Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26504 |
| ensemblid | ENSG00000158158.12 |
| hgncid | 105 |
| symbol | CNNM4 |
| name | cyclin and CBS domain divalent metal cation transport mediator 4 |
| refseq_nuc | NM_020184.4 |
| refseq_prot | NP_064569.3 |
| ensembl_nuc | ENST00000377075.3 |
| ensembl_prot | ENSP00000366275.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 96760902 |
| end | 96811874 |
| strand | + |
| ver | v1.2 |
| region | chr2:96760902-96811874 |
| region5000 | chr2:96755902-96816874 |
| regionname0 | CNNM4_chr2_96760902_96811874 |
| regionname5000 | CNNM4_chr2_96755902_96816874 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 775 | 265 | 84 | 55 | 94 | 12 | 18 | 68 | CNNM4_chr2_96755902_96816874 | CNNM4 | MAPVG others(770): Show |
chr2 | 96755902 | 96816874 |
| a0002 | 0/0 | 775 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | MAPVG others(770): Show |
chr2 | 96755902 | 96816874 |
| a0003 | 0/0 | 775 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | MAPVG others(770): Show |
chr2 | 96755902 | 96816874 |
| a0004 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | MAPVG others(770): Show |
chr2 | 96755902 | 96816874 |
| a0005 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | MAPVG others(770): Show |
chr2 | 96755902 | 96816874 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2325 | 252 | 74 | 53 | 93 | 12 | 18 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0001c0002 | 0/0 | 2325 | 9 | 9 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0001c0003 | 0/0 | 2325 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0001c0008 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0001c0009 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0002c0004 | 0/0 | 2325 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0003c0006 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0004c0007 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 | ||
| a0005c0005 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | ATGGC others(2320): Show |
chr2 | 96755902 | 96816874 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4783 | 146 | 10 | 40 | 69 | 11 | 14 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0002 | 0/0 | 4783 | 37 | 20 | 2 | 13 | 0 | 2 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0003 | 0/0 | 4783 | 27 | 8 | 9 | 9 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0004 | 0/0 | 4783 | 19 | 19 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0005 | 0/0 | 4783 | 4 | 4 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0006 | 0/0 | 4783 | 7 | 6 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0007 | 0/0 | 4783 | 3 | 3 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0008 | 0/0 | 4780 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4775): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0009 | 0/0 | 4783 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0010 | 0/0 | 4783 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0011 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0012 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0013 | 0/0 | 4783 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0014 | 0/0 | 4783 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0001t0015 | 0/0 | 4783 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0002t0005 | 0/0 | 4783 | 9 | 9 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0003t0001 | 0/0 | 4783 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0008t0002 | 0/0 | 4783 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0001c0009t0007 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0002c0004t0003 | 0/0 | 4783 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0003c0006t0001 | 0/0 | 4783 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0004c0007t0002 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| a0005c0005t0006 | 0/0 | 4783 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | AGTTG others(4778): Show |
chr2 | 96755902 | 96816874 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 3 | 0 | 0 | 0 | 2 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0001t0015g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0002t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0008t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0001c0009t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0002c0004t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0002c0004t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0003c0006t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0004c0007t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| a0005c0005t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01074 | hp2 | a0003 | c0006 | t0001 | g0253 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0248 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01175 | hp1 | a0001 | c0001 | t0015 | g0240 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0135 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0114 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02145 | hp2 | a0001 | c0009 | t0007 | g0191 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0137 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | PEL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02809 | hp1 | a0002 | c0004 | t0003 | g0100 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02895 | hp2 | a0002 | c0004 | t0003 | g0101 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0031 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02922 | hp2 | a0004 | c0007 | t0002 | g0155 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0133 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0098 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03130 | hp2 | a0005 | c0005 | t0006 | g0231 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0139 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03195 | hp2 | a0001 | c0002 | t0005 | g0074 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0138 | AFR | ESN | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0263 | AFR | MSL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18951 | hp1 | a0001 | c0001 | t0010 | g0125 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18983 | hp2 | a0001 | c0008 | t0002 | g0029 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0237 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19064 | hp2 | a0001 | c0001 | t0013 | g0106 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | YRI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | ASW | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | ASW | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0003 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0134 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | USA | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | LWK | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0190 | REF | REF | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CNNM4_chr2_96755902_96816874 | CNNM4 | chr2 | 96755902 | 96816874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96761547 | G | C | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.548G>C | p.Trp183Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 646/4783 | 548/2328 | 183/775 | chr2 | 96761547 | |||
| chr2:96761787 | A | G | 1 | a0002 | 2 | HG02809.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.788A>G | p.Asn263Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 886/4783 | 788/2328 | 263/775 | chr2 | 96761787 | |||
| chr2:96799603 | G | A | 1 | a0003 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1903G>A | p.Ala635Thr | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/7 | 2001/4783 | 1903/2328 | 635/775 | chr2 | 96799603 | |||
| chr2:96809330 | A | T | 1 | a0004 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.2141A>T | p.Gln714Leu | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2239/4783 | 2141/2328 | 714/775 | chr2 | 96809330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96761962 | C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.963C>T | p.Ser321Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 1061/4783 | 963/2328 | 321/775 | chr2 | 96761962 | |||
| chr2:96762340 | C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1341C>T | p.His447His | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | 1439/4783 | 1341/2328 | 447/775 | chr2 | 96762340 | |||
| chr2:96799199 | G | A | 1 | a0001c0002 | 9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.1824G>A | p.Pro608Pro | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 4/7 | 1922/4783 | 1824/2328 | 608/775 | chr2 | 96799199 | |||
| chr2:96799602 | C | T | 1 | a0001c0008 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1902C>T | p.Gly634Gly | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/7 | 2000/4783 | 1902/2328 | 634/775 | chr2 | 96799602 | |||
| chr2:96799647 | C | T | 1 | a0001c0003 | 2 | HG01081.hp1 HG02300.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1947C>T | p.Ser649Ser | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/7 | 2045/4783 | 1947/2328 | 649/775 | chr2 | 96799647 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96760946 | C | T | 1 | a0001c0001t0015 | 1 | HG01175.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/7 | chr2 | 96760946 | |||||||
| chr2:96809608 | C | T | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0005 |
32 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 91 | chr2 | 96809608 | ||||||
| chr2:96809612 | T | C | 1 | a0001c0001t0009 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 95 | chr2 | 96809612 | ||||||
| chr2:96809975 | TTCC | T | 1 | a0001c0001t0008 | 2 | HG02970.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*477_*479delTCC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 477 | INFO_REALIGN_3_PRIME | chr2 | 96809975 | |||||
| chr2:96810270 | G | A | 1 | a0001c0001t0010 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 753 | chr2 | 96810270 | ||||||
| chr2:96810482 | A | G | 4 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(1): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 965 | chr2 | 96810482 | ||||||
| chr2:96810576 | T | C | 1 | a0001c0001t0010 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1059 | chr2 | 96810576 | ||||||
| chr2:96810761 | C | T | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0012 others(1): Show |
33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1244C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1244 | chr2 | 96810761 | ||||||
| chr2:96810999 | C | T | 2 | a0001c0001t0006 a0005c0005t0006 |
8 | HG00642.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1482C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1482 | chr2 | 96810999 | ||||||
| chr2:96811033 | C | T | 2 | a0001c0001t0007 a0001c0009t0007 |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1516C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1516 | chr2 | 96811033 | ||||||
| chr2:96811210 | G | A | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0005 |
32 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1693G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1693 | chr2 | 96811210 | ||||||
| chr2:96811507 | T | A | 2 | a0001c0001t0005 a0001c0002t0005 |
13 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1990T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 1990 | chr2 | 96811507 | ||||||
| chr2:96811637 | C | T | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
113 | HG00609.hp1 HG00642.hp1 HG01070.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2120C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2120 | chr2 | 96811637 | ||||||
| chr2:96811842 | T | C | 1 | a0001c0001t0011 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2325T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2325 | chr2 | 96811842 | ||||||
| chr2:96811847 | T | G | 1 | a0001c0001t0014 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2330T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 7/7 | 2330 | chr2 | 96811847 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:96762583 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(68): Show |
72 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1402+182G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762583 | |||||||
| chr2:96762638 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1402+237C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762638 | |||||||
| chr2:96762725 | G | A | 1 | a0001c0002t0005g0074 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1402+324G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762725 | |||||||
| chr2:96762971 | C | T | 1 | a0001c0002t0005g0263 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1402+570C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96762971 | |||||||
| chr2:96763183 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1402+782C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763183 | |||||||
| chr2:96763258 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1402+857G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763258 | |||||||
