Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22908 |
| ensemblid | ENSG00000211456.14 |
| hgncid | 17059 |
| symbol | SACM1L |
| name | SAC1 like phosphatidylinositide phosphatase |
| refseq_nuc | NM_014016.5 |
| refseq_prot | NP_054735.3 |
| ensembl_nuc | ENST00000389061.10 |
| ensembl_prot | ENSP00000373713.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 45689396 |
| end | 45745409 |
| strand | + |
| ver | v1.2 |
| region | chr3:45689396-45745409 |
| region5000 | chr3:45684396-45750409 |
| regionname0 | SACM1L_chr3_45689396_45745409 |
| regionname5000 | SACM1L_chr3_45684396_45750409 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 587 | 198 | 54 | 46 | 72 | 10 | 15 | 54 | SACM1L_chr3_45684396_45750409 | SACM1L | MATAA others(582): Show |
chr3 | 45684396 | 45750409 |
| a0002 | 1/0 | 587 | 155 | 28 | 23 | 82 | 6 | 15 | 62 | SACM1L_chr3_45684396_45750409 | SACM1L | MATAA others(582): Show |
chr3 | 45684396 | 45750409 |
| a0003 | 0/0 | 587 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | MATAA others(582): Show |
chr3 | 45684396 | 45750409 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1761 | 141 | 35 | 31 | 53 | 10 | 11 | SACM1L_chr3_45684396_45750409 | SACM1L | ATGGC others(1756): Show |
chr3 | 45684396 | 45750409 | ||
| a0001c0003 | 0/0 | 1761 | 54 | 17 | 15 | 18 | 0 | 4 | SACM1L_chr3_45684396_45750409 | SACM1L | ATGGC others(1756): Show |
chr3 | 45684396 | 45750409 | ||
| a0001c0004 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | ATGGC others(1756): Show |
chr3 | 45684396 | 45750409 | ||
| a0001c0006 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | ATGGC others(1756): Show |
chr3 | 45684396 | 45750409 | ||
| a0002c0001 | 1/0 | 1761 | 155 | 28 | 23 | 82 | 6 | 15 | SACM1L_chr3_45684396_45750409 | SACM1L | ATGGC others(1756): Show |
chr3 | 45684396 | 45750409 | ||
| a0003c0005 | 0/0 | 1761 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | ATGGC others(1756): Show |
chr3 | 45684396 | 45750409 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 3575 | 70 | 17 | 26 | 13 | 6 | 8 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0003 | 0/0 | 3570 | 23 | 0 | 0 | 22 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3565): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0004 | 0/0 | 3575 | 19 | 16 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0005 | 0/0 | 3575 | 17 | 0 | 0 | 14 | 1 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0006 | 0/1 | 3575 | 4 | 0 | 1 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0007 | 0/0 | 3575 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0011 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0012 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0002t0013 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0003t0002 | 0/0 | 3575 | 53 | 16 | 15 | 18 | 0 | 4 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0003t0015 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0004t0002 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0001c0006t0002 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| a0002c0001t0001 | 1/0 | 3574 | 147 | 26 | 19 | 80 | 6 | 15 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3569): Show |
chr3 | 45684396 | 45750409 |
| a0002c0001t0008 | 0/0 | 3574 | 3 | 0 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3569): Show |
chr3 | 45684396 | 45750409 |
| a0002c0001t0009 | 0/0 | 3574 | 2 | 1 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3569): Show |
chr3 | 45684396 | 45750409 |
| a0002c0001t0010 | 0/0 | 3574 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3569): Show |
chr3 | 45684396 | 45750409 |
| a0002c0001t0014 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3569): Show |
chr3 | 45684396 | 45750409 |
| a0003c0005t0002 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | AGAGT others(3570): Show |
chr3 | 45684396 | 45750409 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0009 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0010 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0015 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0006g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0006g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0011g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0012g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0002t0013g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0003 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0003t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0004t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0001c0006t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0001 | 0/0 | 19 | 2 | 1 | 12 | 2 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0005 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0008g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0009g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0010g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0002c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| a0003c0005t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0019 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0127 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00140 | hp2 | a0001 | c0002 | t0006 | g0017 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | FIN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00323 | hp2 | a0001 | c0002 | t0006 | g0017 | EUR | FIN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0216 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0233 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0189 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00597 | hp2 | a0001 | c0002 | t0007 | g0021 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0154 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00609 | hp2 | a0002 | c0001 | t0010 | g0025 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0099 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0212 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0181 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0213 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0180 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0148 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0026 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0193 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0125 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0184 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0043 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0052 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0090 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0206 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0108 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0028 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0086 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0080 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0045 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01243 | hp1 | a0002 | c0001 | t0009 | g0103 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0067 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0100 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01257 | hp1 | a0001 | c0002 | t0013 | g0017 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01257 | hp2 | a0002 | c0001 | t0008 | g0185 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01258 | hp1 | a0002 | c0001 | t0008 | g0202 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0237 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01358 | hp1 | a0002 | c0001 | t0008 | g0045 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0007 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0075 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0028 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0093 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01515 | hp2 | a0001 | c0002 | t0012 | g0120 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0036 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0027 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0027 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0023 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0097 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0117 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0241 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01934 | hp2 | a0003 | c0005 | t0002 | g0014 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01943 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0124 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0232 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0007 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0089 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0060 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0082 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02056 | hp1 | a0001 | c0002 | t0005 | g0169 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0228 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0218 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0092 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02129 | hp1 | a0002 | c0001 | t0010 | g0025 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02132 | hp1 | a0001 | c0002 | t0005 | g0147 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02145 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0182 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02155 | hp1 | a0002 | c0001 | t0001 | g0194 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02155 | hp2 | a0001 | c0002 | t0005 | g0037 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0145 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0041 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0210 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0175 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0031 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02451 | hp2 | a0002 | c0001 | t0001 | g0106 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0227 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0081 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0141 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0220 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0140 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0023 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0033 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0046 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0042 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0050 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02735 | hp2 | a0001 | c0002 | t0005 | g0146 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0118 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0040 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02886 | hp1 | a0001 | c0002 | t0011 | g0049 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0096 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0039 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0059 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0172 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02897 | hp2 | a0002 | c0001 | t0001 | g0058 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02965 | hp2 | a0001 | c0003 | t0015 | g0053 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0171 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0005 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0024 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0095 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0078 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0139 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0173 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0031 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0102 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0142 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0042 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03139 | hp2 | a0001 | c0002 | t0011 | g0049 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0098 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0022 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03209 | hp1 | a0002 | c0001 | t0001 | g0030 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03209 | hp2 | a0002 | c0001 | t0009 | g0104 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0061 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0039 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03453 | hp1 | a0002 | c0001 | t0001 | g0057 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0062 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0056 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0085 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0033 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03516 | hp2 | a0002 | c0001 | t0001 | g0105 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0136 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0176 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0143 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0219 