973464 | |||||||
chr1:84973545 | A | G | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(20): Show |
24 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-7837T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973545 | |||||||
chr1:84973548 | T | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-7840A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973548 | |||||||
chr1:84973585 | C | T | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-7877G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973585 | |||||||
chr1:84973621 | T | G | 194 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(191): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.78-7913A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973621 | |||||||
chr1:84973687 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0080 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-7979C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973687 | |||||||
chr1:84973771 | T | C | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-8063A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973771 | |||||||
chr1:84973986 | T | A | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-8278A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84973986 | |||||||
chr1:84974021 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.78-8313G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974021 | |||||||
chr1:84974217 | C | T | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-8509G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974217 | |||||||
chr1:84974313 | C | A | 71 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(68): Show |
76 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.78-8605G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974313 | |||||||
chr1:84974340 | C | T | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.78-8632G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974340 | |||||||
chr1:84974341 | C | G | 1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.78-8633G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974341 | |||||||
chr1:84974451 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0007g0117 |
2 | NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.78-8743G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974451 | |||||||
chr1:84974466 | A | C | 1 | a0001c0001t0006g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.78-8758T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974466 | |||||||
chr1:84974530 | C | T | 89 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(86): Show |
93 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.78-8822G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974530 | |||||||
chr1:84974579 | C | G | 1 | a0001c0001t0008g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.78-8871G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974579 | |||||||
chr1:84974633 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78-8925C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974633 | |||||||
chr1:84974665 | G | T | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-8957C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974665 | |||||||
chr1:84974698 | T | G | 1 | a0001c0001t0003g0321 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.78-8990A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974698 | |||||||
chr1:84974708 | G | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-9000C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974708 | |||||||
chr1:84974964 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-9256C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974964 | |||||||
chr1:84974965 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-9257T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84974965 | |||||||
chr1:84975017 | G | A | 1 | a0001c0001t0004g0130 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.78-9309C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975017 | |||||||
chr1:84975018 | A | G | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.78-9310T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975018 | |||||||
chr1:84975110 | G | A | 116 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(113): Show |
121 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.78-9402C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975110 | |||||||
chr1:84975110 | G | T | 70 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(67): Show |
75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-9402C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975110 | |||||||
chr1:84975144 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.78-9436A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975144 | |||||||
chr1:84975144 | T | G | 1 | a0001c0001t0003g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.78-9436A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975144 | |||||||
chr1:84975154 | C | T | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-9446G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975154 | |||||||
chr1:84975210 | G | A | 1 | a0001c0001t0002g0307 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78-9502C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975210 | |||||||
chr1:84975234 | C | G | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-9526G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975234 | |||||||
chr1:84975368 | C | T | 194 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(191): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.78-9660G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975368 | |||||||
chr1:84975521 | A | C | 1 | a0001c0001t0002g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.78-9813T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975521 | |||||||
chr1:84975565 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78-9857T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975565 | |||||||
chr1:84975848 | T | A | 1 | a0002c0002t0001g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.78-10140A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975848 | |||||||
chr1:84975948 | G | A | 3 | a0001c0001t0002g0306 a0001c0001t0002g0317 a0001c0001t0002g0318 |
3 | HG02145.hp2 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.78-10240C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84975948 | |||||||
chr1:84976019 | A | G | 89 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(86): Show |
93 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.78-10311T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976019 | |||||||
chr1:84976102 | C | T | 194 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(191): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.78-10394G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976102 | |||||||
chr1:84976246 | G | A | 194 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(191): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.78-10538C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976246 | |||||||
chr1:84976263 | G | T | 1 | a0001c0001t0006g0308 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.78-10555C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976263 | |||||||
chr1:84976293 | T | TA | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-10586dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976293 | |||||||
chr1:84976536 | G | A | 70 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(67): Show |
75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-10828C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976536 | |||||||
chr1:84976553 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.78-10845C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976553 | |||||||
chr1:84976564 | G | A | 116 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(113): Show |
121 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.78-10856C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976564 | |||||||
chr1:84976697 | T | C | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-10989A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976697 | |||||||
chr1:84976964 | T | G | 194 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(191): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.78-11256A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84976964 | |||||||
chr1:84977025 | A | G | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-11317T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977025 | |||||||
chr1:84977123 | A | G | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-11415T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977123 | |||||||
chr1:84977130 | A | AT | 116 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(113): Show |
121 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.78-11423dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977130 | |||||||
chr1:84977130 | A | T | 70 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(67): Show |
75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-11422T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977130 | |||||||
chr1:84977188 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-11480A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977188 | |||||||
chr1:84977363 | T | TAAC | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-11656_78-11655i others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977363 | |||||||
chr1:84977440 | T | C | 4 | a0001c0001t0002g0247 a0002c0002t0002g0010 a0002c0002t0002g0236 others(1): Show |
5 | HG00639.hp2 HG01167.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-11732A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977440 | |||||||
chr1:84977458 | GA | G | 119 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0002g0192 others(116): Show |
124 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.78-11751delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977458 | |||||||
chr1:84977575 | G | A | 17 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0023 others(14): Show |
17 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.78-11867C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977575 | |||||||
chr1:84977656 | T | C | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0071 others(7): Show |
10 | HG01099.hp1 HG01109.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-11948A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977656 | |||||||
chr1:84977737 | G | T | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-12029C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977737 | |||||||
chr1:84977817 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78-12109C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977817 | |||||||
chr1:84977836 | T | G | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-12128A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977836 | |||||||
chr1:84977849 | C | T | 9 | a0001c0001t0002g0250 a0001c0001t0002g0253 a0001c0001t0002g0254 others(6): Show |
10 | HG02071.hp1 HG02080.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-12141G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977849 | |||||||
chr1:84977850 | A | G | 70 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(67): Show |
75 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.78-12142T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977850 | |||||||
chr1:84977922 | A | G | 120 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(117): Show |
125 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.78-12214T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84977922 | |||||||
chr1:84978124 | C | T | 1 | a0001c0001t0017g0159 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.78-12416G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978124 | |||||||
chr1:84978147 | G | T | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-12439C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978147 | |||||||
chr1:84978276 | CA | C | 177 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(174): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.78-12569delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978276 | |||||||
chr1:84978334 | AAAGC | A | 4 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-12630_78-12627d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978334 | |||||||
chr1:84978404 | T | A | 1 | a0003c0003t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.78-12696A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978404 | |||||||
chr1:84978414 | AAAAT | A | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-12710_78-12707d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978414 | |||||||
chr1:84978542 | C | T | 1 | a0001c0001t0013g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.78-12834G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978542 | |||||||