| chr2:96763539 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1402+1138G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763539 | |||||||
| chr2:96763549 | G | A | 2 | a0001c0001t0006g0076 a0001c0001t0006g0077 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+1148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763549 | |||||||
| chr2:96763647 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1402+1246C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96763647 | |||||||
| chr2:96764196 | G | C | 3 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0006g0078 |
3 | HG00642.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1402+1795G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764196 | |||||||
| chr2:96764214 | T | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(246): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1402+1813T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764214 | |||||||
| chr2:96764483 | CT | C | 9 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1402+2083delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764483 | |||||||
| chr2:96764589 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+2188G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764589 | |||||||
| chr2:96764717 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02523.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1402+2316G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96764717 | |||||||
| chr2:96765014 | G | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02071.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1402+2613G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765014 | |||||||
| chr2:96765024 | G | GTT | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0241 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+2664_1402+266 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0006g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1402+2656_1402+266 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GT | G | 20 | a0001c0001t0001g0071 a0001c0001t0001g0218 a0001c0001t0001g0219 others(17): Show |
20 | HG00280.hp2 HG00673.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1402+2665delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTT | G | 33 | a0001c0001t0001g0012 a0001c0001t0001g0189 a0001c0001t0001g0192 others(30): Show |
33 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1402+2664_1402+266 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTT | G | 44 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(41): Show |
44 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1402+2663_1402+266 others(7): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTT | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0036 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1402+2662_1402+266 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTT | G | 22 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
22 | HG00741.hp2 HG01496.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1402+2661_1402+266 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTT | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
6 | HG01123.hp2 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+2660_1402+266 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0005g0141 a0001c0002t0005g0142 |
2 | HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1402+2656_1402+266 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0004g0136 a0001c0001t0005g0140 a0001c0002t0005g0137 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+2655_1402+266 others(15): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(5): Show |
G | 13 | a0001c0001t0004g0080 a0001c0001t0004g0126 a0001c0001t0004g0127 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1402+2654_1402+266 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0249 a0001c0001t0004g0079 a0001c0001t0004g0121 others(5): Show |
8 | HG00642.hp1 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+2653_1402+266 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 |
3 | HG02486.hp1 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1402+2652_1402+266 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0004g0115 a0001c0001t0004g0116 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1402+2651_1402+266 others(19): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0001g0013 a0001c0001t0012g0114 |
2 | HG00642.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1402+2650_1402+266 others(20): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(11): Show |
G | 1 | a0001c0003t0001g0248 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1402+2648_1402+266 others(22): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(12): Show |
G | 8 | a0001c0001t0002g0113 a0001c0001t0003g0089 a0001c0001t0003g0107 others(5): Show |
8 | HG01071.hp2 HG01981.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+2647_1402+266 others(23): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(13): Show |
G | 23 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(20): Show |
24 | HG01070.hp2 HG01099.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1402+2646_1402+266 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1402+2645_1402+266 others(25): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765024 | GTTTTTTT others(19): Show |
G | 3 | a0001c0001t0005g0092 a0001c0001t0006g0076 a0001c0001t0006g0077 |
3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+2640_1402+266 others(30): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765024 | ||||||
| chr2:96765032 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1402+2631T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765032 | |||||||
| chr2:96765037 | T | G | 1 | a0001c0001t0001g0011 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1402+2636T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765037 | |||||||
| chr2:96765038 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1402+2637T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765038 | |||||||
| chr2:96765100 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1402+2699C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765100 | |||||||
| chr2:96765134 | T | G | 2 | a0001c0001t0006g0076 a0001c0001t0006g0077 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+2733T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765134 | |||||||
| chr2:96765146 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0189 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1402+2745G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765146 | |||||||
| chr2:96765221 | G | T | 1 | a0001c0001t0013g0106 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1402+2820G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765221 | |||||||
| chr2:96765332 | G | A | 4 | a0001c0001t0006g0232 a0001c0001t0006g0233 a0001c0001t0006g0244 others(1): Show |
4 | HG03130.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402+2931G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765332 | |||||||
| chr2:96765372 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+2971C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765372 | |||||||
| chr2:96765424 | C | A | 30 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+3023C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765424 | |||||||
| chr2:96765489 | C | T | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1402+3088C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765489 | |||||||
| chr2:96765662 | A | G | 12 | a0001c0001t0005g0124 a0001c0001t0005g0140 a0001c0001t0005g0141 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+3261A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96765662 | |||||||
| chr2:96765777 | TTTTC | T | 43 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(40): Show |
44 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.1402+3396_1402+339 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96765777 | ||||||
| chr2:96766053 | G | A | 1 | a0001c0001t0008g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+3652G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766053 | |||||||
| chr2:96766090 | T | A | 1 | a0001c0001t0008g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1402+3689T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766090 | |||||||
| chr2:96766144 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+3743G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766144 | |||||||
| chr2:96766364 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1402+3963C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766364 | |||||||
| chr2:96766580 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0012g0114 |
3 | HG00280.hp1 HG00323.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1402+4179G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96766580 | |||||||
| chr2:96767390 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1402+4989G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96767390 | |||||||
| chr2:96767425 | A | C | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+5024A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96767425 | |||||||
| chr2:96767986 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1402+5585C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96767986 | |||||||
| chr2:96768098 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1402+5697A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768098 | |||||||
| chr2:96768324 | C | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(56): Show |
60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1402+5923C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768324 | |||||||
| chr2:96768357 | AG | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+5957delG | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768357 | |||||||
| chr2:96768548 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1402+6147C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768548 | |||||||
| chr2:96768877 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1402+6476G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96768877 | |||||||
| chr2:96769078 | T | C | 1 | a0001c0001t0008g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+6677T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769078 | |||||||
| chr2:96769397 | C | T | 8 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0128 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+6996C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769397 | |||||||
| chr2:96769457 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1402+7056G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769457 | |||||||
| chr2:96769458 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1402+7057C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769458 | |||||||
| chr2:96769563 | CA | C | 20 | a0001c0001t0001g0160 a0001c0001t0001g0216 a0001c0001t0004g0079 others(17): Show |
20 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1402+7179delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96769563 | ||||||
| chr2:96769760 | TG | T | 11 | a0001c0001t0005g0124 a0001c0001t0005g0141 a0001c0002t0005g0074 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+7360delG | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769760 | |||||||
| chr2:96769782 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1402+7381A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769782 | |||||||
| chr2:96769813 | G | A | 2 | a0001c0001t0006g0244 a0005c0005t0006g0231 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1402+7412G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769813 | |||||||
| chr2:96769820 | G | A | 30 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+7419G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96769820 | |||||||
| chr2:96770149 | A | T | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1402+7748A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770149 | |||||||
| chr2:96770310 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1402+7909C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770310 | |||||||
| chr2:96770471 | G | A | 3 | a0001c0001t0004g0121 a0001c0001t0004g0126 a0001c0001t0004g0127 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+8070G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770471 | |||||||
| chr2:96770532 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1402+8131G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770532 | |||||||
| chr2:96770555 | C | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+8154C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770555 | |||||||
| chr2:96770653 | C | T | 12 | a0001c0001t0005g0124 a0001c0001t0005g0140 a0001c0001t0005g0141 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+8252C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770653 | |||||||
| chr2:96770871 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1402+8470C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96770871 | |||||||