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0222 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0019 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0019 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0043 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0195 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0131 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03831 | hp1 | a0001 | c0002 | t0005 | g0163 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0221 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0238 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0231 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0026 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0248 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0107 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0040 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0250 | EAS | CHB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0187 | EAS | CHB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0024 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0046 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18952 | hp2 | a0001 | c0002 | t0005 | g0138 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18953 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18956 | hp1 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18957 | hp1 | a0001 | c0002 | t0005 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0196 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18960 | hp1 | a0001 | c0002 | t0005 | g0170 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18962 | hp2 | a0001 | c0002 | t0005 | g0037 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0226 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18964 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18967 | hp1 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18977 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0191 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0192 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0204 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18987 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18987 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18988 | hp1 | a0001 | c0003 | t0002 | g0087 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18989 | hp1 | a0001 | c0002 | t0005 | g0164 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18991 | hp2 | a0002 | c0001 | t0001 | g0065 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18992 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18992 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0159 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0199 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19007 | hp2 | a0001 | c0002 | t0007 | g0246 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19010 | hp2 | a0001 | c0002 | t0007 | g0243 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19012 | hp2 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19030 | hp1 | a0002 | c0001 | t0014 | g0055 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0113 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19054 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19054 | hp2 | a0001 | c0002 | t0005 | g0161 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19055 | hp2 | a0001 | c0002 | t0005 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0186 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19057 | hp2 | a0001 | c0002 | t0007 | g0245 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0083 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19065 | hp2 | a0001 | c0003 | t0002 | g0084 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0094 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19070 | hp1 | a0001 | c0002 | t0005 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0198 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0091 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19078 | hp2 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19079 | hp1 | a0001 | c0002 | t0005 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19085 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19087 | hp1 | a0001 | c0002 | t0005 | g0160 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19088 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0041 | AFR | ASW | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0077 | AFR | ASW | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0239 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0162 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0032 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0063 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0066 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0174 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | USA | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0201 | AFR | USA | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0110 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0006 | g0137 | REF | REF | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0076 | REF | REF | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45732099 | G | A | 1 | a0003 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.1048G>A | p.Asp350Asn | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/20 | 1118/3574 | 1048/1764 | 350/587 | chr3 | 45732099 | |||
| chr3:45737644 | A | T | 2 | a0001 a0003 |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
missense_variant | MODERATE | c.1301A>T | p.Tyr434Phe | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 15/20 | 1371/3574 | 1301/1764 | 434/587 | chr3 | 45737644 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45713193 | A | G | 2 | a0001c0003 a0001c0006 |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
synonymous_variant | LOW | c.540A>G | p.Pro180Pro | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/20 | 610/3574 | 540/1764 | 180/587 | chr3 | 45713193 | |||
| chr3:45731339 | A | G | 1 | a0001c0004 | 2 | HG02970.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.960A>G | p.Thr320Thr | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/20 | 1030/3574 | 960/1764 | 320/587 | chr3 | 45731339 | |||
| chr3:45732074 | T | C | 1 | a0001c0006 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.1023T>C | p.His341His | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/20 | 1093/3574 | 1023/1764 | 341/587 | chr3 | 45732074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45689427 | G | A | 1 | a0002c0001t0008 | 3 | HG01257.hp2 HG01258.hp1 HG01358.hp1 |
5_prime_UTR_variant | MODIFIER | c.-39G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/20 | 39 | chr3 | 45689427 | ||||||
| chr3:45689445 | G | A | 1 | a0001c0002t0012 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/20 | 21 | chr3 | 45689445 | ||||||
| chr3:45743965 | A | G | 1 | a0001c0002t0011 | 2 | HG02886.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 296 | chr3 | 45743965 | ||||||
| chr3:45744274 | G | A | 1 | a0001c0002t0013 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 605 | chr3 | 45744274 | ||||||
| chr3:45744423 | T | G | 2 | a0001c0002t0006 a0001c0002t0013 |
4 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*754T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 754 | chr3 | 45744423 | ||||||
| chr3:45744474 | C | G | 2 | a0001c0002t0003 a0001c0002t0005 |
40 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*805C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 805 | chr3 | 45744474 | ||||||
| chr3:45744556 | C | G | 1 | a0001c0002t0007 | 4 | HG00597.hp2 NA19007.hp2 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 887 | chr3 | 45744556 | ||||||
| chr3:45744615 | A | G | 1 | a0001c0003t0015 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 946 | chr3 | 45744615 | ||||||
| chr3:45744828 | A | T | 1 | a0002c0001t0010 | 2 | HG00609.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1159A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1159 | chr3 | 45744828 | ||||||
| chr3:45744847 | T | TA | 14 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(11): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1181dupA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1182 | INFO_REALIGN_3_PRIME | chr3 | 45744847 | |||||
| chr3:45744851 | T | C | 14 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(11): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1182T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1182 | chr3 | 45744851 | ||||||
| chr3:45744856 | C | T | 1 | a0002c0001t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1187 | chr3 | 45744856 | ||||||
| chr3:45744913 | T | C | 1 | a0002c0001t0009 | 2 | HG01243.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1244 | chr3 | 45744913 | ||||||
| chr3:45745006 | TTAATA | T | 1 | a0001c0002t0003 | 23 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1341_*1345delTATA others(1): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1341 | INFO_REALIGN_3_PRIME | chr3 | 45745006 | |||||
| chr3:45745012 | T | G | 1 | a0002c0001t0010 | 2 | HG00609.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1343T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1343 | chr3 | 45745012 | ||||||
| chr3:45745108 | A | T | 1 | a0001c0002t0004 | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1439A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1439 | chr3 | 45745108 | ||||||
| chr3:45745389 | A | G | 1 | a0001c0002t0004 | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1720A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1720 | chr3 | 45745389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45689584 | G | C | 1 | a0002c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.32+87G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689584 | |||||||
| chr3:45689771 | G | T | 11 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(8): Show |
12 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+274G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689771 | |||||||
| chr3:45689783 | A | G | 76 | a0001c0002t0011g0049 a0002c0001t0001g0001 a0002c0001t0001g0005 others(73): Show |
111 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.32+286A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689783 | |||||||
| chr3:45689862 | A | G | 23 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(20): Show |
30 | HG00438.hp1 HG00597.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+365A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689862 | |||||||
| chr3:45689912 | A | G | 1 | a0002c0001t0001g0241 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.32+415A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689912 | |||||||
| chr3:45689959 | C | T | 99 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(96): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.32+462C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689959 | |||||||
| chr3:45689972 | G | GC | 5 | a0001c0003t0002g0022 a0001c0003t0002g0051 a0001c0003t0002g0052 others(2): Show |
6 | HG01074.hp2 HG01243.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+480dupC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45689972 | ||||||
| chr3:45689976 | C | G | 1 | a0002c0001t0001g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+479C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689976 | |||||||
| chr3:45690089 | A | G | 1 | a0001c0004t0002g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.32+592A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690089 | |||||||
| chr3:45690152 | C | G | 1 | a0002c0001t0001g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.32+655C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690152 | |||||||
| chr3:45690240 | A | C | 43 | a0001c0002t0002g0004 a0001c0002t0002g0034 a0001c0002t0002g0035 others(40): Show |
63 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.32+743A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690240 | |||||||
| chr3:45690292 | T | C | 98 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(95): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.32+795T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690292 | |||||||
| chr3:45690297 | T | C | 1 | a0002c0001t0001g0179 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.32+800T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690297 | |||||||
| chr3:45690428 | C | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+931C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690428 | |||||||
| chr3:45690437 | G | A | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+940G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690437 | |||||||
| chr3:45690552 | T | C | 35 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(32): Show |
48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.32+1055T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690552 | |||||||
| chr3:45690571 | A | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+1074A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690571 | |||||||