chr1:84978543 | T | G | 69 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(66): Show |
74 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.78-12835A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978543 | |||||||
chr1:84978562 | A | C | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-12854T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978562 | |||||||
chr1:84978714 | A | T | 1 | a0001c0001t0032g0278 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.78-13006T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978714 | |||||||
chr1:84978718 | T | A | 186 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(183): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.78-13010A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978718 | |||||||
chr1:84978757 | G | C | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-13049C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978757 | |||||||
chr1:84978799 | A | T | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-13091T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978799 | |||||||
chr1:84978811 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78-13103G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978811 | |||||||
chr1:84978823 | T | C | 7 | a0001c0001t0004g0082 a0001c0001t0004g0131 a0001c0001t0030g0089 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-13115A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978823 | |||||||
chr1:84978926 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0022g0144 |
2 | NA18990.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.78-13218G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84978926 | |||||||
chr1:84979030 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13322G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979030 | |||||||
chr1:84979063 | C | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13355G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979063 | |||||||
chr1:84979246 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13538A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979246 | |||||||
chr1:84979348 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-13640A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979348 | |||||||
chr1:84979454 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0003g0264 a0001c0001t0003g0265 |
3 | NA18980.hp2 NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78-13746G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979454 | |||||||
chr1:84979682 | A | G | 7 | a0001c0001t0002g0250 a0001c0001t0002g0270 a0001c0001t0002g0271 others(4): Show |
8 | HG02071.hp1 HG02080.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-13974T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979682 | |||||||
chr1:84979701 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
153 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.78-13993A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979701 | |||||||
chr1:84979717 | C | A | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.78-14009G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979717 | |||||||
chr1:84979946 | A | C | 1 | a0001c0001t0004g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.78-14238T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84979946 | |||||||
chr1:84980001 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.78-14293G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980001 | |||||||
chr1:84980063 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.78-14355G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980063 | |||||||
chr1:84980136 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.78-14428C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980136 | |||||||
chr1:84980143 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.78-14435C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980143 | |||||||
chr1:84980305 | G | GA | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.78-14598dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980305 | |||||||
chr1:84980393 | A | C | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.78-14685T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980393 | |||||||
chr1:84980439 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.78-14731G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980439 | |||||||
chr1:84980580 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.78-14872C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980580 | |||||||
chr1:84980803 | G | A | 1 | a0003c0003t0005g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.78-15095C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84980803 | |||||||
chr1:84981004 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.78-15296C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981004 | |||||||
chr1:84981097 | CAAT | C | 9 | a0001c0001t0001g0057 a0001c0001t0001g0071 a0001c0001t0001g0077 others(6): Show |
9 | HG01099.hp1 HG01109.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.78-15392_78-15390d others(5): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981097 | |||||||
chr1:84981651 | G | A | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+15145C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981651 | |||||||
chr1:84981737 | G | A | 3 | a0001c0001t0002g0294 a0001c0001t0031g0246 a0007c0010t0002g0245 |
3 | HG00642.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.77+15059C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981737 | |||||||
chr1:84981740 | C | T | 1 | a0001c0001t0003g0296 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.77+15056G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981740 | |||||||
chr1:84981910 | A | G | 43 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(40): Show |
43 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.77+14886T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981910 | |||||||
chr1:84981951 | CA | C | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+14844delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981951 | |||||||
chr1:84981976 | A | T | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+14820T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981976 | |||||||
chr1:84981980 | A | C | 166 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(163): Show |
175 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.77+14816T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84981980 | |||||||
chr1:84982074 | G | GT | 155 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(152): Show |
164 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.77+14721dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982074 | |||||||
chr1:84982074 | G | GTT | 7 | a0001c0001t0002g0307 a0001c0001t0012g0259 a0004c0004t0001g0046 others(4): Show |
7 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+14720_77+14721d others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982074 | |||||||
chr1:84982086 | T | A | 1 | a0003c0003t0005g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.77+14710A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982086 | |||||||
chr1:84982087 | T | A | 5 | a0003c0003t0005g0002 a0003c0003t0005g0030 a0003c0003t0005g0031 others(2): Show |
6 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+14709A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982087 | |||||||
chr1:84982088 | A | T | 172 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0122 others(169): Show |
181 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.77+14708T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982088 | |||||||
chr1:84982089 | A | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0191 a0001c0001t0002g0192 others(73): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+14707T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982089 | |||||||
chr1:84982090 | A | T | 13 | a0001c0001t0002g0253 a0001c0001t0003g0190 a0001c0001t0003g0282 others(10): Show |
13 | HG00323.hp2 HG00558.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.77+14706T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982090 | |||||||
chr1:84982146 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+14650A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982146 | |||||||
chr1:84982156 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.77+14640T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982156 | |||||||
chr1:84982220 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0025g0088 |
2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+14576C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982220 | |||||||
chr1:84982225 | A | G | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+14571T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982225 | |||||||
chr1:84982382 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0007g0110 |
3 | HG01243.hp1 HG02148.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.77+14414G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982382 | |||||||
chr1:84982383 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.77+14413C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982383 | |||||||
chr1:84982445 | T | A | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+14351A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982445 | |||||||
chr1:84982454 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.77+14342T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982454 | |||||||
chr1:84982579 | G | A | 4 | a0001c0001t0002g0222 a0001c0001t0002g0224 a0001c0001t0011g0223 others(1): Show |
4 | HG03654.hp1 HG03710.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+14217C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982579 | |||||||
chr1:84982666 | T | C | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+14130A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982666 | |||||||
chr1:84982668 | A | G | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+14128T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982668 | |||||||
chr1:84982768 | T | A | 7 | a0001c0001t0002g0307 a0001c0001t0002g0309 a0001c0001t0002g0320 others(4): Show |
7 | HG04228.hp1 NA18951.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+14028A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982768 | |||||||
chr1:84982778 | C | T | 1 | a0001c0001t0005g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.77+14018G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982778 | |||||||
chr1:84982901 | A | G | 2 | a0001c0001t0003g0183 a0001c0001t0006g0184 |
2 | NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+13895T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982901 | |||||||
chr1:84982917 | T | A | 2 | a0001c0001t0002g0250 a0001c0001t0008g0272 |
2 | HG02071.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.77+13879A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982917 | |||||||
chr1:84982983 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.77+13813C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84982983 | |||||||
chr1:84983013 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+13783G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983013 | |||||||
chr1:84983129 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0029 a0001c0001t0005g0034 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+13667C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983129 | |||||||
chr1:84983228 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0122 others(1): Show |
4 | HG02630.hp2 HG02897.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+13568G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983228 | |||||||
chr1:84983264 | TTTTTC | T | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+13527_77+13531d others(7): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983264 | |||||||
chr1:84983371 | G | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+13425C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983371 | |||||||
chr1:84983397 | T | C | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+13399A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983397 | |||||||
chr1:84983422 | C | T | 28 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(25): Show |
29 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.77+13374G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983422 | |||||||
chr1:84983536 | A | G | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+13260T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983536 | |||||||
chr1:84983568 | T | C | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+13228A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983568 | |||||||
chr1:84983676 | C | CT | 21 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0071 others(18): Show |
21 | HG01099.hp1 HG01109.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+13119dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983676 | |||||||