| chr2:96771091 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1402+8690A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771091 | |||||||
| chr2:96771144 | C | A | 1 | a0001c0001t0008g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+8743C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771144 | |||||||
| chr2:96771193 | G | A | 4 | a0001c0001t0007g0164 a0001c0001t0007g0165 a0001c0001t0007g0166 others(1): Show |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1402+8792G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771193 | |||||||
| chr2:96771272 | ATT | A | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1402+8872_1402+887 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771272 | |||||||
| chr2:96771275 | C | A | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1402+8874C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771275 | |||||||
| chr2:96771292 | T | C | 1 | a0003c0006t0001g0253 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1402+8891T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771292 | |||||||
| chr2:96771293 | CT | C | 8 | a0001c0001t0001g0167 a0001c0001t0004g0115 a0001c0001t0004g0116 others(5): Show |
8 | HG00323.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1402+8907delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96771293 | ||||||
| chr2:96771475 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1402+9074C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771475 | |||||||
| chr2:96771610 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1402+9209A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96771610 | |||||||
| chr2:96771713 | C | CA | 40 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0192 others(37): Show |
41 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1402+9326dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96771713 | ||||||
| chr2:96772059 | C | T | 1 | a0001c0001t0006g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1402+9658C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772059 | |||||||
| chr2:96772253 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(160): Show |
166 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1402+9852T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772253 | |||||||
| chr2:96772341 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+9940C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772341 | |||||||
| chr2:96772375 | GTGCGCAC others(48): Show |
G | 1 | a0001c0001t0010g0125 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1402+9992_1402+100 others(60): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96772375 | ||||||
| chr2:96772379 | G | A | 5 | a0001c0001t0001g0169 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00423.hp2 NA18612.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402+9978G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772379 | |||||||
| chr2:96772427 | C | G | 1 | a0001c0001t0008g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1402+10026C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772427 | |||||||
| chr2:96772474 | G | A | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1402+10073G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772474 | |||||||
| chr2:96772549 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1402+10148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772549 | |||||||
| chr2:96772609 | GCACACAC others(57): Show |
G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0196 a0001c0001t0001g0238 |
3 | HG00323.hp1 HG01106.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1402+10327_1402+10 others(70): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96772609 | ||||||
| chr2:96772624 | C | A | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1402+10223C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772624 | |||||||
| chr2:96772659 | A | G | 5 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+10258A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772659 | |||||||
| chr2:96772726 | CGTGCACA others(55): Show |
C | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1402+10327_1402+10 others(68): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96772726 | ||||||
| chr2:96772745 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1402+10344A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772745 | |||||||
| chr2:96772791 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1402+10390G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772791 | |||||||
| chr2:96772815 | G | C | 59 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(56): Show |
60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1402+10414G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96772815 | |||||||
| chr2:96773062 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1402+10661C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773062 | |||||||
| chr2:96773261 | T | G | 1 | a0001c0001t0001g0234 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1402+10860T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773261 | |||||||
| chr2:96773264 | A | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1402+10863A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773264 | |||||||
| chr2:96773338 | G | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG00733.hp1 HG01192.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1402+10937G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773338 | |||||||
| chr2:96773488 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1402+11087T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773488 | |||||||
| chr2:96773653 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1402+11252G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773653 | |||||||
| chr2:96773658 | C | G | 1 | a0001c0003t0001g0260 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1402+11257C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773658 | |||||||
| chr2:96773796 | TCATGCCA others(8): Show |
T | 1 | a0001c0001t0002g0068 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1402+11398_1402+11 others(21): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773796 | ||||||
| chr2:96773819 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1402+11418G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96773819 | |||||||
| chr2:96773841 | T | TA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0197 others(3): Show |
6 | HG01123.hp2 HG01255.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+11458dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773841 | ||||||
| chr2:96773841 | TA | T | 61 | a0001c0001t0001g0033 a0001c0001t0001g0171 a0001c0001t0001g0185 others(58): Show |
62 | HG00558.hp2 HG00642.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.1402+11458delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773841 | ||||||
| chr2:96773899 | AAAT | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(46): Show |
50 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1402+11501_1402+11 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96773899 | ||||||
| chr2:96774090 | C | T | 12 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(9): Show |
12 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+11689C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774090 | |||||||
| chr2:96774400 | C | T | 3 | a0001c0001t0004g0121 a0001c0001t0004g0126 a0001c0001t0004g0127 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+11999C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774400 | |||||||
| chr2:96774428 | A | T | 3 | a0001c0001t0004g0121 a0001c0001t0004g0126 a0001c0001t0004g0127 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+12027A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774428 | |||||||
| chr2:96774477 | G | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1402+12076G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774477 | |||||||
| chr2:96774683 | G | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+12282G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774683 | |||||||
| chr2:96774830 | G | A | 30 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+12429G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774830 | |||||||
| chr2:96774960 | C | CA | 11 | a0001c0001t0001g0040 a0001c0001t0001g0168 a0001c0001t0001g0172 others(8): Show |
11 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+12597dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CA | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
64 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1402+12597delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAA | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(49): Show |
53 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1402+12596_1402+12 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAA | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
6 | NA18612.hp2 NA18957.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+12595_1402+12 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAA | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0184 others(4): Show |
7 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1402+12593_1402+12 others(11): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0214 a0001c0001t0001g0243 others(14): Show |
17 | HG01123.hp2 HG01261.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1402+12591_1402+12 others(13): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0213 a0001c0001t0002g0006 a0001c0001t0002g0007 others(3): Show |
6 | HG00099.hp1 HG02630.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1402+12590_1402+12 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0003g0081 a0001c0001t0003g0094 a0001c0001t0003g0095 others(6): Show |
9 | HG01123.hp1 HG02257.hp2 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.1402+12589_1402+12 others(15): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(3): Show |
C | 22 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0082 others(19): Show |
23 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1402+12588_1402+12 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(4): Show |
C | 11 | a0001c0001t0003g0088 a0001c0001t0004g0123 a0001c0001t0004g0128 others(8): Show |
11 | HG01256.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+12587_1402+12 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(5): Show |
C | 15 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(12): Show |
15 | HG00642.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1402+12586_1402+12 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0006g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1402+12585_1402+12 others(19): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0262 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1402+12583_1402+12 others(21): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0159 a0001c0001t0006g0076 |
2 | HG01891.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1402+12581_1402+12 others(23): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0005g0092 a0001c0001t0006g0077 |
2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+12580_1402+12 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774960 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0252 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1402+12579_1402+12 others(25): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96774960 | ||||||
| chr2:96774998 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1402+12597A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96774998 | |||||||
| chr2:96775529 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(246): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1402+13128G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775529 | |||||||
| chr2:96775559 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1402+13158C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775559 | |||||||
| chr2:96775592 | G | C | 1 | a0001c0001t0004g0117 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1402+13191G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775592 | |||||||
| chr2:96775719 | GTGTTTTG others(4): Show |
G | 1 | a0001c0001t0001g0188 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1402+13336_1402+13 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96775719 | ||||||
| chr2:96775721 | G | GTTTTGTT others(10): Show |
1 | a0003c0006t0001g0253 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1402+13338_1402+13 others(23): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96775721 | ||||||
| chr2:96775788 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG00558.hp1 NA18747.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402+13387T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775788 | |||||||
| chr2:96775906 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1402+13505A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96775906 | |||||||
| chr2:96776027 | G | GT | 24 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0061 others(21): Show |