| chr3:45690710 | C | T | 9 | a0001c0003t0002g0022 a0001c0003t0002g0031 a0001c0003t0002g0051 others(6): Show |
11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+1213C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690710 | |||||||
| chr3:45690716 | CCTCCACA others(7): Show |
C | 121 | a0001c0002t0004g0102 a0001c0003t0002g0003 a0001c0003t0002g0007 others(118): Show |
171 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.32+1226_32+1239del others(14): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45690716 | ||||||
| chr3:45690745 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+1248A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690745 | |||||||
| chr3:45690917 | G | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+1420G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690917 | |||||||
| chr3:45690926 | G | GT | 23 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0015 others(20): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.32+1430dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45690926 | ||||||
| chr3:45690941 | G | A | 1 | a0002c0001t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.32+1444G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690941 | |||||||
| chr3:45690974 | A | C | 1 | a0001c0003t0002g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.32+1477A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690974 | |||||||
| chr3:45691023 | T | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+1526T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691023 | |||||||
| chr3:45691074 | T | C | 1 | a0001c0002t0002g0242 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.32+1577T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691074 | |||||||
| chr3:45691105 | C | G | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+1608C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691105 | |||||||
| chr3:45691256 | A | T | 1 | a0001c0002t0005g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.32+1759A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691256 | |||||||
| chr3:45691328 | G | A | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+1831G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691328 | |||||||
| chr3:45691598 | G | GT | 14 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(11): Show |
16 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+2111dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45691598 | ||||||
| chr3:45691598 | G | GTT | 90 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(87): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.32+2110_32+2111dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45691598 | ||||||
| chr3:45691599 | T | C | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+2102T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691599 | |||||||
| chr3:45691759 | T | A | 1 | a0002c0001t0001g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.32+2262T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691759 | |||||||
| chr3:45691938 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+2441A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691938 | |||||||
| chr3:45691963 | A | G | 1 | a0002c0001t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.32+2466A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691963 | |||||||
| chr3:45692026 | C | T | 2 | a0001c0003t0002g0100 a0001c0003t0002g0101 |
2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.32+2529C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692026 | |||||||
| chr3:45692114 | G | A | 1 | a0002c0001t0001g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.32+2617G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692114 | |||||||
| chr3:45692149 | C | G | 3 | a0002c0001t0001g0237 a0002c0001t0001g0238 a0002c0001t0001g0239 |
3 | HG01261.hp2 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.32+2652C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692149 | |||||||
| chr3:45692219 | G | A | 91 | a0001c0002t0004g0102 a0001c0003t0002g0022 a0001c0003t0002g0031 others(88): Show |
128 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.32+2722G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692219 | |||||||
| chr3:45692316 | GT | G | 29 | a0002c0001t0001g0006 a0002c0001t0001g0023 a0002c0001t0001g0024 others(26): Show |
37 | HG00609.hp2 HG00738.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.32+2834delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45692316 | ||||||
| chr3:45692335 | A | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+2838A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692335 | |||||||
| chr3:45692766 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+3269A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692766 | |||||||
| chr3:45692912 | G | A | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+3415G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692912 | |||||||
| chr3:45692992 | A | C | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.32+3495A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692992 | |||||||
| chr3:45693266 | G | A | 7 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(4): Show |
11 | HG02257.hp1 HG02559.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+3769G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693266 | |||||||
| chr3:45693326 | T | C | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+3829T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693326 | |||||||
| chr3:45693416 | G | T | 1 | a0001c0002t0004g0042 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.32+3919G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693416 | |||||||
| chr3:45693483 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+3986A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693483 | |||||||
| chr3:45693650 | T | C | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+4153T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693650 | |||||||
| chr3:45693660 | A | G | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+4163A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693660 | |||||||
| chr3:45693664 | A | G | 1 | a0001c0002t0004g0174 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.32+4167A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693664 | |||||||
| chr3:45693700 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+4203A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693700 | |||||||
| chr3:45693726 | G | A | 35 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(32): Show |
48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.32+4229G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693726 | |||||||
| chr3:45693793 | A | G | 1 | a0001c0003t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.32+4296A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693793 | |||||||
| chr3:45694025 | G | A | 1 | a0002c0001t0001g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.32+4528G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694025 | |||||||
| chr3:45694087 | G | A | 26 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(23): Show |
37 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.32+4590G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694087 | |||||||
| chr3:45694118 | T | C | 2 | a0001c0002t0002g0034 a0001c0002t0002g0035 |
4 | NA18939.hp2 NA18985.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+4621T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694118 | |||||||
| chr3:45694126 | A | C | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+4629A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694126 | |||||||
| chr3:45694238 | T | A | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+4741T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694238 | |||||||
| chr3:45694409 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+4912A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694409 | |||||||
| chr3:45694652 | T | A | 1 | a0001c0003t0002g0078 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+5155T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694652 | |||||||
| chr3:45694686 | G | A | 3 | a0001c0002t0004g0102 a0002c0001t0009g0103 a0002c0001t0009g0104 |
3 | HG01243.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.32+5189G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694686 | |||||||
| chr3:45694768 | A | G | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.32+5271A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694768 | |||||||
| chr3:45694931 | A | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+5434A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694931 | |||||||
| chr3:45694971 | A | C | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+5474A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694971 | |||||||
| chr3:45695026 | G | C | 1 | a0001c0003t0002g0079 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.32+5529G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695026 | |||||||
| chr3:45695130 | A | G | 1 | a0002c0001t0001g0236 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.32+5633A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695130 | |||||||
| chr3:45695266 | CT | C | 76 | a0002c0001t0001g0001 a0002c0001t0001g0005 a0002c0001t0001g0012 others(73): Show |
111 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.32+5781delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45695266 | ||||||
| chr3:45695330 | G | A | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.32+5833G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695330 | |||||||
| chr3:45695421 | C | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+5924C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695421 | |||||||
| chr3:45695469 | C | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+5972C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695469 | |||||||
| chr3:45695484 | C | T | 12 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(9): Show |
18 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+5987C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695484 | |||||||
| chr3:45695615 | A | C | 1 | a0002c0001t0001g0234 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.32+6118A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695615 | |||||||
| chr3:45695629 | C | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+6132C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695629 | |||||||
| chr3:45695768 | C | T | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+6271C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695768 | |||||||
| chr3:45695803 | T | A | 2 | a0002c0001t0001g0023 a0002c0001t0001g0056 |
3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.32+6306T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695803 | |||||||
| chr3:45695858 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+6361G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695858 | |||||||
| chr3:45695950 | A | G | 2 | a0001c0004t0002g0136 a0001c0004t0002g0171 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.32+6453A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695950 | |||||||
| chr3:45695975 | G | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+6478G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695975 | |||||||
| chr3:45695997 | CTT | C | 41 | a0001c0002t0002g0004 a0001c0002t0002g0034 a0001c0002t0002g0035 others(38): Show |
61 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.32+6517_32+6518del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45695997 | ||||||
| chr3:45695997 | CTTTT | C | 7 | a0001c0002t0004g0102 a0002c0001t0001g0030 a0002c0001t0001g0105 others(4): Show |
8 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+6515_32+6518del others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45695997 | ||||||
| chr3:45696137 | T | G | 1 | a0001c0002t0003g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.32+6640T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696137 | |||||||
| chr3:45696221 | T | C | 3 | a0001c0003t0002g0028 a0001c0003t0002g0080 a0001c0003t0002g0081 |
4 | HG01109.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+6724T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696221 | |||||||
| chr3:45696233 | G | A | 1 | a0001c0002t0012g0120 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.32+6736G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696233 | |||||||
| chr3:45696310 | C | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.32+6813C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696310 | |||||||
| chr3:45696326 | T | A | 1 | a0001c0002t0004g0018 | 3 | HG02109.hp2 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.32+6829T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696326 | |||||||
| chr3:45696352 | C | T | 43 | a0001c0002t0002g0004 a0001c0002t0002g0034 a0001c0002t0002g0035 others(40): Show |
63 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.32+6855C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696352 | |||||||