chr1:84983676 | CT | C | 76 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(73): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+13119delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983676 | |||||||
chr1:84983802 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+12994C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983802 | |||||||
chr1:84983822 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0004g0083 a0001c0001t0004g0105 others(2): Show |
5 | HG00408.hp1 HG00621.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+12974C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983822 | |||||||
chr1:84983882 | G | A | 3 | a0001c0001t0004g0129 a0001c0001t0004g0130 a0001c0001t0015g0127 |
3 | HG01081.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.77+12914C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983882 | |||||||
chr1:84983925 | C | T | 1 | a0001c0001t0009g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.77+12871G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983925 | |||||||
chr1:84983966 | G | C | 168 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(165): Show |
177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+12830C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84983966 | |||||||
chr1:84984014 | T | C | 168 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(165): Show |
177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+12782A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984014 | |||||||
chr1:84984040 | T | C | 1 | a0001c0001t0018g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.77+12756A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984040 | |||||||
chr1:84984370 | C | G | 4 | a0001c0001t0001g0155 a0001c0001t0001g0174 a0001c0001t0004g0156 others(1): Show |
4 | HG00408.hp2 HG00621.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+12426G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984370 | |||||||
chr1:84984386 | G | T | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+12410C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984386 | |||||||
chr1:84984396 | C | CT | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+12399dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984396 | |||||||
chr1:84984637 | G | A | 167 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(164): Show |
176 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.77+12159C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984637 | |||||||
chr1:84984681 | A | G | 1 | a0001c0001t0002g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.77+12115T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984681 | |||||||
chr1:84984705 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.77+12091T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984705 | |||||||
chr1:84984725 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0274 |
3 | HG00280.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.77+12071C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984725 | |||||||
chr1:84984789 | G | A | 68 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(65): Show |
73 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.77+12007C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984789 | |||||||
chr1:84984924 | A | T | 1 | a0001c0001t0002g0258 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.77+11872T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984924 | |||||||
chr1:84984944 | T | C | 161 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(158): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+11852A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984944 | |||||||
chr1:84984983 | G | C | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+11813C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84984983 | |||||||
chr1:84985043 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.77+11753G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985043 | |||||||
chr1:84985237 | T | C | 164 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(161): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.77+11559A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985237 | |||||||
chr1:84985404 | C | T | 164 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(161): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.77+11392G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985404 | |||||||
chr1:84985460 | G | A | 164 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(161): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.77+11336C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985460 | |||||||
chr1:84985522 | A | G | 1 | a0001c0001t0003g0316 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.77+11274T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985522 | |||||||
chr1:84985571 | G | T | 1 | a0004c0004t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+11225C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985571 | |||||||
chr1:84985702 | A | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+11094T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985702 | |||||||
chr1:84985745 | A | G | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.77+11051T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985745 | |||||||
chr1:84985942 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.77+10854A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84985942 | |||||||
chr1:84986082 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+10714A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986082 | |||||||
chr1:84986159 | C | T | 1 | a0001c0001t0002g0328 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.77+10637G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986159 | |||||||
chr1:84986162 | C | T | 3 | a0001c0001t0001g0134 a0005c0006t0001g0132 a0005c0006t0024g0133 |
3 | HG01099.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.77+10634G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986162 | |||||||
chr1:84986163 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.77+10633C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986163 | |||||||
chr1:84986241 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.77+10555A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986241 | |||||||
chr1:84986262 | C | T | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+10534G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986262 | |||||||
chr1:84986339 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.77+10457T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986339 | |||||||
chr1:84986404 | G | C | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+10392C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986404 | |||||||
chr1:84986474 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.77+10322G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986474 | |||||||
chr1:84986475 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+10321C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986475 | |||||||
chr1:84986543 | C | CA | 78 | a0001c0001t0001g0173 a0001c0001t0002g0015 a0001c0001t0002g0189 others(75): Show |
83 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.77+10252dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986543 | |||||||
chr1:84986543 | CA | C | 8 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(5): Show |
8 | HG02055.hp2 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+10252delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986543 | |||||||
chr1:84986592 | G | GAATA | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+10200_77+10203d others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986592 | |||||||
chr1:84986595 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.77+10201A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986595 | |||||||
chr1:84986639 | T | TGACAAAG others(65): Show |
1 | a0001c0001t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.77+10085_77+10156d others(74): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986639 | |||||||
chr1:84986711 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.77+10085C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986711 | |||||||
chr1:84986769 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.77+10027G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986769 | |||||||
chr1:84986897 | G | A | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9899C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986897 | |||||||
chr1:84986967 | A | T | 1 | a0003c0003t0013g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.77+9829T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84986967 | |||||||
chr1:84987025 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0313 |
3 | NA18983.hp2 NA19000.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.77+9771C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987025 | |||||||
chr1:84987054 | T | C | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9742A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987054 | |||||||
chr1:84987176 | A | ATATC | 5 | a0001c0001t0001g0100 a0001c0001t0002g0237 a0001c0001t0003g0182 others(2): Show |
5 | HG01433.hp2 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9616_77+9619dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987176 | |||||||
chr1:84987176 | ATATC | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.77+9616_77+9619del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987176 | |||||||
chr1:84987176 | ATATCTAT others(1): Show |
A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0007g0058 |
3 | HG01099.hp1 HG02683.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.77+9612_77+9619del others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987176 | |||||||
chr1:84987184 | C | G | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9612G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987184 | |||||||
chr1:84987200 | CTATCTAT others(7): Show |
C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9582_77+9595del others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987200 | |||||||
chr1:84987206 | A | T | 11 | a0001c0001t0002g0242 a0001c0001t0002g0247 a0001c0001t0003g0008 others(8): Show |
14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+9590T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987206 | |||||||
chr1:84987208 | C | A | 7 | a0001c0001t0001g0141 a0001c0001t0001g0164 a0001c0001t0004g0150 others(4): Show |
8 | HG01928.hp1 HG01943.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9588G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987208 | |||||||
chr1:84987208 | CTATA | C | 62 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0198 others(59): Show |
65 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.77+9584_77+9587del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987208 | |||||||
chr1:84987212 | A | C | 28 | a0001c0001t0002g0237 a0001c0001t0002g0290 a0001c0001t0002g0292 others(25): Show |
29 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.77+9584T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987212 | |||||||
chr1:84987244 | T | G | 69 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(66): Show |
74 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.77+9552A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987244 | |||||||
chr1:84987245 | G | A | 1 | a0001c0001t0035g0319 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.77+9551C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987245 | |||||||
chr1:84987257 | A | G | 1 | a0002c0002t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+9539T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987257 | |||||||
chr1:84987267 | GTA | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.77+9527_77+9528del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987267 | |||||||
chr1:84987271 | A | ATATATC | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9524_77+9525ins others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987271 | |||||||
chr1:84987365 | T | G | 9 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+9431A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987365 | |||||||
chr1:84987374 | T | G | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9422A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987374 | |||||||
chr1:84987386 | A | G | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9410T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987386 | |||||||
chr1:84987411 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9385A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987411 | |||||||
chr1:84987413 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9383A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987413 | |||||||
chr1:84987424 | C | A | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9372G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987424 | |||||||