24 | HG00423.hp2 HG00673.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1402+13645dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96776027 | ||||||
| chr2:96776027 | GT | G | 5 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0194 others(2): Show |
5 | HG00544.hp1 HG03017.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402+13645delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96776027 | ||||||
| chr2:96776107 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1402+13706C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776107 | |||||||
| chr2:96776177 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+13776A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776177 | |||||||
| chr2:96776307 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0113 |
2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1402+13906C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776307 | |||||||
| chr2:96776345 | T | A | 1 | a0001c0001t0008g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1402+13944T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776345 | |||||||
| chr2:96776653 | G | A | 31 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1402+14252G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776653 | |||||||
| chr2:96776992 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1402+14591A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96776992 | |||||||
| chr2:96777042 | C | T | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1402+14641C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777042 | |||||||
| chr2:96777081 | C | T | 30 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1402+14680C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777081 | |||||||
| chr2:96777107 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0221 |
2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1402+14706G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777107 | |||||||
| chr2:96777169 | C | T | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1402+14768C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777169 | |||||||
| chr2:96777246 | C | G | 1 | a0001c0001t0006g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1402+14845C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777246 | |||||||
| chr2:96777265 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1402+14864C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777265 | |||||||
| chr2:96777387 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1402+14986C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777387 | |||||||
| chr2:96777661 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1402+15260C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777661 | |||||||
| chr2:96777662 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
5 | HG03225.hp2 NA18522.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402+15261G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777662 | |||||||
| chr2:96777807 | T | C | 2 | a0001c0001t0004g0128 a0001c0001t0004g0136 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402+15406T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96777807 | |||||||
| chr2:96778176 | T | G | 11 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(8): Show |
11 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+15775T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778176 | |||||||
| chr2:96778556 | CA | C | 30 | a0001c0001t0001g0255 a0001c0001t0002g0157 a0001c0001t0004g0079 others(27): Show |
30 | HG00642.hp1 HG01261.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1402+16171delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96778556 | ||||||
| chr2:96778695 | T | TC | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(84): Show |
88 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1402+16296dupC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96778695 | ||||||
| chr2:96778801 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1402+16400C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778801 | |||||||
| chr2:96778837 | T | C | 11 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(8): Show |
11 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+16436T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778837 | |||||||
| chr2:96778863 | A | G | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1402+16462A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778863 | |||||||
| chr2:96778987 | C | T | 3 | a0001c0001t0005g0092 a0001c0001t0006g0076 a0001c0001t0006g0077 |
3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1402+16586C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96778987 | |||||||
| chr2:96779236 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1402+16835G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779236 | |||||||
| chr2:96779352 | T | C | 2 | a0001c0001t0003g0082 a0001c0001t0003g0089 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1402+16951T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779352 | |||||||
| chr2:96779508 | C | CA | 38 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0059 others(35): Show |
38 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1402+17129dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | ||||||
| chr2:96779508 | C | CAA | 22 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0084 others(19): Show |
23 | HG01099.hp1 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1402+17128_1402+17 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | ||||||
| chr2:96779508 | C | CAAA | 11 | a0001c0001t0003g0075 a0001c0001t0003g0081 a0001c0001t0003g0082 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402+17127_1402+17 others(9): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | ||||||
| chr2:96779508 | CA | C | 13 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0247 others(10): Show |
13 | HG00323.hp1 HG02630.hp2 HG03453.hp2 others(10): Show |
intron_variant | MODIFIER | c.1402+17129delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779508 | ||||||
| chr2:96779806 | AT | A | 31 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1403-17190delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96779806 | ||||||
| chr2:96779917 | C | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1403-17095C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779917 | |||||||
| chr2:96779949 | C | T | 5 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-17063C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779949 | |||||||
| chr2:96779990 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1403-17022C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96779990 | |||||||
| chr2:96780137 | T | C | 1 | a0001c0001t0002g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1403-16875T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96780137 | |||||||
| chr2:96780419 | CT | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0001g0172 others(3): Show |
6 | HG02897.hp1 HG03017.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1403-16576delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780419 | ||||||
| chr2:96780506 | C | T | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-16506C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96780506 | |||||||
| chr2:96780905 | A | AT | 13 | a0001c0001t0001g0264 a0001c0001t0002g0143 a0001c0001t0002g0144 others(10): Show |
13 | HG01261.hp2 HG01358.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1403-16094dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780905 | ||||||
| chr2:96780966 | C | T | 15 | a0001c0001t0004g0121 a0001c0001t0004g0126 a0001c0001t0004g0127 others(12): Show |
15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1403-16046C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96780966 | |||||||
| chr2:96780972 | C | CT | 28 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0050 others(25): Show |
28 | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1403-16016dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780972 | ||||||
| chr2:96780972 | CT | C | 10 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0093 others(7): Show |
10 | HG00558.hp1 HG01070.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403-16016delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96780972 | ||||||
| chr2:96781022 | A | G | 1 | a0004c0007t0002g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1403-15990A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781022 | |||||||
| chr2:96781118 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0221 |
2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1403-15894A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781118 | |||||||
| chr2:96781269 | G | A | 5 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-15743G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781269 | |||||||
| chr2:96781356 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1403-15656A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781356 | |||||||
| chr2:96781384 | C | G | 30 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1403-15628C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781384 | |||||||
| chr2:96781566 | C | A | 2 | a0001c0001t0001g0251 a0003c0006t0001g0253 |
2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1403-15446C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96781566 | |||||||
| chr2:96782094 | T | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(152): Show |
157 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.1403-14918T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782094 | |||||||
| chr2:96782318 | G | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14694G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782318 | |||||||
| chr2:96782336 | T | C | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14676T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782336 | |||||||
| chr2:96782390 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(56): Show |
60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-14622C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782390 | |||||||
| chr2:96782411 | C | CA | 29 | a0001c0001t0001g0017 a0001c0001t0001g0058 a0001c0001t0001g0168 others(26): Show |
29 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1403-14585dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96782411 | ||||||
| chr2:96782545 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
5 | HG03225.hp2 NA18522.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-14467G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782545 | |||||||
| chr2:96782640 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14372A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782640 | |||||||
| chr2:96782737 | G | T | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-14275G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782737 | |||||||
| chr2:96782864 | G | A | 2 | a0001c0001t0002g0220 a0001c0001t0002g0235 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1403-14148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782864 | |||||||
| chr2:96782871 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1403-14141G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96782871 | |||||||
| chr2:96783197 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1403-13815C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96783197 | |||||||
| chr2:96783438 | C | T | 1 | a0001c0001t0006g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1403-13574C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96783438 | |||||||
| chr2:96783785 | A | G | 5 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-13227A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96783785 | |||||||
| chr2:96784025 | A | C | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-12987A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784025 | |||||||
| chr2:96784597 | T | G | 3 | a0001c0001t0004g0116 a0001c0001t0004g0117 a0001c0001t0004g0119 |
3 | HG02486.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1403-12415T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784597 | |||||||
| chr2:96784615 | C | G | 3 | a0001c0001t0005g0092 a0001c0001t0006g0076 a0001c0001t0006g0077 |
3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1403-12397C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784615 | |||||||
| chr2:96784772 | T | C | 28 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0116 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1403-12240T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96784772 | |||||||
| chr2:96785227 | A | G | 2 | a0001c0001t0004g0128 a0001c0001t0004g0136 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1403-11785A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785227 | |||||||
| chr2:96785237 | CT | C | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-11766delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96785237 | ||||||