| chr3:45696399 | G | A | 2 | a0002c0001t0001g0105 a0002c0001t0001g0106 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.32+6902G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696399 | |||||||
| chr3:45696522 | A | G | 1 | a0001c0003t0015g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.33-6916A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696522 | |||||||
| chr3:45696615 | C | T | 35 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(32): Show |
48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-6823C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696615 | |||||||
| chr3:45696741 | A | G | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-6697A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696741 | |||||||
| chr3:45696764 | C | T | 12 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(9): Show |
18 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-6674C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696764 | |||||||
| chr3:45697141 | T | G | 8 | a0002c0001t0001g0024 a0002c0001t0001g0057 a0002c0001t0001g0058 others(5): Show |
9 | HG02055.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-6297T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697141 | |||||||
| chr3:45697199 | G | A | 4 | a0001c0002t0002g0140 a0001c0002t0002g0141 a0001c0002t0002g0142 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6239G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697199 | |||||||
| chr3:45697267 | TC | T | 4 | a0001c0002t0002g0144 a0001c0002t0003g0145 a0001c0002t0003g0168 others(1): Show |
4 | HG01069.hp1 HG02165.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6169delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697267 | ||||||
| chr3:45697268 | C | CT | 11 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0036 others(8): Show |
12 | HG00558.hp1 HG01361.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-6170_33-6169ins others(1): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697268 | |||||||
| chr3:45697269 | C | CT | 14 | a0001c0002t0002g0119 a0001c0002t0002g0133 a0001c0002t0002g0134 others(11): Show |
17 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-6144dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | C | CTT | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.33-6145_33-6144dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | C | CTTTT | 14 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(11): Show |
15 | HG00438.hp1 HG00597.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.33-6147_33-6144dup others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | C | CTTTTT | 26 | a0001c0002t0002g0248 a0001c0002t0002g0249 a0001c0003t0002g0003 others(23): Show |
38 | HG00438.hp2 HG00621.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.33-6148_33-6144dup others(5): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | C | CTTTTTTT others(4): Show |
1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-6154_33-6144dup others(11): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | C | CTTTTTTT others(5): Show |
1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-6155_33-6144dup others(12): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | C | T | 39 | a0001c0002t0002g0004 a0001c0002t0002g0034 a0001c0002t0002g0035 others(36): Show |
59 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.33-6169C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697269 | |||||||
| chr3:45697269 | CT | C | 7 | a0001c0002t0002g0121 a0002c0001t0001g0043 a0002c0001t0001g0183 others(4): Show |
8 | HG00738.hp1 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-6144delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | CTTTTTTT others(2): Show |
C | 12 | a0001c0002t0004g0102 a0001c0003t0002g0022 a0001c0003t0002g0031 others(9): Show |
14 | HG01074.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-6152_33-6144del others(9): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697269 | CTTTTTTT others(3): Show |
C | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-6153_33-6144del others(10): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | ||||||
| chr3:45697655 | G | T | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-5783G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697655 | |||||||
| chr3:45698119 | A | G | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-5319A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698119 | |||||||
| chr3:45698272 | C | G | 3 | a0002c0001t0001g0229 a0002c0001t0001g0230 a0002c0001t0001g0236 |
3 | NA18977.hp1 NA19012.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.33-5166C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698272 | |||||||
| chr3:45698315 | G | T | 84 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(81): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-5123G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698315 | |||||||
| chr3:45698355 | C | G | 2 | a0002c0001t0001g0023 a0002c0001t0001g0056 |
3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.33-5083C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698355 | |||||||
| chr3:45698623 | T | TCACTGCA others(9): Show |
1 | a0002c0001t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.33-4814_33-4799dup others(16): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45698623 | ||||||
| chr3:45698707 | T | C | 76 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(73): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.33-4731T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698707 | |||||||
| chr3:45698786 | T | C | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-4652T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698786 | |||||||
| chr3:45698807 | A | G | 86 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(83): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.33-4631A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698807 | |||||||
| chr3:45698896 | G | A | 3 | a0001c0002t0002g0015 a0001c0002t0002g0122 a0001c0002t0002g0123 |
5 | HG00639.hp2 HG01192.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-4542G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698896 | |||||||
| chr3:45698918 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-4520G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698918 | |||||||
| chr3:45699009 | G | A | 1 | a0002c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.33-4429G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699009 | |||||||
| chr3:45699066 | T | C | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-4372T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699066 | |||||||
| chr3:45699257 | A | G | 2 | a0001c0003t0002g0008 a0001c0003t0002g0079 |
5 | NA18954.hp1 NA18964.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-4181A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699257 | |||||||
| chr3:45699284 | A | T | 26 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(23): Show |
37 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-4154A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699284 | |||||||
| chr3:45699288 | T | A | 148 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(145): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.33-4150T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699288 | |||||||
| chr3:45699304 | A | T | 1 | a0001c0002t0003g0166 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.33-4134A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699304 | |||||||
| chr3:45699341 | A | T | 1 | a0002c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.33-4097A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699341 | |||||||
| chr3:45699371 | G | A | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.33-4067G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699371 | |||||||
| chr3:45699468 | A | AAAATTAT | 236 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(233): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.33-3963_33-3957dup others(7): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45699468 | ||||||
| chr3:45699490 | T | C | 1 | a0001c0002t0005g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.33-3948T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699490 | |||||||
| chr3:45699551 | T | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-3887T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699551 | |||||||
| chr3:45699608 | A | G | 149 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(146): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.33-3830A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699608 | |||||||
| chr3:45699695 | T | G | 3 | a0002c0001t0001g0237 a0002c0001t0001g0238 a0002c0001t0001g0239 |
3 | HG01261.hp2 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.33-3743T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699695 | |||||||
| chr3:45699727 | G | A | 2 | a0002c0001t0001g0064 a0002c0001t0001g0235 |
2 | NA18966.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.33-3711G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699727 | |||||||
| chr3:45699727 | G | T | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-3711G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699727 | |||||||
| chr3:45699765 | G | T | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.33-3673G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699765 | |||||||
| chr3:45699768 | C | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-3670C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699768 | |||||||
| chr3:45699905 | T | C | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.33-3533T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699905 | |||||||
| chr3:45700150 | C | T | 1 | a0002c0001t0009g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.33-3288C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700150 | |||||||
| chr3:45700241 | A | G | 1 | a0002c0001t0001g0225 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.33-3197A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700241 | |||||||
| chr3:45700529 | G | A | 1 | a0001c0002t0002g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.33-2909G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700529 | |||||||
| chr3:45700753 | A | G | 1 | a0002c0001t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.33-2685A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700753 | |||||||
| chr3:45700826 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.33-2612C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700826 | |||||||
| chr3:45700869 | A | G | 1 | a0001c0003t0002g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.33-2569A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700869 | |||||||
| chr3:45700932 | A | C | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-2506A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700932 | |||||||
| chr3:45701312 | C | G | 28 | a0001c0002t0003g0002 a0001c0002t0003g0038 a0001c0002t0003g0139 others(25): Show |
40 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.33-2126C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701312 | |||||||
| chr3:45701361 | T | C | 3 | a0001c0002t0002g0114 a0001c0002t0002g0115 a0001c0002t0002g0118 |
3 | HG01168.hp1 HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.33-2077T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701361 | |||||||
| chr3:45701502 | G | A | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-1936G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701502 | |||||||
| chr3:45701559 | T | C | 1 | a0002c0001t0001g0189 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.33-1879T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701559 | |||||||
| chr3:45701621 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-1817A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701621 | |||||||
| chr3:45701785 | G | A | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.33-1653G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701785 | |||||||
| chr3:45701857 | C | T | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-1581C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701857 | |||||||
| chr3:45701898 | G | T | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-1540G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701898 | |||||||
| chr3:45702052 | A | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-1386A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702052 | |||||||
| chr3:45702146 | A | C | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-1292A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702146 | |||||||
| chr3:45702163 | G | C | 1 | a0001c0002t0002g0124 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.33-1275G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702163 | |||||||
| chr3:45702182 | GT | G | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-1255delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702182 | |||||||
| chr3:45702215 | G | A | 236 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(233): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.33-1223G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702215 | |||||||