chr1:84987432 | G | GTATATAT others(65): Show |
7 | a0001c0001t0002g0250 a0001c0001t0002g0270 a0001c0001t0002g0271 others(4): Show |
8 | HG02071.hp1 HG02080.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9363_77+9364ins others(72): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987432 | |||||||
chr1:84987439 | G | C | 8 | a0001c0001t0002g0235 a0001c0001t0002g0250 a0001c0001t0002g0270 others(5): Show |
9 | HG02071.hp1 HG02080.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+9357C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987439 | |||||||
chr1:84987440 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.77+9356T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987440 | |||||||
chr1:84987471 | G | C | 1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+9325C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987471 | |||||||
chr1:84987471 | G | T | 45 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(42): Show |
46 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.77+9325C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987471 | |||||||
chr1:84987472 | A | C | 1 | a0001c0001t0008g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.77+9324T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987472 | |||||||
chr1:84987473 | T | C | 45 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(42): Show |
46 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.77+9323A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987473 | |||||||
chr1:84987474 | A | ATATACAT others(193): Show |
1 | a0001c0001t0002g0235 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.77+9321_77+9322ins others(200): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987474 | |||||||
chr1:84987488 | A | G | 5 | a0001c0001t0002g0235 a0004c0004t0001g0046 a0006c0005t0001g0044 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9308T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987488 | |||||||
chr1:84987489 | C | CAT | 16 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0080 others(13): Show |
16 | HG00609.hp2 HG00642.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+9305_77+9306dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATA others(161): Show |
13 | a0001c0001t0002g0255 a0001c0001t0002g0281 a0001c0001t0002g0289 others(10): Show |
16 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(168): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATA others(405): Show |
1 | a0004c0004t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(412): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATA others(381): Show |
1 | a0009c0007t0004g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(388): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATA others(333): Show |
1 | a0004c0004t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(340): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATA others(123): Show |
1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(130): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATG others(157): Show |
1 | a0001c0001t0002g0286 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(164): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATG others(195): Show |
31 | a0001c0001t0002g0189 a0001c0001t0002g0193 a0001c0001t0002g0258 others(28): Show |
31 | HG00323.hp2 HG00558.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(202): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATG others(213): Show |
1 | a0001c0001t0006g0284 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(220): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATG others(275): Show |
1 | a0001c0001t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(282): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATG others(229): Show |
2 | a0001c0001t0002g0015 a0001c0001t0002g0274 |
3 | HG00280.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(236): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATATG others(187): Show |
1 | a0001c0001t0002g0324 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.77+9306_77+9307ins others(194): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | CATATGTA others(37): Show |
20 | a0001c0001t0005g0019 a0001c0001t0005g0023 a0001c0001t0005g0026 others(17): Show |
21 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.77+9306_77+9307ins others(44): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987489 | C | T | 5 | a0001c0001t0002g0235 a0004c0004t0001g0046 a0006c0005t0001g0044 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9307G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987489 | |||||||
chr1:84987490 | A | ATATGTAT others(49): Show |
4 | a0001c0001t0002g0228 a0001c0001t0002g0318 a0001c0001t0006g0234 others(1): Show |
4 | HG02145.hp2 HG02155.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9305_77+9306ins others(56): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987490 | |||||||
chr1:84987490 | A | ATATGTAT others(73): Show |
1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.77+9305_77+9306ins others(80): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987490 | |||||||
chr1:84987494 | G | A | 64 | a0001c0001t0001g0061 a0001c0001t0002g0015 a0001c0001t0002g0189 others(61): Show |
69 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.77+9302C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987494 | |||||||
chr1:84987494 | G | GTGTATAC others(3): Show |
1 | a0001c0001t0003g0209 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.77+9301_77+9302ins others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987494 | |||||||
chr1:84987495 | T | TACATATA others(49): Show |
1 | a0004c0004t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9300_77+9301ins others(56): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | |||||||
chr1:84987495 | T | TAGATATA others(75): Show |
4 | a0004c0004t0001g0046 a0006c0005t0001g0044 a0006c0005t0001g0045 others(1): Show |
4 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9300_77+9301ins others(82): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | |||||||
chr1:84987495 | T | TATATACC others(7): Show |
134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.77+9300_77+9301ins others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | |||||||
chr1:84987495 | T | TATATATC others(7): Show |
1 | a0001c0001t0007g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.77+9300_77+9301ins others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | |||||||
chr1:84987495 | T | TGTATATA others(9): Show |
8 | a0001c0001t0001g0061 a0001c0001t0002g0250 a0001c0001t0002g0270 others(5): Show |
9 | HG01346.hp1 HG02071.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+9300_77+9301ins others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987495 | |||||||
chr1:84987496 | A | ATATACCT others(7): Show |
57 | a0001c0001t0001g0152 a0001c0001t0002g0197 a0001c0001t0002g0198 others(54): Show |
59 | HG00609.hp1 HG00639.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.77+9299_77+9300ins others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987496 | |||||||
chr1:84987497 | TAC | T | 28 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(25): Show |
28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9297_77+9298del others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987497 | |||||||
chr1:84987499 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.77+9297G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987499 | |||||||
chr1:84987500 | A | C | 1 | a0003c0003t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9296T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987500 | |||||||
chr1:84987503 | G | C | 28 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(25): Show |
28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9293C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987503 | |||||||
chr1:84987503 | G | T | 52 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(49): Show |
56 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+9293C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987503 | |||||||
chr1:84987504 | A | ATATATAT others(177): Show |
1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+9291_77+9292ins others(184): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | |||||||
chr1:84987504 | A | ATATATAT others(39): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG01109.hp2 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9291_77+9292ins others(46): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | |||||||
chr1:84987504 | A | C | 28 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(25): Show |
28 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9292T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | |||||||
chr1:84987504 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.77+9292T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987504 | |||||||
chr1:84987506 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.77+9290C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987506 | |||||||
chr1:84987507 | T | C | 1 | a0003c0003t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9289A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987507 | |||||||
chr1:84987509 | T | TATACATA others(297): Show |
1 | a0001c0001t0002g0268 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77+9286_77+9287ins others(304): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987509 | |||||||
chr1:84987511 | C | T | 62 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(59): Show |
66 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.77+9285G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987511 | |||||||
chr1:84987511 | CATAT | C | 18 | a0001c0001t0002g0292 a0001c0001t0002g0298 a0001c0001t0002g0299 others(15): Show |
18 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.77+9281_77+9284del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987511 | |||||||
chr1:84987512 | A | ACATATAT others(253): Show |
1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.77+9283_77+9284ins others(260): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987512 | |||||||
chr1:84987512 | A | ATC | 5 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0318 others(2): Show |
5 | HG00673.hp1 HG02145.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9283_77+9284ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987512 | |||||||
chr1:84987512 | ATATG | A | 9 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+9280_77+9283del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987512 | |||||||
chr1:84987513 | T | C | 8 | a0001c0001t0002g0248 a0001c0001t0002g0253 a0001c0001t0002g0254 others(5): Show |
8 | HG00609.hp2 HG00642.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9283A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987513 | |||||||
chr1:84987515 | T | G | 1 | a0003c0003t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9281A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987515 | |||||||
chr1:84987515 | TGTATATA others(43): Show |
T | 1 | a0008c0012t0005g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9231_77+9280del others(50): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987515 | |||||||
chr1:84987516 | G | A | 63 | a0001c0001t0001g0077 a0001c0001t0002g0015 a0001c0001t0002g0189 others(60): Show |
67 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.77+9280C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987516 | |||||||
chr1:84987517 | T | C | 27 | a0001c0001t0002g0189 a0001c0001t0002g0193 a0001c0001t0002g0255 others(24): Show |
30 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.77+9279A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987517 | |||||||
chr1:84987517 | T | TAC | 25 | a0001c0001t0001g0077 a0001c0001t0002g0015 a0001c0001t0002g0235 others(22): Show |
26 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.77+9278_77+9279ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987517 | |||||||
chr1:84987517 | T | TATAC | 5 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0318 others(2): Show |
5 | HG00673.hp1 HG02145.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9278_77+9279ins others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987517 | |||||||
chr1:84987518 | A | G | 2 | a0004c0004t0001g0042 a0009c0007t0004g0043 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77+9278T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987518 | |||||||
chr1:84987521 | T | C | 8 | a0001c0001t0002g0248 a0001c0001t0002g0253 a0001c0001t0002g0254 others(5): Show |
8 | HG00609.hp2 HG00642.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9275A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987521 | |||||||
chr1:84987521 | T | G | 6 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0318 others(3): Show |