| chr2:96785630 | T | C | 1 | a0001c0001t0004g0122 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1403-11382T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785630 | |||||||
| chr2:96785663 | G | T | 1 | a0001c0001t0006g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1403-11349G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785663 | |||||||
| chr2:96785708 | G | A | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1403-11304G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96785708 | |||||||
| chr2:96786255 | A | G | 2 | a0001c0001t0003g0104 a0001c0001t0013g0106 |
2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1403-10757A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786255 | |||||||
| chr2:96786363 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-10649A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786363 | |||||||
| chr2:96786374 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1403-10638A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786374 | |||||||
| chr2:96786413 | C | CA | 36 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0170 others(33): Show |
37 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1403-10584dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786413 | ||||||
| chr2:96786413 | CA | C | 17 | a0001c0001t0001g0058 a0001c0001t0001g0167 a0001c0001t0001g0230 others(14): Show |
17 | HG00323.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1403-10584delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786413 | ||||||
| chr2:96786507 | G | A | 3 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0088 |
3 | HG01099.hp1 HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1403-10505G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786507 | |||||||
| chr2:96786679 | C | T | 8 | a0001c0001t0002g0062 a0001c0001t0002g0064 a0001c0001t0002g0067 others(5): Show |
8 | HG00609.hp1 HG02056.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1403-10333C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96786679 | |||||||
| chr2:96786778 | C | CA | 23 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0196 others(20): Show |
24 | HG00741.hp1 HG01106.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1403-10208dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786778 | ||||||
| chr2:96786778 | CA | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(74): Show |
78 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1403-10208delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96786778 | ||||||
| chr2:96787003 | T | C | 1 | a0001c0001t0004g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1403-10009T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787003 | |||||||
| chr2:96787100 | A | G | 2 | a0001c0001t0002g0220 a0001c0001t0002g0235 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1403-9912A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787100 | |||||||
| chr2:96787248 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1403-9764A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787248 | |||||||
| chr2:96787579 | C | T | 3 | a0001c0001t0005g0092 a0001c0001t0006g0076 a0001c0001t0006g0077 |
3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1403-9433C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787579 | |||||||
| chr2:96787659 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1403-9353A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96787659 | |||||||
| chr2:96788166 | G | T | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1403-8846G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788166 | |||||||
| chr2:96788252 | C | CT | 11 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0246 others(8): Show |
11 | HG02071.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1403-8743dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96788252 | ||||||
| chr2:96788386 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00423.hp2 NA18612.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-8626C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788386 | |||||||
| chr2:96788718 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-8294C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788718 | |||||||
| chr2:96788818 | CCTT | C | 5 | a0001c0001t0003g0095 a0001c0001t0003g0097 a0001c0001t0003g0103 others(2): Show |
5 | NA18950.hp2 NA19054.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403-8190_1403-818 others(7): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96788818 | ||||||
| chr2:96788913 | T | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-8099T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788913 | |||||||
| chr2:96788968 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-8044C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96788968 | |||||||
| chr2:96788984 | CT | C | 59 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(56): Show |
60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-8021delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96788984 | ||||||
| chr2:96789333 | G | A | 1 | a0001c0001t0003g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1403-7679G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789333 | |||||||
| chr2:96789452 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1403-7560C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789452 | |||||||
| chr2:96789479 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 |
4 | HG00642.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1403-7533C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789479 | |||||||
| chr2:96789539 | G | A | 2 | a0001c0003t0001g0248 a0001c0003t0001g0260 |
2 | HG01081.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1403-7473G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789539 | |||||||
| chr2:96789574 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-7438C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789574 | |||||||
| chr2:96789700 | A | AT | 7 | a0001c0001t0003g0075 a0001c0001t0003g0102 a0001c0001t0003g0109 others(4): Show |
7 | HG01891.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-7298dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96789700 | ||||||
| chr2:96789841 | C | T | 1 | a0001c0001t0008g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1403-7171C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789841 | |||||||
| chr2:96789877 | G | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02071.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1403-7135G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789877 | |||||||
| chr2:96789881 | C | T | 13 | a0001c0001t0003g0004 a0001c0001t0003g0094 a0001c0001t0003g0095 others(10): Show |
14 | HG01981.hp2 HG02155.hp2 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1403-7131C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789881 | |||||||
| chr2:96789913 | G | C | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1403-7099G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789913 | |||||||
| chr2:96789978 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(46): Show |
50 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1403-7034C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96789978 | |||||||
| chr2:96790003 | A | AT | 30 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0162 others(27): Show |
30 | HG00639.hp2 HG00673.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1403-6986dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96790003 | ||||||
| chr2:96790003 | AT | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0047 others(6): Show |
9 | HG00558.hp1 HG01256.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1403-6986delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96790003 | ||||||
| chr2:96790031 | C | T | 1 | a0001c0001t0004g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1403-6981C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790031 | |||||||
| chr2:96790250 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1403-6762C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790250 | |||||||
| chr2:96790285 | C | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1403-6727C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790285 | |||||||
| chr2:96790290 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02071.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1403-6722G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790290 | |||||||
| chr2:96790297 | C | T | 12 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(9): Show |
12 | HG01261.hp2 HG01358.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1403-6715C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790297 | |||||||
| chr2:96790423 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1403-6589C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790423 | |||||||
| chr2:96790500 | A | G | 2 | a0001c0001t0003g0084 a0001c0001t0003g0088 |
2 | HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1403-6512A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790500 | |||||||
| chr2:96790675 | C | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0058 |
3 | HG00544.hp2 NA19000.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1403-6337C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790675 | |||||||
| chr2:96790749 | G | A | 1 | a0001c0001t0006g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1403-6263G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790749 | |||||||
| chr2:96790841 | T | C | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-6171T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96790841 | |||||||
| chr2:96791013 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1403-5999G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791013 | |||||||
| chr2:96791119 | C | CA | 7 | a0001c0001t0001g0045 a0001c0001t0001g0170 a0001c0001t0001g0174 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-5874dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791119 | ||||||
| chr2:96791119 | CA | C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
17 | HG00558.hp1 HG00642.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1403-5874delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791119 | ||||||
| chr2:96791277 | G | T | 9 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1403-5735G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791277 | |||||||
| chr2:96791305 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1403-5707A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791305 | |||||||
| chr2:96791382 | G | A | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-5630G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791382 | |||||||
| chr2:96791483 | AT | A | 3 | a0001c0001t0005g0092 a0001c0001t0006g0076 a0001c0001t0006g0077 |
3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1403-5527delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791483 | ||||||
| chr2:96791505 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1403-5507C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791505 | |||||||
| chr2:96791550 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1403-5462C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791550 | |||||||
| chr2:96791588 | C | CA | 15 | a0001c0001t0001g0040 a0001c0001t0001g0208 a0001c0001t0001g0236 others(12): Show |
15 | HG00639.hp1 HG02055.hp1 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.1403-5410dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96791588 | ||||||
| chr2:96791652 | T | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-5360T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96791652 | |||||||
| chr2:96792019 | C | T | 11 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(8): Show |
11 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1403-4993C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792019 | |||||||
| chr2:96792112 | G | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-4900G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792112 | |||||||
| chr2:96792208 | T | G | 1 | a0001c0001t0007g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1403-4804T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792208 | |||||||
| chr2:96792245 | C | CA | 30 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0058 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1403-4751dupA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96792245 | ||||||
| chr2:96792307 | G | A | 3 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0006g0078 |
3 | HG00642.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1403-4705G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792307 | |||||||
| chr2:96792416 | C | A | 1 | a0001c0001t0001g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1403-4596C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792416 | |||||||
| chr2:96792448 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1403-4564G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792448 | |||||||