| chr3:45702421 | A | G | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-1017A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702421 | |||||||
| chr3:45702424 | C | A | 2 | a0001c0004t0002g0136 a0001c0004t0002g0171 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.33-1014C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702424 | |||||||
| chr3:45702596 | A | G | 1 | a0002c0001t0001g0223 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.33-842A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702596 | |||||||
| chr3:45702698 | C | G | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.33-740C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702698 | |||||||
| chr3:45702727 | T | C | 4 | a0001c0002t0002g0140 a0001c0002t0002g0141 a0001c0002t0002g0142 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-711T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702727 | |||||||
| chr3:45702756 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-682G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702756 | |||||||
| chr3:45702785 | A | G | 2 | a0001c0004t0002g0136 a0001c0004t0002g0171 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.33-653A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702785 | |||||||
| chr3:45702800 | C | T | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-638C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702800 | |||||||
| chr3:45703014 | C | T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0121 |
3 | HG00738.hp1 HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.33-424C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703014 | |||||||
| chr3:45703019 | G | A | 1 | a0002c0001t0001g0189 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.33-419G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703019 | |||||||
| chr3:45703047 | G | T | 1 | a0001c0003t0002g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.33-391G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703047 | |||||||
| chr3:45703106 | C | T | 1 | a0001c0002t0003g0165 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.33-332C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703106 | |||||||
| chr3:45703154 | T | G | 1 | a0001c0002t0002g0009 | 4 | HG01106.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-284T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703154 | |||||||
| chr3:45703201 | AT | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.33-230delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45703201 | ||||||
| chr3:45703582 | A | C | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+47A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45703582 | |||||||
| chr3:45703590 | C | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+55C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45703590 | |||||||
| chr3:45704227 | C | T | 1 | a0002c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130+692C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704227 | |||||||
| chr3:45704281 | G | A | 2 | a0002c0001t0001g0183 a0002c0001t0001g0190 |
2 | NA18941.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.130+746G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704281 | |||||||
| chr3:45704281 | G | C | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.130+746G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704281 | |||||||
| chr3:45704352 | G | A | 1 | a0002c0001t0001g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.131-783G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704352 | |||||||
| chr3:45704353 | G | A | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.131-782G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704353 | |||||||
| chr3:45704368 | G | A | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.131-767G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704368 | |||||||
| chr3:45704400 | G | A | 1 | a0002c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.131-735G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704400 | |||||||
| chr3:45704412 | G | A | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.131-723G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704412 | |||||||
| chr3:45704518 | A | G | 9 | a0001c0003t0002g0022 a0001c0003t0002g0031 a0001c0003t0002g0051 others(6): Show |
11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.131-617A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704518 | |||||||
| chr3:45704872 | T | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.131-263T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704872 | |||||||
| chr3:45704873 | T | C | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.131-262T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704873 | |||||||
| chr3:45705108 | T | C | 1 | a0001c0003t0015g0053 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.131-27T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45705108 | |||||||
| chr3:45705344 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.205+135A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705344 | |||||||
| chr3:45705496 | A | AT | 48 | a0001c0002t0002g0118 a0001c0002t0002g0119 a0001c0002t0005g0164 others(45): Show |
67 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.205+310dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 45705496 | ||||||
| chr3:45705496 | AT | A | 32 | a0001c0002t0002g0034 a0001c0002t0002g0125 a0001c0002t0002g0144 others(29): Show |
44 | HG00099.hp2 HG00558.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.205+310delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 45705496 | ||||||
| chr3:45705588 | C | T | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.205+379C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705588 | |||||||
| chr3:45705645 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+436G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705645 | |||||||
| chr3:45705860 | G | A | 2 | a0002c0001t0001g0105 a0002c0001t0001g0106 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.205+651G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705860 | |||||||
| chr3:45705933 | G | A | 1 | a0002c0001t0001g0065 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.205+724G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705933 | |||||||
| chr3:45706005 | C | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.206-775C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706005 | |||||||
| chr3:45706172 | G | T | 1 | a0001c0003t0002g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.206-608G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706172 | |||||||
| chr3:45706408 | G | T | 1 | a0002c0001t0001g0044 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.206-372G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706408 | |||||||
| chr3:45706460 | C | T | 1 | a0002c0001t0001g0239 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.206-320C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706460 | |||||||
| chr3:45706517 | C | G | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-263C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706517 | |||||||
| chr3:45706937 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.333+30G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45706937 | |||||||
| chr3:45706943 | A | G | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.333+36A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45706943 | |||||||
| chr3:45707107 | T | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.333+200T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707107 | |||||||
| chr3:45707140 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.333+233A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707140 | |||||||
| chr3:45707488 | T | C | 1 | a0001c0002t0002g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.333+581T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707488 | |||||||
| chr3:45707602 | A | T | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.333+695A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707602 | |||||||
| chr3:45707691 | G | A | 9 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0036 others(6): Show |
13 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.333+784G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707691 | |||||||
| chr3:45707810 | A | G | 1 | a0001c0002t0002g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.333+903A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707810 | |||||||
| chr3:45707973 | A | G | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.333+1066A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707973 | |||||||
| chr3:45708055 | AC | A | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.333+1149delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708055 | |||||||
| chr3:45708185 | G | C | 1 | a0001c0003t0002g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.333+1278G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708185 | |||||||
| chr3:45708230 | T | C | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.334-1268T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708230 | |||||||
| chr3:45708344 | T | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.334-1154T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708344 | |||||||
| chr3:45708406 | A | G | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1092A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708406 | |||||||
| chr3:45708488 | G | T | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-1010G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708488 | |||||||
| chr3:45708523 | C | T | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.334-975C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708523 | |||||||
| chr3:45708708 | C | T | 9 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0036 others(6): Show |
13 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.334-790C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708708 | |||||||
| chr3:45708767 | T | C | 19 | a0001c0002t0003g0002 a0001c0002t0003g0038 a0001c0002t0003g0139 others(16): Show |
28 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.334-731T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708767 | |||||||
| chr3:45708791 | T | G | 1 | a0002c0001t0001g0227 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.334-707T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708791 | |||||||
| chr3:45709382 | C | T | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.334-116C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45709382 | |||||||
| chr3:45709494 | A | G | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
splice_region_variant&intron_variant | LOW | c.334-4A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45709494 | |||||||
| chr3:45709737 | C | T | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.483+90C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45709737 | |||||||
| chr3:45709944 | A | G | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.483+297A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45709944 | |||||||
| chr3:45710224 | A | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.483+577A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710224 | |||||||
| chr3:45710271 | G | A | 2 | a0001c0002t0002g0127 a0001c0002t0002g0133 |
2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.483+624G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710271 | |||||||
| chr3:45710498 | G | A | 3 | a0001c0002t0002g0110 a0001c0002t0002g0111 a0001c0002t0002g0112 |
3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483+851G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710498 | |||||||
| chr3:45710500 | C | CT | 87 | a0001c0003t0002g0022 a0001c0003t0002g0031 a0001c0003t0002g0051 others(84): Show |
124 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.483+871dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | ||||||
| chr3:45710500 | C | CTT | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
42 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.483+870_483+871dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | ||||||
| chr3:45710500 | C | CTTT | 5 | a0001c0003t0002g0013 a0001c0003t0002g0095 a0001c0003t0002g0096 others(2): Show |
7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+869_483+871dup others(3): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | ||||||
| chr3:45710500 | CT | C | 90 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(87): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.483+871delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | ||||||
| chr3:45710535 | A | G | 1 | a0002c0001t0001g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.483+888A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710535 | |||||||
| chr3:45710597 | G | A | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.483+950G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710597 | |||||||