6 | HG00673.hp1 HG02145.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+9275A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987521 | |||||||
chr1:84987521 | T | TATGTATA others(17): Show |
58 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0001g0080 others(55): Show |
58 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.77+9251_77+9274dup others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987521 | |||||||
chr1:84987523 | T | C | 1 | a0003c0003t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9273A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987523 | |||||||
chr1:84987523 | T | G | 27 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(24): Show |
27 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.77+9273A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987523 | |||||||
chr1:84987524 | G | A | 15 | a0001c0001t0002g0191 a0001c0001t0002g0248 a0001c0001t0002g0253 others(12): Show |
15 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+9272C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987524 | |||||||
chr1:84987526 | ATACATCT others(3): Show |
A | 2 | a0001c0001t0005g0021 a0001c0001t0005g0025 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.77+9260_77+9269del others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987526 | |||||||
chr1:84987528 | A | G | 1 | a0003c0003t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+9268T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987528 | |||||||
chr1:84987529 | C | T | 89 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(86): Show |
94 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.77+9267G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987529 | |||||||
chr1:84987531 | T | C | 25 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(22): Show |
25 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+9265A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987531 | |||||||
chr1:84987531 | T | G | 11 | a0001c0001t0002g0250 a0001c0001t0002g0270 a0001c0001t0002g0271 others(8): Show |
12 | HG02071.hp1 HG02080.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+9265A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987531 | |||||||
chr1:84987532 | C | A | 53 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(50): Show |
54 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.77+9264G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987532 | |||||||
chr1:84987533 | T | G | 51 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(48): Show |
55 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.77+9263A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987533 | |||||||
chr1:84987533 | T | TATGTATA others(17): Show |
1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.77+9262_77+9263ins others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987533 | |||||||
chr1:84987536 | G | A | 63 | a0001c0001t0001g0077 a0001c0001t0002g0015 a0001c0001t0002g0189 others(60): Show |
68 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.77+9260C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987536 | |||||||
chr1:84987536 | GTATACAT others(41): Show |
G | 5 | a0001c0001t0001g0122 a0001c0001t0002g0204 a0001c0001t0002g0230 others(2): Show |
5 | HG00642.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+9212_77+9259del others(48): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987536 | |||||||
chr1:84987537 | T | C | 11 | a0001c0001t0002g0250 a0001c0001t0002g0270 a0001c0001t0002g0271 others(8): Show |
12 | HG02071.hp1 HG02080.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+9259A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987537 | |||||||
chr1:84987537 | TATAC | T | 21 | a0001c0001t0002g0292 a0001c0001t0002g0298 a0001c0001t0002g0299 others(18): Show |
21 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+9255_77+9258del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987537 | |||||||
chr1:84987537 | TATACATA others(33): Show |
T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0070 others(1): Show |
4 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9219_77+9258del others(40): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987537 | |||||||
chr1:84987540 | A | C | 1 | a0004c0004t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9256T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987540 | |||||||
chr1:84987541 | C | CATATATA others(43): Show |
1 | a0001c0001t0001g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.77+9254_77+9255ins others(50): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987541 | |||||||
chr1:84987541 | C | T | 15 | a0001c0001t0002g0191 a0001c0001t0002g0248 a0001c0001t0002g0253 others(12): Show |
15 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+9255G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987541 | |||||||
chr1:84987544 | A | C | 1 | a0001c0001t0002g0268 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.77+9252T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987544 | |||||||
chr1:84987545 | G | GATATATA others(3): Show |
2 | a0001c0001t0031g0246 a0007c0010t0002g0245 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+9250_77+9251ins others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987545 | |||||||
chr1:84987545 | G | T | 73 | a0001c0001t0001g0077 a0001c0001t0002g0015 a0001c0001t0002g0189 others(70): Show |
77 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.77+9251C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987545 | |||||||
chr1:84987548 | G | A | 26 | a0001c0001t0002g0191 a0001c0001t0002g0248 a0001c0001t0002g0250 others(23): Show |
27 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.77+9248C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987548 | |||||||
chr1:84987552 | A | ATACATAT others(215): Show |
1 | a0001c0001t0002g0322 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.77+9243_77+9244ins others(222): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | |||||||
chr1:84987552 | A | ATACATAT others(263): Show |
1 | a0001c0001t0002g0248 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.77+9243_77+9244ins others(270): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | |||||||
chr1:84987552 | A | ATACATAT others(225): Show |
2 | a0001c0001t0003g0282 a0001c0001t0011g0269 |
2 | HG02135.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.77+9243_77+9244ins others(232): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | |||||||
chr1:84987552 | A | ATACATAT others(235): Show |
2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.77+9243_77+9244ins others(242): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | |||||||
chr1:84987552 | ACATC | A | 3 | a0001c0001t0003g0283 a0001c0001t0005g0021 a0001c0001t0005g0025 |
3 | HG01978.hp2 HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.77+9240_77+9243del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987552 | |||||||
chr1:84987553 | C | T | 56 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(53): Show |
60 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.77+9243G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987553 | |||||||
chr1:84987556 | C | A | 26 | a0001c0001t0002g0191 a0001c0001t0002g0248 a0001c0001t0002g0250 others(23): Show |
27 | HG00609.hp2 HG00642.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.77+9240G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987556 | |||||||
chr1:84987557 | T | G | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+9239A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987557 | |||||||
chr1:84987560 | G | A | 57 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(54): Show |
61 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.77+9236C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | |||||||
chr1:84987560 | G | GTATATAG others(3): Show |
3 | a0004c0004t0001g0042 a0004c0004t0001g0048 a0009c0007t0004g0043 |
3 | HG02109.hp2 HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.77+9235_77+9236ins others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | |||||||
chr1:84987560 | G | GTATATAT others(1): Show |
3 | a0001c0001t0002g0191 a0001c0001t0002g0268 a0001c0001t0003g0186 |
3 | HG01515.hp1 NA18975.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.77+9235_77+9236ins others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | |||||||
chr1:84987560 | G | GTATATAT others(173): Show |
1 | a0001c0001t0008g0273 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.77+9235_77+9236ins others(180): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | |||||||
chr1:84987560 | G | GTATATAT others(173): Show |
6 | a0001c0001t0002g0250 a0001c0001t0002g0270 a0001c0001t0002g0271 others(3): Show |
7 | HG02071.hp1 HG03669.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+9235_77+9236ins others(180): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | |||||||
chr1:84987560 | GTATACAT others(17): Show |
G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.77+9212_77+9235del others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987560 | |||||||
chr1:84987561 | T | TATCTATA others(147): Show |
1 | a0004c0004t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.77+9234_77+9235ins others(154): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987561 | |||||||
chr1:84987561 | T | TATCTATA others(147): Show |
1 | a0006c0005t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.77+9234_77+9235ins others(154): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987561 | |||||||
chr1:84987561 | T | TATCTATA others(147): Show |
2 | a0006c0005t0001g0045 a0006c0005t0001g0047 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.77+9234_77+9235ins others(154): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987561 | |||||||
chr1:84987564 | A | C | 1 | a0004c0004t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9232T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987564 | |||||||
chr1:84987565 | C | T | 1 | a0004c0004t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9231G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987565 | |||||||
chr1:84987566 | A | C | 2 | a0001c0001t0031g0246 a0007c0010t0002g0245 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+9230T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987566 | |||||||
chr1:84987569 | G | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(73): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+9227C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987569 | |||||||
chr1:84987570 | A | G | 1 | a0008c0012t0005g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9226T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987570 | |||||||
chr1:84987572 | G | A | 4 | a0001c0001t0031g0246 a0004c0004t0001g0041 a0007c0010t0002g0245 others(1): Show |
4 | HG00642.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9224C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987572 | |||||||
chr1:84987573 | T | C | 2 | a0001c0001t0031g0246 a0007c0010t0002g0245 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+9223A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987573 | |||||||
chr1:84987577 | C | CATCTATG others(13): Show |
1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+9218_77+9219ins others(20): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987577 | |||||||
chr1:84987577 | C | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(73): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+9219G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987577 | |||||||
chr1:84987580 | A | AGATATAT others(273): Show |
1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+9215_77+9216ins others(280): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | |||||||
chr1:84987580 | A | AGATATAT others(251): Show |
1 | a0001c0001t0031g0246 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.77+9215_77+9216ins others(258): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | |||||||
chr1:84987580 | A | ATATGTAT others(339): Show |
1 | a0004c0004t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.77+9215_77+9216ins others(346): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | |||||||
chr1:84987580 | A | C | 127 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0069 others(124): Show |
128 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.77+9216T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987580 | |||||||
chr1:84987581 | G | C | 1 | a0001c0001t0004g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+9215C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987581 | |||||||
chr1:84987581 | G | T | 106 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0057 others(103): Show |
106 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.77+9215C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987581 | |||||||
chr1:84987582 | A | G | 2 | a0001c0001t0005g0021 a0001c0001t0005g0025 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.77+9214T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987582 | |||||||