| chr2:96792668 | G | A | 3 | a0001c0001t0004g0121 a0001c0001t0004g0126 a0001c0001t0004g0127 |
3 | HG01891.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1403-4344G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792668 | |||||||
| chr2:96792699 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-4313C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792699 | |||||||
| chr2:96792794 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1403-4218C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792794 | |||||||
| chr2:96792824 | A | G | 67 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(64): Show |
68 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1403-4188A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792824 | |||||||
| chr2:96792855 | G | C | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1403-4157G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96792855 | |||||||
| chr2:96793666 | A | T | 32 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403-3346A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793666 | |||||||
| chr2:96793793 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(56): Show |
60 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1403-3219G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793793 | |||||||
| chr2:96793870 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1403-3142G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793870 | |||||||
| chr2:96793905 | A | G | 30 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1403-3107A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96793905 | |||||||
| chr2:96794183 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1403-2829A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794183 | |||||||
| chr2:96794388 | C | T | 1 | a0001c0001t0007g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1403-2624C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794388 | |||||||
| chr2:96794677 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(5): Show |
8 | HG00544.hp2 HG02523.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1403-2335G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794677 | |||||||
| chr2:96794758 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1403-2254A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794758 | |||||||
| chr2:96794857 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0055 |
2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1403-2155A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794857 | |||||||
| chr2:96794910 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0222 |
2 | HG00609.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1403-2102G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96794910 | |||||||
| chr2:96795037 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0069 |
2 | HG00609.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1403-1975G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795037 | |||||||
| chr2:96795288 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1403-1724C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795288 | |||||||
| chr2:96795357 | G | A | 1 | a0001c0002t0005g0074 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1403-1655G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795357 | |||||||
| chr2:96795487 | A | AC | 21 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0054 others(18): Show |
21 | HG00423.hp1 HG00733.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1403-1514dupC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96795487 | ||||||
| chr2:96795487 | AC | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0147 others(103): Show |
108 | HG00558.hp2 HG01070.hp1 HG01070.hp2 others(105): Show |
intron_variant | MODIFIER | c.1403-1514delC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96795487 | ||||||
| chr2:96795493 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1403-1519C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795493 | |||||||
| chr2:96795933 | C | T | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-1079C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96795933 | |||||||
| chr2:96796131 | C | CT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
77 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1403-850dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | C | CTT | 21 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0043 others(18): Show |
21 | HG01175.hp1 HG02080.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1403-851_1403-850d others(4): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | CT | C | 26 | a0001c0001t0001g0091 a0001c0001t0001g0185 a0001c0001t0001g0211 others(23): Show |
26 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.1403-850delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | CTT | C | 25 | a0001c0001t0003g0004 a0001c0001t0003g0081 a0001c0001t0003g0082 others(22): Show |
26 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1403-851_1403-850d others(4): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | CTTT | C | 5 | a0001c0001t0003g0075 a0001c0001t0003g0085 a0001c0001t0003g0096 others(2): Show |
5 | HG01168.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-852_1403-850d others(5): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0193 a0001c0001t0004g0121 a0001c0001t0004g0126 others(12): Show |
15 | HG00423.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1403-861_1403-850d others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG02965.hp2 HG04204.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403-862_1403-850d others(15): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796131 | CTTTTTTT others(7): Show |
C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0030 a0001c0001t0002g0056 others(4): Show |
7 | NA18949.hp2 NA18951.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1403-863_1403-850d others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 96796131 | ||||||
| chr2:96796214 | G | A | 5 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0188 others(2): Show |
5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1403-798G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796214 | |||||||
| chr2:96796269 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1403-743C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796269 | |||||||
| chr2:96796344 | C | T | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1403-668C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796344 | |||||||
| chr2:96796491 | G | A | 27 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0121 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1403-521G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796491 | |||||||
| chr2:96796633 | C | T | 1 | a0001c0001t0006g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1403-379C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 1/6 | chr2 | 96796633 | |||||||
| chr2:96797291 | C | G | 5 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546+136C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797291 | |||||||
| chr2:96797333 | C | T | 6 | a0001c0001t0001g0167 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG00323.hp1 HG00733.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546+178C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797333 | |||||||
| chr2:96797358 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(151): Show |
156 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1547-155T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797358 | |||||||
| chr2:96797441 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1547-72C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 2/6 | chr2 | 96797441 | |||||||
| chr2:96797691 | C | T | 1 | a0001c0001t0003g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1681+44C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797691 | |||||||
| chr2:96797718 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1681+71G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797718 | |||||||
| chr2:96797791 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1681+144C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797791 | |||||||
| chr2:96797792 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(149): Show |
154 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1681+145G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797792 | |||||||
| chr2:96797846 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(5): Show |
9 | HG00642.hp2 HG00741.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1681+199C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797846 | |||||||
| chr2:96797848 | G | A | 3 | a0001c0001t0005g0092 a0001c0001t0006g0076 a0001c0001t0006g0077 |
3 | HG01891.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1681+201G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96797848 | |||||||
| chr2:96798095 | G | T | 1 | a0001c0001t0003g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1681+448G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798095 | |||||||
| chr2:96798320 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1681+673C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798320 | |||||||
| chr2:96798540 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1682-517C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798540 | |||||||
| chr2:96798689 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1682-368C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798689 | |||||||
| chr2:96798831 | A | G | 2 | a0001c0001t0003g0096 a0001c0001t0003g0111 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1682-226A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798831 | |||||||
| chr2:96798909 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1682-148G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96798909 | |||||||
| chr2:96799041 | C | T | 1 | a0001c0001t0006g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1682-16C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 3/6 | chr2 | 96799041 | |||||||
| chr2:96799285 | A | G | 1 | a0001c0001t0006g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1851+59A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 4/6 | chr2 | 96799285 | |||||||
| chr2:96799327 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1851+101G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 4/6 | chr2 | 96799327 | |||||||
| chr2:96799954 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1948+306A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96799954 | |||||||
| chr2:96799988 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1948+340C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96799988 | |||||||
| chr2:96800097 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1948+449G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96800097 | |||||||
| chr2:96800592 | G | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0222 |
2 | HG00609.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1948+944G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96800592 | |||||||
| chr2:96800873 | GC | G | 33 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0115 others(30): Show |
33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1948+1227delC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96800873 | ||||||
| chr2:96801001 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1948+1353C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801001 | |||||||
| chr2:96801246 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1948+1598G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801246 | |||||||
| chr2:96801507 | G | GAGAGACC others(42): Show |
1 | a0001c0001t0001g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1948+1908_1948+195 others(53): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801507 | ||||||
| chr2:96801509 | G | T | 5 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0188 others(2): Show |
5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1861G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801509 | |||||||
| chr2:96801512 | A | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0188 others(2): Show |
5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1864A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801512 | |||||||
| chr2:96801513 | C | A | 5 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0188 others(2): Show |
5 | HG01070.hp1 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1865C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801513 | |||||||
| chr2:96801527 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0069 |
2 | HG00609.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1948+1879A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801527 | |||||||
| chr2:96801537 | CAG | C | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1948+1895_1948+189 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801537 | ||||||
| chr2:96801585 | ACAGAGAG others(55): Show |