| chr3:45710737 | G | T | 101 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(98): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.483+1090G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710737 | |||||||
| chr3:45710801 | C | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.483+1154C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710801 | |||||||
| chr3:45710848 | G | T | 1 | a0002c0001t0001g0030 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.483+1201G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710848 | |||||||
| chr3:45710951 | G | A | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.483+1304G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710951 | |||||||
| chr3:45710979 | C | T | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.483+1332C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710979 | |||||||
| chr3:45711119 | T | C | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.483+1472T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711119 | |||||||
| chr3:45711158 | T | C | 1 | a0002c0001t0001g0197 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.483+1511T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711158 | |||||||
| chr3:45711392 | C | T | 2 | a0001c0002t0003g0157 a0001c0002t0003g0158 |
2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.483+1745C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711392 | |||||||
| chr3:45711421 | G | A | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-1716G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711421 | |||||||
| chr3:45711542 | C | T | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.484-1595C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711542 | |||||||
| chr3:45711694 | A | G | 3 | a0001c0002t0005g0146 a0001c0002t0005g0162 a0001c0002t0005g0163 |
3 | HG02735.hp2 HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.484-1443A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711694 | |||||||
| chr3:45711719 | A | G | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.484-1418A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711719 | |||||||
| chr3:45711803 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.484-1334G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711803 | |||||||
| chr3:45711995 | C | T | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.484-1142C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711995 | |||||||
| chr3:45712047 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.484-1090A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712047 | |||||||
| chr3:45712087 | A | G | 236 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(233): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.484-1050A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712087 | |||||||
| chr3:45712172 | GC | G | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.484-964delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712172 | |||||||
| chr3:45712173 | C | G | 89 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(86): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.484-964C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712173 | |||||||
| chr3:45712501 | G | A | 1 | a0001c0002t0005g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.484-636G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712501 | |||||||
| chr3:45712528 | G | A | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.484-609G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712528 | |||||||
| chr3:45712715 | A | G | 3 | a0001c0002t0002g0110 a0001c0002t0002g0111 a0001c0002t0002g0112 |
3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.484-422A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712715 | |||||||
| chr3:45712740 | C | T | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.484-397C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712740 | |||||||
| chr3:45712810 | T | TTAG | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.484-325_484-323dup others(3): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45712810 | ||||||
| chr3:45712995 | C | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.484-142C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712995 | |||||||
| chr3:45713067 | G | A | 1 | a0002c0001t0001g0179 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.484-70G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45713067 | |||||||
| chr3:45713257 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.543+61G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713257 | |||||||
| chr3:45713267 | G | A | 1 | a0002c0001t0001g0198 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.543+71G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713267 | |||||||
| chr3:45713511 | G | A | 3 | a0002c0001t0001g0199 a0002c0001t0001g0200 a0002c0001t0001g0240 |
3 | NA18991.hp1 NA18998.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.543+315G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713511 | |||||||
| chr3:45713646 | A | G | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.544-400A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713646 | |||||||
| chr3:45714144 | G | C | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.577+65G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714144 | |||||||
| chr3:45714238 | T | G | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(100): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.577+159T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714238 | |||||||
| chr3:45714239 | TTG | T | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(101): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.577+162_577+163del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45714239 | ||||||
| chr3:45714240 | TG | T | 123 | a0001c0002t0007g0021 a0001c0003t0002g0003 a0001c0003t0002g0007 others(120): Show |
174 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.577+162delG | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714240 | |||||||
| chr3:45714241 | G | T | 9 | a0002c0001t0001g0030 a0002c0001t0001g0063 a0002c0001t0001g0105 others(6): Show |
10 | HG01243.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.577+162G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714241 | |||||||
| chr3:45714246 | T | G | 1 | a0001c0003t0002g0109 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.577+167T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714246 | |||||||
| chr3:45714436 | A | C | 1 | a0002c0001t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.577+357A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714436 | |||||||
| chr3:45714482 | G | A | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.577+403G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714482 | |||||||
| chr3:45714778 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.577+699G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714778 | |||||||
| chr3:45714804 | A | C | 1 | a0002c0001t0001g0226 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.577+725A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714804 | |||||||
| chr3:45714818 | A | C | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.577+739A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714818 | |||||||
| chr3:45714858 | C | G | 107 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(104): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.577+779C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714858 | |||||||
| chr3:45714902 | C | T | 1 | a0002c0001t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.577+823C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714902 | |||||||
| chr3:45714903 | G | A | 1 | a0001c0002t0002g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.577+824G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714903 | |||||||
| chr3:45714997 | A | G | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577+918A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714997 | |||||||
| chr3:45715059 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.577+980G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715059 | |||||||
| chr3:45715071 | T | C | 1 | a0002c0001t0001g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.577+992T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715071 | |||||||
| chr3:45715081 | C | T | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577+1002C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715081 | |||||||
| chr3:45715088 | C | T | 1 | a0001c0003t0002g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.577+1009C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715088 | |||||||
| chr3:45715097 | G | A | 1 | a0001c0002t0002g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.577+1018G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715097 | |||||||
| chr3:45715158 | C | T | 6 | a0002c0001t0001g0012 a0002c0001t0001g0182 a0002c0001t0001g0198 others(3): Show |
9 | HG00423.hp2 HG01975.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.577+1079C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715158 | |||||||
| chr3:45715191 | G | C | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.577+1112G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715191 | |||||||
| chr3:45715230 | G | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.577+1151G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715230 | |||||||
| chr3:45715233 | G | C | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.577+1154G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715233 | |||||||
| chr3:45715314 | C | A | 1 | a0002c0001t0001g0199 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.577+1235C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715314 | |||||||
| chr3:45715364 | A | G | 2 | a0002c0001t0001g0187 a0002c0001t0001g0215 |
2 | NA18747.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.577+1285A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715364 | |||||||
| chr3:45715435 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.577+1356C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715435 | |||||||
| chr3:45715494 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.577+1415A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715494 | |||||||
| chr3:45715497 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.577+1418C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715497 | |||||||
| chr3:45715500 | G | T | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.577+1421G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715500 | |||||||
| chr3:45715547 | C | T | 1 | a0002c0001t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.577+1468C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715547 | |||||||
| chr3:45715613 | A | G | 1 | a0001c0002t0002g0150 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.577+1534A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715613 | |||||||
| chr3:45715635 | G | A | 1 | a0002c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.577+1556G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715635 | |||||||
| chr3:45715706 | G | A | 5 | a0001c0002t0002g0014 a0001c0002t0002g0116 a0001c0002t0002g0117 others(2): Show |
6 | HG00735.hp2 HG01123.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.577+1627G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715706 | |||||||
| chr3:45715773 | CA | C | 132 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(129): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.577+1709delA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45715773 | ||||||
| chr3:45715790 | T | C | 77 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(74): Show |
106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.577+1711T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715790 | |||||||
| chr3:45715925 | T | A | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.577+1846T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715925 | |||||||
| chr3:45716099 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.577+2020C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716099 | |||||||
| chr3:45716408 | T | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.577+2329T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716408 | |||||||
| chr3:45716504 | G | T | 1 | a0002c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.577+2425G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716504 | |||||||
| chr3:45716528 | T | G | 3 | a0001c0002t0002g0015 a0001c0002t0002g0122 a0001c0002t0002g0123 |
5 | HG00639.hp2 HG01192.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.577+2449T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716528 | |||||||
| chr3:45716584 | C | T | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577+2505C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716584 | |||||||
| chr3:45716889 | C | A | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.578-2611C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716889 | |||||||