chr1:84987584 | A | G | 106 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0057 others(103): Show |
106 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.77+9212T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987584 | |||||||
chr1:84987585 | T | G | 4 | a0004c0004t0001g0046 a0006c0005t0001g0044 a0006c0005t0001g0045 others(1): Show |
4 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9211A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987585 | |||||||
chr1:84987589 | C | CAT | 30 | a0001c0001t0002g0191 a0001c0001t0002g0248 a0001c0001t0002g0250 others(27): Show |
31 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.77+9205_77+9206dup others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(61): Show |
3 | a0001c0001t0003g0011 a0001c0001t0003g0251 a0001c0001t0003g0252 |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(68): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(63): Show |
4 | a0001c0001t0002g0287 a0001c0001t0003g0190 a0001c0001t0006g0277 others(1): Show |
4 | HG00323.hp2 NA18612.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(70): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(33): Show |
2 | a0001c0001t0002g0323 a0001c0001t0002g0327 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(40): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(63): Show |
1 | a0001c0001t0002g0281 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.77+9206_77+9207ins others(70): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(61): Show |
2 | a0001c0001t0002g0274 a0001c0001t0013g0028 |
2 | HG00280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(68): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(57): Show |
4 | a0001c0001t0002g0324 a0001c0001t0002g0326 a0001c0001t0002g0328 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(64): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | CATATATG others(63): Show |
28 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0193 others(25): Show |
31 | HG00558.hp1 HG01255.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.77+9206_77+9207ins others(70): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987589 | C | T | 1 | a0008c0012t0005g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9207G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987589 | |||||||
chr1:84987592 | A | G | 1 | a0008c0012t0005g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9204T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987592 | |||||||
chr1:84987594 | G | A | 1 | a0008c0012t0005g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9202C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987594 | |||||||
chr1:84987597 | T | C | 1 | a0008c0012t0005g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.77+9199A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987597 | |||||||
chr1:84987613 | T | C | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+9183A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987613 | |||||||
chr1:84987619 | T | TATAC | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9173_77+9176dup others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987619 | |||||||
chr1:84987619 | T | TATACATA others(61): Show |
1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+9176_77+9177ins others(68): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987619 | |||||||
chr1:84987631 | T | C | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+9165A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987631 | |||||||
chr1:84987657 | C | CATATGTA others(23): Show |
5 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0003g0011 others(2): Show |
6 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+9138_77+9139ins others(30): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | |||||||
chr1:84987657 | C | CATATGTA others(103): Show |
7 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(4): Show |
7 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+9138_77+9139ins others(110): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | |||||||
chr1:84987657 | C | CATATGTA others(129): Show |
1 | a0009c0007t0004g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+9138_77+9139ins others(136): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | |||||||
chr1:84987657 | C | CGTATGTA others(41): Show |
1 | a0001c0001t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77+9138_77+9139ins others(48): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987657 | |||||||
chr1:84987659 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.77+9137A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | |||||||
chr1:84987659 | T | TATGTATA others(41): Show |
54 | a0001c0001t0002g0189 a0001c0001t0002g0193 a0001c0001t0002g0235 others(51): Show |
57 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+9136_77+9137ins others(48): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | |||||||
chr1:84987659 | T | TATGTATA others(67): Show |
6 | a0001c0001t0002g0274 a0001c0001t0006g0275 a0001c0001t0006g0276 others(3): Show |
6 | HG00280.hp2 HG02056.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+9136_77+9137ins others(74): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | |||||||
chr1:84987659 | T | TATGTATA others(93): Show |
1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+9136_77+9137ins others(100): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | |||||||
chr1:84987659 | T | TATGTATA others(119): Show |
1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+9136_77+9137ins others(126): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | |||||||
chr1:84987659 | T | TATGTATA others(101): Show |
1 | a0001c0001t0002g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.77+9136_77+9137ins others(108): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987659 | |||||||
chr1:84987669 | T | G | 13 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0003g0011 others(10): Show |
14 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+9127A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987669 | |||||||
chr1:84987670 | G | A | 13 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0003g0011 others(10): Show |
14 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+9126C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987670 | |||||||
chr1:84987670 | G | GTATATAG others(1): Show |
64 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(61): Show |
68 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.77+9118_77+9125dup others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987670 | |||||||
chr1:84987679 | T | A | 1 | a0001c0001t0002g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+9117A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987679 | |||||||
chr1:84987705 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9091A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987705 | |||||||
chr1:84987730 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+9066A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987730 | |||||||
chr1:84987788 | C | T | 87 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(84): Show |
91 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.77+9008G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987788 | |||||||
chr1:84987903 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.77+8893A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987903 | |||||||
chr1:84987978 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.77+8818A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987978 | |||||||
chr1:84987996 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8800A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84987996 | |||||||
chr1:84988132 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.77+8664C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988132 | |||||||
chr1:84988133 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.77+8663G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988133 | |||||||
chr1:84988182 | A | G | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+8614T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988182 | |||||||
chr1:84988210 | T | A | 1 | a0001c0001t0002g0242 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.77+8586A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988210 | |||||||
chr1:84988210 | TA | T | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8585delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988210 | |||||||
chr1:84988211 | A | T | 1 | a0001c0001t0001g0006 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.77+8585T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988211 | |||||||
chr1:84988313 | A | G | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+8483T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988313 | |||||||
chr1:84988418 | T | C | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+8378A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988418 | |||||||
chr1:84988426 | C | G | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8370G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988426 | |||||||
chr1:84988442 | G | A | 7 | a0001c0001t0002g0307 a0001c0001t0002g0309 a0001c0001t0002g0320 others(4): Show |
7 | HG04228.hp1 NA18951.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+8354C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988442 | |||||||
chr1:84988493 | C | T | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+8303G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988493 | |||||||
chr1:84988495 | C | G | 1 | a0003c0003t0005g0002 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.77+8301G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988495 | |||||||
chr1:84988545 | C | A | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+8251G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988545 | |||||||
chr1:84988731 | G | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(320): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.77+8065C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988731 | |||||||
chr1:84988764 | A | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+8032T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988764 | |||||||
chr1:84988918 | T | C | 7 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(4): Show |
7 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+7878A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988918 | |||||||
chr1:84988918 | T | G | 1 | a0004c0004t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+7878A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988918 | |||||||
chr1:84988919 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.77+7877G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988919 | |||||||
chr1:84988930 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7866A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84988930 | |||||||
chr1:84989198 | C | G | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7598G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989198 | |||||||
chr1:84989325 | T | C | 1 | a0001c0001t0009g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.77+7471A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989325 | |||||||
chr1:84989679 | A | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7117T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989679 | |||||||
chr1:84989689 | C | A | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7107G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989689 | |||||||
chr1:84989690 | A | T | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+7106T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989690 | |||||||
chr1:84989845 | T | C | 3 | a0001c0001t0004g0093 a0001c0001t0004g0094 a0001c0001t0004g0096 |
3 | NA18966.hp2 NA18967.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.77+6951A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989845 | |||||||
chr1:84989849 | C | T | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6947G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989849 | |||||||
chr1:84989993 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.77+6803A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84989993 | |||||||
chr1:84990019 | G | A | 11 | a0001c0001t0002g0242 a0001c0001t0002g0247 a0001c0001t0003g0008 others(8): Show |
14 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.77+6777C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990019 | |||||||
chr1:84990024 | T | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6772A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990024 | |||||||
chr1:84990140 | C | CA | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6655dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990140 | |||||||
chr1:84990142 | A | C | 87 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(84): Show |