A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1948+1957_1948+201 others(66): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801585 | ||||||
| chr2:96801596 | ACACACAC others(6): Show |
A | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1948+1967_1948+197 others(17): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801596 | ||||||
| chr2:96801600 | ACACAGAG others(49): Show |
A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1948+1957_1948+201 others(60): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801600 | ||||||
| chr2:96801656 | C | CCA | 6 | a0001c0001t0001g0034 a0001c0001t0002g0016 a0001c0001t0002g0030 others(3): Show |
6 | NA18949.hp2 NA18951.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.1948+2025_1948+202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801656 | ||||||
| chr2:96801656 | C | CCACACA | 3 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 |
3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1948+2021_1948+202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801656 | ||||||
| chr2:96801673 | C | G | 2 | a0001c0001t0006g0076 a0001c0001t0006g0077 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1948+2025C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801673 | |||||||
| chr2:96801724 | C | CAG | 29 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(26): Show |
30 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1948+2080_1948+208 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96801724 | ||||||
| chr2:96801729 | A | AGACC | 36 | a0001c0001t0002g0217 a0001c0001t0004g0079 a0001c0001t0004g0080 others(33): Show |
36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1948+2081_1948+208 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801729 | |||||||
| chr2:96801730 | C | A | 36 | a0001c0001t0002g0217 a0001c0001t0004g0079 a0001c0001t0004g0080 others(33): Show |
36 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1948+2082C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801730 | |||||||
| chr2:96801752 | C | A | 9 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1948+2104C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801752 | |||||||
| chr2:96801780 | C | G | 10 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1948+2132C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801780 | |||||||
| chr2:96801803 | T | G | 33 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0115 others(30): Show |
33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1948+2155T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801803 | |||||||
| chr2:96801832 | C | T | 1 | a0001c0001t0003g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1948+2184C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801832 | |||||||
| chr2:96801917 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1948+2269C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96801917 | |||||||
| chr2:96802002 | GAC | G | 5 | a0001c0001t0006g0078 a0001c0001t0006g0232 a0001c0001t0006g0233 others(2): Show |
5 | HG00642.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1948+2368_1948+236 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96802002 | ||||||
| chr2:96802173 | C | T | 33 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0115 others(30): Show |
33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1948+2525C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96802173 | |||||||
| chr2:96802445 | C | T | 1 | a0001c0001t0008g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1948+2797C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96802445 | |||||||
| chr2:96802539 | G | C | 65 | a0001c0001t0002g0217 a0001c0001t0003g0004 a0001c0001t0003g0075 others(62): Show |
66 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.1948+2891G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96802539 | |||||||
| chr2:96803012 | G | T | 1 | a0001c0001t0003g0103 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1948+3364G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803012 | |||||||
| chr2:96803339 | T | G | 1 | a0001c0001t0003g0088 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1948+3691T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803339 | |||||||
| chr2:96803453 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1948+3805G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803453 | |||||||
| chr2:96803641 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0002g0217 |
2 | HG03453.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1948+3993G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803641 | |||||||
| chr2:96803725 | TA | T | 115 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0002g0006 others(112): Show |
116 | HG00609.hp1 HG00642.hp1 HG01070.hp2 others(113): Show |
intron_variant | MODIFIER | c.1948+4090delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96803725 | ||||||
| chr2:96803739 | C | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0055 |
2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1948+4091C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803739 | |||||||
| chr2:96803881 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1948+4233T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803881 | |||||||
| chr2:96803897 | T | C | 10 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1948+4249T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96803897 | |||||||
| chr2:96804074 | T | A | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1948+4426T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804074 | |||||||
| chr2:96804226 | A | AT | 5 | a0001c0001t0001g0168 a0001c0001t0001g0200 a0001c0001t0001g0216 others(2): Show |
5 | HG00639.hp2 HG02886.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949-4314dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96804226 | ||||||
| chr2:96804226 | AT | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0158 others(15): Show |
18 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1949-4314delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96804226 | ||||||
| chr2:96804486 | C | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0075 a0001c0001t0003g0081 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1949-4075C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804486 | |||||||
| chr2:96804561 | T | C | 1 | a0001c0001t0003g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1949-4000T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804561 | |||||||
| chr2:96804637 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0181 |
2 | NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1949-3924G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804637 | |||||||
| chr2:96804778 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0189 |
2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1949-3783C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804778 | |||||||
| chr2:96804782 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1949-3779C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96804782 | |||||||
| chr2:96805170 | G | A | 33 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0115 others(30): Show |
33 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1949-3391G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805170 | |||||||
| chr2:96805284 | ACTATAAA others(32): Show |
A | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1949-3273_1949-323 others(43): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805284 | ||||||
| chr2:96805418 | G | GT | 76 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0071 others(73): Show |
76 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1949-3122dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | ||||||
| chr2:96805418 | G | GTT | 41 | a0001c0001t0001g0194 a0001c0001t0001g0203 a0001c0001t0002g0006 others(38): Show |
41 | HG00609.hp1 HG00642.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1949-3123_1949-312 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | ||||||
| chr2:96805418 | G | GTTT | 27 | a0001c0001t0002g0057 a0001c0001t0002g0150 a0001c0001t0003g0004 others(24): Show |
28 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1949-3124_1949-312 others(7): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | ||||||
| chr2:96805418 | GT | G | 10 | a0001c0001t0001g0046 a0001c0001t0001g0180 a0001c0001t0001g0250 others(7): Show |
10 | HG00280.hp2 HG01517.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-3122delT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96805418 | ||||||
| chr2:96805426 | T | A | 3 | a0001c0001t0007g0165 a0001c0001t0007g0166 a0001c0009t0007g0191 |
3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1949-3135T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805426 | |||||||
| chr2:96805432 | T | A | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-3129T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805432 | |||||||
| chr2:96805433 | T | A | 3 | a0001c0001t0007g0165 a0001c0001t0007g0166 a0001c0009t0007g0191 |
3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1949-3128T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805433 | |||||||
| chr2:96805437 | T | A | 15 | a0001c0001t0004g0121 a0001c0001t0004g0149 a0001c0001t0005g0092 others(12): Show |
15 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1949-3124T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805437 | |||||||
| chr2:96805437 | T | TA | 7 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1949-3124_1949-312 others(5): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805437 | |||||||
| chr2:96805438 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1949-3123T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805438 | |||||||
| chr2:96805439 | TA | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0037 others(6): Show |
9 | HG00323.hp2 HG00558.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1949-3121delA | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805439 | |||||||
| chr2:96805440 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
51 | HG00280.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1949-3121A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805440 | |||||||
| chr2:96805443 | A | T | 3 | a0001c0001t0001g0066 a0001c0001t0007g0164 a0001c0001t0012g0114 |
3 | HG02055.hp1 HG02056.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1949-3118A>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805443 | |||||||
| chr2:96805445 | T | A | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1949-3116T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805445 | |||||||
| chr2:96805445 | T | TA | 29 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0115 others(26): Show |
29 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1949-3116_1949-311 others(5): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805445 | |||||||
| chr2:96805454 | A | C | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-3107A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805454 | |||||||
| chr2:96805500 | T | G | 1 | a0001c0001t0005g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1949-3061T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805500 | |||||||
| chr2:96805637 | T | G | 2 | a0001c0001t0004g0079 a0001c0001t0004g0080 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1949-2924T>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805637 | |||||||
| chr2:96805644 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1949-2917T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805644 | |||||||
| chr2:96805657 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1949-2904G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96805657 | |||||||
| chr2:96806025 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1949-2536C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806025 | |||||||
| chr2:96806043 | ACCTCCCG others(94): Show |
A | 10 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-2490_1949-239 others(4): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806043 | ||||||
| chr2:96806053 | C | A | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-2508C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806053 | |||||||
| chr2:96806080 | G | A | 12 | a0001c0001t0003g0004 a0001c0001t0003g0094 a0001c0001t0003g0095 others(9): Show |
13 | HG01981.hp2 HG02155.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1949-2481G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806080 | |||||||
| chr2:96806081 | A | AC | 22 | a0001c0001t0002g0157 a0001c0001t0004g0115 a0001c0001t0004g0116 others(19): Show |
22 | HG01261.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1949-2472dupC | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806081 | ||||||
| chr2:96806090 | A | C | 23 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1949-2471A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806090 | |||||||
| chr2:96806105 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1949-2456G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806105 | |||||||