| chr3:45717029 | G | A | 3 | a0002c0001t0001g0027 a0002c0001t0001g0075 a0002c0001t0001g0077 |
4 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-2471G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717029 | |||||||
| chr3:45717037 | T | C | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.578-2463T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717037 | |||||||
| chr3:45717103 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.578-2397T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717103 | |||||||
| chr3:45717359 | G | A | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-2141G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717359 | |||||||
| chr3:45717375 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.578-2125A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717375 | |||||||
| chr3:45717454 | G | C | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.578-2046G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717454 | |||||||
| chr3:45717461 | G | T | 1 | a0001c0002t0002g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.578-2039G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717461 | |||||||
| chr3:45717519 | C | T | 1 | a0001c0002t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.578-1981C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717519 | |||||||
| chr3:45717544 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.578-1956T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717544 | |||||||
| chr3:45717615 | A | G | 5 | a0002c0001t0001g0023 a0002c0001t0001g0056 a0002c0001t0001g0058 others(2): Show |
6 | HG01884.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.578-1885A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717615 | |||||||
| chr3:45717724 | T | C | 1 | a0002c0001t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.578-1776T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717724 | |||||||
| chr3:45717791 | C | T | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.578-1709C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717791 | |||||||
| chr3:45717871 | G | T | 1 | a0001c0003t0002g0052 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.578-1629G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717871 | |||||||
| chr3:45717944 | A | T | 1 | a0002c0001t0001g0214 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.578-1556A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717944 | |||||||
| chr3:45718006 | A | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.578-1494A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718006 | |||||||
| chr3:45718046 | T | C | 1 | a0002c0001t0001g0196 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.578-1454T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718046 | |||||||
| chr3:45718084 | A | G | 1 | a0001c0002t0002g0143 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.578-1416A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718084 | |||||||
| chr3:45718162 | A | G | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.578-1338A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718162 | |||||||
| chr3:45718294 | TA | T | 56 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(53): Show |
72 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.578-1192delA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45718294 | ||||||
| chr3:45718294 | TAA | T | 94 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(91): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.578-1193_578-1192d others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45718294 | ||||||
| chr3:45718330 | A | G | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.578-1170A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718330 | |||||||
| chr3:45718383 | T | C | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.578-1117T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718383 | |||||||
| chr3:45718432 | T | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.578-1068T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718432 | |||||||
| chr3:45718495 | A | C | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.578-1005A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718495 | |||||||
| chr3:45718503 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.578-997C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718503 | |||||||
| chr3:45718805 | A | G | 1 | a0001c0002t0003g0165 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.578-695A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718805 | |||||||
| chr3:45718991 | A | G | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.578-509A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718991 | |||||||
| chr3:45719108 | C | T | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.578-392C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719108 | |||||||
| chr3:45719237 | A | G | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.578-263A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719237 | |||||||
| chr3:45719314 | G | A | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-186G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719314 | |||||||
| chr3:45719492 | T | C | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.578-8T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719492 | |||||||
| chr3:45719623 | G | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.679+22G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45719623 | |||||||
| chr3:45719919 | G | C | 9 | a0001c0003t0002g0022 a0001c0003t0002g0031 a0001c0003t0002g0051 others(6): Show |
11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.679+318G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45719919 | |||||||
| chr3:45719950 | G | A | 5 | a0001c0003t0002g0013 a0001c0003t0002g0095 a0001c0003t0002g0096 others(2): Show |
7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+349G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45719950 | |||||||
| chr3:45720019 | T | C | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.679+418T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45720019 | |||||||
| chr3:45720439 | AC | A | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.679+843delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 45720439 | ||||||
| chr3:45720517 | C | G | 1 | a0001c0002t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.679+916C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45720517 | |||||||
| chr3:45720596 | T | C | 1 | a0002c0001t0001g0027 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.679+995T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45720596 | |||||||
| chr3:45721229 | T | C | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.680-771T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721229 | |||||||
| chr3:45721233 | C | T | 37 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0036 others(34): Show |
53 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.680-767C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721233 | |||||||
| chr3:45721271 | C | G | 1 | a0001c0002t0003g0156 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.680-729C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721271 | |||||||
| chr3:45721383 | G | A | 1 | a0001c0004t0002g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.680-617G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721383 | |||||||
| chr3:45721391 | G | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.680-609G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721391 | |||||||
| chr3:45721553 | T | C | 4 | a0002c0001t0001g0024 a0002c0001t0001g0060 a0002c0001t0001g0061 others(1): Show |
5 | HG02055.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-447T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721553 | |||||||
| chr3:45721554 | A | G | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.680-446A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721554 | |||||||
| chr3:45721577 | G | A | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.680-423G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721577 | |||||||
| chr3:45721643 | C | T | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.680-357C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721643 | |||||||
| chr3:45722143 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.765+58A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722143 | |||||||
| chr3:45722230 | A | G | 1 | a0002c0001t0001g0221 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.765+145A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722230 | |||||||
| chr3:45722407 | A | G | 1 | a0002c0001t0009g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.765+322A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722407 | |||||||
| chr3:45722443 | C | T | 1 | a0002c0001t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.765+358C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722443 | |||||||
| chr3:45722485 | G | A | 76 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(73): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.766-384G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722485 | |||||||
| chr3:45722672 | A | G | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.766-197A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722672 | |||||||
| chr3:45722754 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.766-115A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722754 | |||||||
| chr3:45723005 | G | A | 1 | a0001c0002t0005g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.852+50G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723005 | |||||||
| chr3:45723041 | G | A | 2 | a0002c0001t0008g0185 a0002c0001t0008g0202 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.852+86G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723041 | |||||||
| chr3:45723052 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.852+97T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723052 | |||||||
| chr3:45723078 | C | T | 1 | a0001c0002t0004g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.852+123C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723078 | |||||||
| chr3:45723187 | A | C | 1 | a0001c0002t0002g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.852+232A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723187 | |||||||
| chr3:45723200 | A | G | 1 | a0001c0002t0002g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.852+245A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723200 | |||||||
| chr3:45723233 | A | G | 1 | a0001c0002t0002g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.853-242A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723233 | |||||||
| chr3:45723437 | A | G | 4 | a0002c0001t0001g0065 a0002c0001t0001g0072 a0002c0001t0001g0074 others(1): Show |
4 | NA18747.hp1 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-38A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723437 | |||||||
| chr3:45723640 | T | G | 3 | a0001c0002t0006g0017 a0001c0002t0006g0148 a0001c0002t0013g0017 |
4 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+97T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723640 | |||||||
| chr3:45723696 | T | A | 4 | a0001c0003t0002g0022 a0001c0003t0002g0051 a0001c0003t0002g0052 others(1): Show |
5 | HG01074.hp2 HG01243.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+153T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723696 | |||||||
| chr3:45723729 | C | T | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.921+186C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723729 | |||||||
| chr3:45723780 | A | G | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.921+237A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723780 | |||||||
| chr3:45723904 | T | A | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+361T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723904 | |||||||
| chr3:45723948 | A | G | 1 | a0002c0001t0001g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.921+405A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723948 | |||||||
| chr3:45723959 | C | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.921+416C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723959 | |||||||
| chr3:45723965 | G | GAC | 90 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(87): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.921+440_921+441dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45723965 | ||||||
| chr3:45723965 | G | GACAC | 51 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(48): Show |
67 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.921+438_921+441dup others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45723965 | ||||||
| chr3:45724216 | C | T | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.921+673C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724216 | |||||||
| chr3:45724243 | A | G | 1 | a0001c0002t0005g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.921+700A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724243 | |||||||