91 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.77+6654T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990142 | |||||||
chr1:84990213 | G | T | 1 | a0001c0001t0004g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.77+6583C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990213 | |||||||
chr1:84990230 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.77+6566C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990230 | |||||||
chr1:84990253 | G | C | 77 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.77+6543C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990253 | |||||||
chr1:84990297 | C | CA | 32 | a0001c0001t0001g0059 a0001c0001t0001g0072 a0001c0001t0001g0081 others(29): Show |
32 | HG00597.hp2 HG01099.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.77+6498dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | |||||||
chr1:84990297 | CA | C | 81 | a0001c0001t0001g0084 a0001c0001t0001g0108 a0001c0001t0001g0175 others(78): Show |
86 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.77+6498delT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | |||||||
chr1:84990297 | CAAA | C | 10 | a0001c0001t0002g0193 a0001c0001t0002g0280 a0001c0001t0002g0281 others(7): Show |
10 | HG00558.hp1 HG00642.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+6496_77+6498del others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | |||||||
chr1:84990297 | CAAAA | C | 54 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0235 others(51): Show |
59 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.77+6495_77+6498del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | |||||||
chr1:84990297 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0293 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.77+6487_77+6498del others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | |||||||
chr1:84990297 | CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0002g0290 a0001c0001t0002g0292 a0001c0001t0003g0249 others(9): Show |
12 | HG02015.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.77+6486_77+6498del others(13): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990297 | |||||||
chr1:84990328 | T | A | 2 | a0001c0001t0001g0116 a0001c0001t0007g0117 |
2 | NA18967.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.77+6468A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990328 | |||||||
chr1:84990436 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.77+6360A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990436 | |||||||
chr1:84990446 | T | TA | 76 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(73): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+6349dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990446 | |||||||
chr1:84990447 | A | T | 1 | a0001c0001t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.77+6349T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990447 | |||||||
chr1:84990508 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0007g0119 a0001c0001t0020g0090 |
3 | HG01993.hp2 NA18974.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.77+6288A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990508 | |||||||
chr1:84990523 | C | T | 7 | a0001c0001t0013g0028 a0003c0003t0005g0002 a0003c0003t0005g0030 others(4): Show |
8 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+6273G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990523 | |||||||
chr1:84990641 | G | C | 4 | a0004c0004t0001g0046 a0006c0005t0001g0044 a0006c0005t0001g0045 others(1): Show |
4 | HG02615.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6155C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990641 | |||||||
chr1:84990813 | A | T | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.77+5983T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990813 | |||||||
chr1:84990826 | TG | T | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.77+5969delC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990826 | |||||||
chr1:84990906 | G | A | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5890C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990906 | |||||||
chr1:84990942 | A | G | 5 | a0001c0001t0002g0290 a0001c0001t0002g0292 a0001c0001t0003g0249 others(2): Show |
5 | HG02015.hp1 NA18961.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+5854T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84990942 | |||||||
chr1:84991096 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.77+5700C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991096 | |||||||
chr1:84991219 | T | C | 67 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(64): Show |
72 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.77+5577A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991219 | |||||||
chr1:84991278 | T | G | 67 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(64): Show |
72 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.77+5518A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991278 | |||||||
chr1:84991383 | C | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.77+5413G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991383 | |||||||
chr1:84991400 | C | T | 1 | a0001c0001t0026g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.77+5396G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991400 | |||||||
chr1:84991604 | A | G | 1 | a0001c0001t0005g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.77+5192T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991604 | |||||||
chr1:84991678 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.77+5118A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84991678 | |||||||
chr1:84992248 | C | G | 1 | a0007c0010t0002g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.77+4548G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992248 | |||||||
chr1:84992250 | C | G | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+4546G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992250 | |||||||
chr1:84992372 | C | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0004g0148 others(2): Show |
5 | HG00558.hp2 NA18960.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+4424G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992372 | |||||||
chr1:84992374 | C | T | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+4422G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992374 | |||||||
chr1:84992400 | A | T | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+4396T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992400 | |||||||
chr1:84992402 | A | G | 2 | a0001c0001t0031g0246 a0007c0010t0002g0245 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+4394T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992402 | |||||||
chr1:84992435 | A | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.77+4361T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992435 | |||||||
chr1:84992465 | C | T | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+4331G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992465 | |||||||
chr1:84992752 | T | TA | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.77+4043dupT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992752 | |||||||
chr1:84992759 | A | AC | 76 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(73): Show |
77 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.77+4036dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992759 | |||||||
chr1:84992879 | T | TC | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+3916dupG | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84992879 | |||||||
chr1:84993063 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.77+3733G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993063 | |||||||
chr1:84993179 | G | T | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+3617C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993179 | |||||||
chr1:84993309 | G | A | 1 | a0004c0004t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+3487C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993309 | |||||||
chr1:84993325 | T | C | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+3471A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993325 | |||||||
chr1:84993380 | T | G | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+3416A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993380 | |||||||
chr1:84993505 | T | C | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+3291A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993505 | |||||||
chr1:84993506 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.77+3290C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993506 | |||||||
chr1:84993515 | G | A | 159 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(156): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.77+3281C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993515 | |||||||
chr1:84993575 | G | T | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+3221C>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993575 | |||||||
chr1:84993616 | T | TAA | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.77+3179_77+3180ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993616 | |||||||
chr1:84993616 | T | TAG | 159 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(156): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.77+3179_77+3180ins others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993616 | |||||||
chr1:84993617 | G | A | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3179C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993617 | |||||||
chr1:84993618 | T | G | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3178A>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993618 | |||||||
chr1:84993619 | C | CT | 16 | a0001c0001t0001g0061 a0001c0001t0001g0074 a0001c0001t0001g0125 others(13): Show |
16 | HG01106.hp2 HG01346.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+3176dupA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993619 | |||||||
chr1:84993619 | C | G | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3177G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993619 | |||||||
chr1:84993619 | CTTT | C | 164 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(161): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.77+3174_77+3176del others(3): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993619 | |||||||
chr1:84993621 | T | C | 1 | a0001c0001t0006g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.77+3175A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993621 | |||||||
chr1:84993672 | G | A | 1 | a0001c0001t0006g0234 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.77+3124C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993672 | |||||||
chr1:84993716 | C | T | 3 | a0001c0001t0004g0049 a0001c0001t0004g0099 a0001c0001t0004g0181 |
3 | HG00735.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.77+3080G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993716 | |||||||
chr1:84993742 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+3054A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993742 | |||||||
chr1:84993786 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.77+3010T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993786 | |||||||
chr1:84993791 | C | T | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+3005G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993791 | |||||||
chr1:84993792 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.77+3004C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993792 | |||||||
chr1:84993868 | G | A | 1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+2928C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993868 | |||||||
chr1:84993882 | G | A | 6 | a0001c0001t0031g0246 a0004c0004t0001g0041 a0004c0004t0001g0042 others(3): Show |
6 | HG00642.hp2 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+2914C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993882 | |||||||
chr1:84993893 | G | A | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+2903C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84993893 | |||||||
chr1:84994047 | C | T | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+2749G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994047 | |||||||
chr1:84994048 | A | G | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+2748T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994048 | |||||||
chr1:84994065 | T | C | 2 | a0001c0001t0031g0246 a0007c0010t0002g0245 |
2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.77+2731A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994065 | |||||||
chr1:84994086 | A | G | 8 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0046 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+2710T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994086 | |||||||