| chr2:96806105 | GGGGGCGG others(42): Show |
G | 1 | a0001c0001t0001g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1949-2427_1949-237 others(53): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806105 | ||||||
| chr2:96806126 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1949-2435G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806126 | |||||||
| chr2:96806143 | G | T | 23 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1949-2418G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806143 | |||||||
| chr2:96806154 | C | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0227 a0001c0001t0001g0229 |
3 | HG01361.hp1 HG01934.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1949-2407C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806154 | |||||||
| chr2:96806317 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1949-2244A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806317 | |||||||
| chr2:96806426 | C | T | 79 | a0001c0001t0001g0023 a0001c0001t0001g0090 a0001c0001t0001g0091 others(76): Show |
79 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1949-2135C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806426 | |||||||
| chr2:96806506 | A | AAC | 26 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0027 others(23): Show |
26 | HG00609.hp1 HG00673.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1949-2026_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | A | AACAC | 23 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0043 others(20): Show |
23 | HG00558.hp1 HG01884.hp2 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.1949-2028_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | A | AACACAC | 5 | a0001c0001t0002g0006 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1949-2030_1949-202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | A | AACACACA others(3): Show |
1 | a0001c0001t0002g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1949-2034_1949-202 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | A | AACACACA others(7): Show |
1 | a0001c0001t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1949-2038_1949-202 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | A | AACACACA others(9): Show |
2 | a0001c0001t0002g0143 a0001c0001t0002g0156 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1949-2040_1949-202 others(20): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | AAC | A | 8 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0173 others(5): Show |
8 | HG01168.hp2 HG02109.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-2026_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806506 | AACAC | A | 3 | a0001c0001t0006g0076 a0001c0001t0006g0077 a0001c0001t0008g0237 |
3 | HG01891.hp2 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1949-2028_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806506 | ||||||
| chr2:96806528 | C | A | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1949-2033C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806528 | |||||||
| chr2:96806529 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0008g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1949-2030_1949-201 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806529 | ||||||
| chr2:96806529 | ACACACAC others(13): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1949-2030_1949-201 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806529 | ||||||
| chr2:96806531 | A | ACG | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0251 |
3 | HG00280.hp2 HG00423.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1949-2029_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806531 | ||||||
| chr2:96806531 | A | G | 1 | a0001c0001t0008g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1949-2030A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806531 | |||||||
| chr2:96806533 | A | ACG | 12 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0159 others(9): Show |
12 | HG00544.hp2 HG00639.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.1949-2027_1949-202 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806533 | ||||||
| chr2:96806533 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0182 a0001c0001t0001g0209 others(6): Show |
9 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.1949-2028A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806533 | |||||||
| chr2:96806533 | ACACG | A | 6 | a0001c0001t0006g0078 a0001c0001t0006g0186 a0001c0001t0006g0232 others(3): Show |
6 | HG00642.hp1 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1949-2026_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806533 | ||||||
| chr2:96806535 | A | ACACACAC others(13): Show |
1 | a0001c0001t0002g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(24): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACACAC others(9): Show |
3 | a0001c0001t0002g0145 a0001c0001t0002g0152 a0001c0001t0002g0157 |
3 | HG01261.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(20): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACACAC others(11): Show |
1 | a0001c0001t0002g0144 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(22): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACACAC others(7): Show |
2 | a0001c0001t0002g0151 a0001c0001t0002g0154 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(18): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACACG | 7 | a0001c0001t0001g0002 a0001c0001t0002g0007 a0001c0001t0003g0075 others(4): Show |
7 | HG01256.hp2 HG01993.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACACGC others(1): Show |
5 | a0001c0001t0003g0004 a0001c0001t0003g0083 a0001c0001t0003g0084 others(2): Show |
5 | HG01099.hp1 HG01261.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(12): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACACGC others(5): Show |
1 | a0001c0001t0003g0004 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACG | 15 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0018 others(12): Show |
15 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(8): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACGCG | 8 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0195 others(5): Show |
8 | HG00642.hp2 HG01169.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(10): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACGCGC others(1): Show |
3 | a0001c0001t0003g0097 a0001c0001t0003g0105 a0001c0001t0013g0106 |
3 | NA19054.hp1 NA19064.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1949-2025_1949-202 others(12): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACGCGC others(3): Show |
1 | a0001c0001t0003g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACACGCGC others(5): Show |
1 | a0001c0001t0003g0112 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1949-2025_1949-202 others(16): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | ACG | 22 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0026 others(19): Show |
22 | HG00544.hp1 HG01255.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1949-2008_1949-200 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0038 others(28): Show |
31 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1949-2026A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806535 | |||||||
| chr2:96806535 | ACG | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0057 a0001c0001t0002g0062 others(1): Show |
4 | HG02717.hp2 HG06807.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949-2008_1949-200 others(6): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806535 | ACGCGCGC others(3): Show |
A | 1 | a0001c0001t0007g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1949-2016_1949-200 others(14): Show |
CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 96806535 | ||||||
| chr2:96806537 | G | A | 47 | a0001c0001t0001g0052 a0001c0001t0001g0203 a0001c0001t0002g0008 others(44): Show |
47 | HG00609.hp1 HG00673.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.1949-2024G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806537 | |||||||
| chr2:96806539 | G | A | 24 | a0001c0001t0002g0062 a0001c0001t0002g0113 a0001c0001t0002g0153 others(21): Show |
24 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1949-2022G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806539 | |||||||
| chr2:96806541 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0002g0113 |
2 | HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1949-2020G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806541 | |||||||
| chr2:96806546 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0015g0240 |
2 | HG00099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1949-2015C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806546 | |||||||
| chr2:96806873 | C | G | 1 | a0001c0001t0012g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1949-1688C>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806873 | |||||||
| chr2:96806993 | T | A | 1 | a0001c0001t0006g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1949-1568T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96806993 | |||||||
| chr2:96807068 | T | C | 6 | a0001c0001t0004g0115 a0001c0001t0004g0116 a0001c0001t0004g0117 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1949-1493T>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807068 | |||||||
| chr2:96807096 | C | T | 1 | a0001c0001t0004g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1949-1465C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807096 | |||||||
| chr2:96807261 | G | A | 11 | a0001c0001t0005g0124 a0001c0001t0005g0141 a0001c0002t0005g0074 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1949-1300G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807261 | |||||||
| chr2:96807286 | G | A | 10 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0122 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-1275G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807286 | |||||||
| chr2:96807381 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1949-1180G>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807381 | |||||||
| chr2:96807559 | C | A | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1949-1002C>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807559 | |||||||
| chr2:96807751 | C | T | 1 | a0001c0001t0008g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1949-810C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807751 | |||||||
| chr2:96807752 | G | A | 8 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0128 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-809G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807752 | |||||||
| chr2:96807872 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1949-689A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96807872 | |||||||
| chr2:96808029 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1949-532C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96808029 | |||||||
| chr2:96808074 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1949-487A>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96808074 | |||||||
| chr2:96808192 | A | G | 113 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(110): Show |
114 | HG00609.hp1 HG00642.hp1 HG01070.hp2 others(111): Show |
intron_variant | MODIFIER | c.1949-369A>G | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 5/6 | chr2 | 96808192 | |||||||
| chr2:96808789 | G | C | 1 | a0001c0002t0005g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2130+47G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96808789 | |||||||
| chr2:96808840 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2130+98G>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96808840 | |||||||
| chr2:96809002 | G | GT | 35 | a0001c0001t0001g0060 a0001c0001t0002g0057 a0001c0001t0002g0067 others(32): Show |
35 | HG01884.hp1 HG01884.hp2 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.2130+274dupT | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 96809002 | ||||||
| chr2:96809088 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2131-232C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809088 | |||||||
| chr2:96809102 | G | C | 1 | a0001c0001t0001g0025 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2131-218G>C | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809102 | |||||||
| chr2:96809143 | T | A | 8 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0128 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2131-177T>A | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809143 | |||||||
| chr2:96809150 | C | T | 1 | a0001c0001t0003g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2131-170C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809150 | |||||||
| chr2:96809165 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2131-155C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809165 | |||||||
| chr2:96809199 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2131-121C>T | CNNM4 | ENSG00000158158.12 | transcript | ENST00000377075.3 | protein_coding | 6/6 | chr2 | 96809199 |