chr1:84994338 | T | C | 66 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(63): Show |
71 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.77+2458A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994338 | |||||||
chr1:84994354 | CCTCT | C | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+2438_77+2441del others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994354 | |||||||
chr1:84994390 | C | T | 1 | a0001c0001t0007g0098 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.77+2406G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994390 | |||||||
chr1:84994442 | CCTTCATC others(6): Show |
C | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.77+2341_77+2353del others(13): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994442 | |||||||
chr1:84994464 | C | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.77+2332G>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994464 | |||||||
chr1:84994820 | C | T | 1 | a0001c0001t0009g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.77+1976G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994820 | |||||||
chr1:84994876 | C | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0009g0178 others(2): Show |
5 | HG00673.hp2 NA18968.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+1920G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84994876 | |||||||
chr1:84995203 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.77+1593T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995203 | |||||||
chr1:84995229 | C | A | 168 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(165): Show |
177 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.77+1567G>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995229 | |||||||
chr1:84995239 | T | C | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+1557A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995239 | |||||||
chr1:84995248 | A | G | 8 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0078 others(5): Show |
8 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+1548T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995248 | |||||||
chr1:84995262 | CT | C | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+1533delA | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995262 | |||||||
chr1:84995283 | T | C | 1 | a0001c0001t0001g0007 | 2 | NA18964.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.77+1513A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995283 | |||||||
chr1:84995347 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.77+1449T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995347 | |||||||
chr1:84995469 | G | C | 1 | a0001c0001t0002g0247 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.77+1327C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995469 | |||||||
chr1:84995573 | C | T | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+1223G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995573 | |||||||
chr1:84995586 | AG | A | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+1209delC | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995586 | |||||||
chr1:84995724 | C | T | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+1072G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995724 | |||||||
chr1:84995804 | T | A | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | HG02135.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.77+992A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | |||||||
chr1:84995804 | T | TA | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0006g0184 |
3 | HG02155.hp1 NA18974.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.77+991_77+992insT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | |||||||
chr1:84995804 | T | TAA | 15 | a0001c0001t0002g0237 a0001c0001t0002g0242 a0001c0001t0002g0247 others(12): Show |
18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+991_77+992insTT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | |||||||
chr1:84995804 | T | TAAA | 33 | a0001c0001t0002g0290 a0001c0001t0002g0292 a0001c0001t0002g0294 others(30): Show |
34 | HG00597.hp1 HG01243.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.77+991_77+992insTT others(1): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | |||||||
chr1:84995804 | T | TAAAA | 9 | a0001c0001t0002g0320 a0001c0001t0002g0322 a0001c0001t0002g0323 others(6): Show |
9 | HG00609.hp2 HG00741.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+991_77+992insTT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995804 | |||||||
chr1:84995805 | T | A | 62 | a0001c0001t0002g0237 a0001c0001t0002g0242 a0001c0001t0002g0247 others(59): Show |
66 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.77+991A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995805 | |||||||
chr1:84995805 | T | TAAA | 41 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(38): Show |
41 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.77+990_77+991insTT others(1): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995805 | |||||||
chr1:84995805 | T | TAAAA | 52 | a0001c0001t0002g0015 a0001c0001t0002g0248 a0001c0001t0002g0250 others(49): Show |
57 | HG00280.hp2 HG00558.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.77+990_77+991insTT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995805 | |||||||
chr1:84995806 | T | A | 157 | a0001c0001t0002g0015 a0001c0001t0002g0192 a0001c0001t0002g0193 others(154): Show |
166 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.77+990A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995806 | |||||||
chr1:84995807 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.77+989T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995807 | |||||||
chr1:84995869 | T | A | 4 | a0004c0004t0001g0041 a0004c0004t0001g0042 a0004c0004t0001g0048 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+927A>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995869 | |||||||
chr1:84995981 | A | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG02040.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.77+815T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84995981 | |||||||
chr1:84996030 | A | C | 1 | a0001c0001t0003g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.77+766T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996030 | |||||||
chr1:84996113 | A | G | 1 | a0001c0001t0005g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.77+683T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996113 | |||||||
chr1:84996179 | A | C | 1 | a0001c0001t0003g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.77+617T>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996179 | |||||||
chr1:84996263 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.77+533T>C | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996263 | |||||||
chr1:84996292 | T | C | 6 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0002g0326 others(3): Show |
6 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+504A>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996292 | |||||||
chr1:84996393 | C | CAT | 10 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(7): Show |
10 | HG00323.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+401_77+402dupAT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATAT | 8 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0004g0083 others(5): Show |
8 | HG01993.hp2 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.77+399_77+402dupAT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATAT | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+397_77+402dupAT others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(1): Show |
5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG02109.hp1 HG02809.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+395_77+402dupAT others(6): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(3): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
6 | HG01109.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+393_77+402dupAT others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(5): Show |
6 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
6 | HG01106.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+391_77+402dupAT others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(7): Show |
6 | a0001c0001t0001g0061 a0001c0001t0004g0049 a0001c0001t0007g0062 others(3): Show |
6 | HG00735.hp2 HG01346.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+389_77+402dupAT others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(9): Show |
5 | a0001c0001t0001g0059 a0001c0001t0007g0058 a0002c0002t0001g0060 others(2): Show |
5 | HG02683.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+387_77+402dupAT others(14): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(11): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01099.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.77+385_77+402dupAT others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(13): Show |
4 | a0001c0001t0001g0054 a0002c0002t0001g0055 a0004c0004t0001g0042 others(1): Show |
4 | HG02572.hp2 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+383_77+402dupAT others(18): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | C | CATATATA others(15): Show |
2 | a0001c0001t0007g0053 a0004c0004t0001g0041 |
2 | HG02257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.77+381_77+402dupAT others(20): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CAT | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0108 a0001c0001t0001g0111 others(14): Show |
18 | HG00621.hp2 HG01070.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+401_77+402delAT | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATAT | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02886.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+399_77+402delAT others(2): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATAT | C | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0005g0029 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+397_77+402delAT others(4): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(3): Show |
C | 11 | a0001c0001t0004g0129 a0001c0001t0004g0130 a0001c0001t0004g0131 others(8): Show |
11 | HG00140.hp2 HG01081.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.77+393_77+402delAT others(8): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(5): Show |
C | 1 | a0001c0001t0005g0040 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.77+391_77+402delAT others(10): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(7): Show |
C | 1 | a0005c0006t0001g0132 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.77+389_77+402delAT others(12): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0134 a0001c0001t0028g0135 a0005c0006t0024g0133 |
3 | HG01099.hp2 HG03209.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.77+385_77+402delAT others(16): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(13): Show |
C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
55 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.77+383_77+402delAT others(18): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(17): Show |
C | 4 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0004g0179 others(1): Show |
4 | HG02155.hp1 HG03453.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+379_77+402delAT others(22): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996393 | CATATATA others(19): Show |
C | 157 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(154): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.77+377_77+402delAT others(24): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996393 | |||||||
chr1:84996429 | T | TATATATA others(4): Show |
1 | a0010c0009t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.77+366_77+367insTA others(9): Show |
MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996429 | |||||||
chr1:84996449 | C | T | 3 | a0001c0001t0009g0050 a0001c0001t0009g0051 a0001c0001t0009g0052 |
3 | NA18747.hp1 NA18979.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.77+347G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996449 | |||||||
chr1:84996511 | G | C | 160 | a0001c0001t0002g0015 a0001c0001t0002g0189 a0001c0001t0002g0191 others(157): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.77+285C>G | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996511 | |||||||
chr1:84996520 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.77+276G>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996520 | |||||||
chr1:84996563 | G | A | 1 | a0001c0001t0004g0181 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.77+233C>T | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996563 | |||||||
chr1:84996619 | A | T | 1 | a0001c0001t0014g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.77+177T>A | MCOLN2 | ENSG00000153898.13 | transcript | ENST00000370608.8 | protein_coding | 1/13 | chr1 | 84996619 |