| chr3:45724255 | A | G | 2 | a0002c0001t0001g0105 a0002c0001t0001g0106 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.921+712A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724255 | |||||||
| chr3:45724256 | G | A | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.921+713G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724256 | |||||||
| chr3:45724298 | G | GGT | 37 | a0001c0002t0002g0004 a0001c0002t0002g0112 a0001c0002t0002g0129 others(34): Show |
50 | HG00621.hp2 HG01074.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.921+790_921+791dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGT | 54 | a0001c0002t0002g0009 a0001c0002t0002g0014 a0001c0002t0002g0032 others(51): Show |
75 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.921+788_921+791dup others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGT | 84 | a0001c0002t0002g0035 a0001c0002t0002g0150 a0001c0002t0003g0002 others(81): Show |
131 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.921+786_921+791dup others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(1): Show |
23 | a0001c0002t0002g0144 a0001c0002t0002g0149 a0001c0002t0002g0248 others(20): Show |
29 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.921+784_921+791dup others(8): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(3): Show |
18 | a0001c0002t0002g0034 a0001c0002t0002g0242 a0001c0002t0003g0153 others(15): Show |
19 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.921+782_921+791dup others(10): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(5): Show |
3 | a0001c0002t0002g0036 a0001c0002t0002g0247 a0002c0001t0001g0214 |
4 | HG01361.hp2 HG01516.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+780_921+791dup others(12): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(7): Show |
5 | a0001c0002t0002g0021 a0001c0002t0002g0141 a0001c0002t0002g0142 others(2): Show |
6 | HG00438.hp1 HG00597.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+778_921+791dup others(14): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(9): Show |
4 | a0001c0002t0002g0249 a0001c0002t0007g0243 a0001c0002t0007g0245 others(1): Show |
4 | NA18989.hp2 NA19007.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+776_921+791dup others(16): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(13): Show |
1 | a0001c0002t0002g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.921+772_921+791dup others(20): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | G | GGTGTGTG others(15): Show |
1 | a0001c0002t0002g0244 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.921+770_921+791dup others(22): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724298 | GGT | G | 3 | a0001c0002t0011g0049 a0001c0003t0002g0098 a0002c0001t0001g0234 |
4 | HG02056.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+790_921+791del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | ||||||
| chr3:45724334 | T | TGTGTG | 3 | a0001c0002t0012g0120 a0002c0001t0001g0191 a0002c0001t0001g0235 |
3 | HG01515.hp2 NA18980.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.921+791_921+792ins others(5): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724334 | |||||||
| chr3:45724366 | G | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.921+823G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724366 | |||||||
| chr3:45724479 | C | T | 2 | a0001c0002t0004g0041 a0001c0002t0004g0172 |
3 | HG02257.hp1 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.921+936C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724479 | |||||||
| chr3:45724563 | C | T | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.921+1020C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724563 | |||||||
| chr3:45724730 | T | A | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.921+1187T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724730 | |||||||
| chr3:45725306 | T | TTGTC | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.921+1763_921+1764i others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725306 | |||||||
| chr3:45725328 | TTTTA | T | 10 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0122 others(7): Show |
14 | HG00140.hp1 HG00639.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.921+1795_921+1798d others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45725328 | ||||||
| chr3:45725526 | T | C | 1 | a0001c0003t0002g0083 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.921+1983T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725526 | |||||||
| chr3:45725581 | A | T | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+2038A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725581 | |||||||
| chr3:45725624 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.921+2081A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725624 | |||||||
| chr3:45725684 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.921+2141C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725684 | |||||||
| chr3:45725685 | T | C | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.921+2142T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725685 | |||||||
| chr3:45725696 | CT | C | 3 | a0001c0002t0002g0110 a0001c0002t0002g0111 a0001c0002t0002g0112 |
3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.921+2155delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45725696 | ||||||
| chr3:45725995 | G | A | 149 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(146): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.921+2452G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725995 | |||||||
| chr3:45726110 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.921+2567C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726110 | |||||||
| chr3:45726640 | T | C | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+3097T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726640 | |||||||
| chr3:45726791 | T | C | 1 | a0002c0001t0001g0068 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.921+3248T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726791 | |||||||
| chr3:45726859 | TGCTTTAT others(318): Show |
T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.921+3327_921+3651d others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45726859 | ||||||
| chr3:45726869 | C | CT | 21 | a0002c0001t0001g0001 a0002c0001t0001g0006 a0002c0001t0001g0026 others(18): Show |
21 | HG00423.hp2 HG00738.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.921+3353dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45726869 | ||||||
| chr3:45726869 | CT | C | 6 | a0002c0001t0001g0001 a0002c0001t0001g0030 a0002c0001t0001g0105 others(3): Show |
8 | HG01515.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+3353delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45726869 | ||||||
| chr3:45726873 | T | C | 1 | a0002c0001t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.921+3330T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726873 | |||||||
| chr3:45726902 | G | A | 1 | a0002c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.921+3359G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726902 | |||||||
| chr3:45726909 | C | T | 1 | a0002c0001t0001g0069 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.921+3366C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726909 | |||||||
| chr3:45726918 | A | G | 7 | a0002c0001t0001g0030 a0002c0001t0001g0077 a0002c0001t0001g0105 others(4): Show |
8 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+3375A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726918 | |||||||
| chr3:45726933 | C | T | 1 | a0002c0001t0001g0030 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.921+3390C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726933 | |||||||
| chr3:45727047 | G | A | 1 | a0002c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.921+3504G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727047 | |||||||
| chr3:45727165 | G | C | 1 | a0002c0001t0001g0030 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.921+3622G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727165 | |||||||
| chr3:45727245 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.921+3702A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727245 | |||||||
| chr3:45727341 | G | C | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.921+3798G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727341 | |||||||
| chr3:45727489 | G | A | 133 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(130): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.922-3812G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727489 | |||||||
| chr3:45727497 | C | T | 1 | a0002c0001t0001g0236 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.922-3804C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727497 | |||||||
| chr3:45727643 | G | A | 5 | a0001c0003t0002g0013 a0001c0003t0002g0095 a0001c0003t0002g0096 others(2): Show |
7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.922-3658G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727643 | |||||||
| chr3:45727675 | G | A | 1 | a0002c0001t0001g0030 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.922-3626G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727675 | |||||||
| chr3:45727740 | C | T | 2 | a0001c0003t0002g0007 a0001c0003t0002g0091 |
5 | HG01358.hp2 HG01943.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-3561C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727740 | |||||||
| chr3:45727797 | G | A | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.922-3504G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727797 | |||||||
| chr3:45727847 | G | A | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.922-3454G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727847 | |||||||
| chr3:45728171 | T | C | 1 | a0002c0001t0001g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.922-3130T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728171 | |||||||
| chr3:45728353 | G | T | 1 | a0002c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.922-2948G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728353 | |||||||
| chr3:45728563 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.922-2738G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728563 | |||||||
| chr3:45728595 | A | C | 64 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0015 others(61): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.922-2706A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728595 | |||||||
| chr3:45728812 | A | G | 1 | a0002c0001t0014g0055 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.922-2489A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728812 | |||||||
| chr3:45729038 | T | C | 1 | a0001c0002t0004g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.922-2263T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729038 | |||||||
| chr3:45729073 | G | GATTT | 26 | a0001c0002t0002g0004 a0001c0003t0002g0003 a0001c0003t0002g0007 others(23): Show |
41 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.922-2203_922-2200d others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45729073 | ||||||
| chr3:45729098 | A | T | 1 | a0002c0001t0001g0075 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.922-2203A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729098 | |||||||
| chr3:45729280 | T | A | 1 | a0001c0003t0002g0108 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.922-2021T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729280 | |||||||
| chr3:45729283 | T | TGC | 236 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(233): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.922-2018_922-2017i others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729283 | |||||||
| chr3:45729355 | G | T | 2 | a0001c0002t0002g0114 a0001c0002t0002g0115 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.922-1946G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729355 | |||||||
| chr3:45729708 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.922-1593C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729708 | |||||||
| chr3:45729730 | C | T | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.922-1571C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729730 | |||||||
| chr3:45729745 | G | A | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.922-1556G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729745 | |||||||
| chr3:45729904 | A | G | 1 | a0002c0001t0001g0217 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.922-1397A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729904 | |||||||
| chr3:45729981 | A | C | 1 | a0002c0001t0001g0225 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.922-1320A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729981 | |||||||
| chr3:45730109 | C | G | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.922-1192C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730109 | |||||||
| chr3:45730193 | C | T | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.922-1108C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730193 | |||||||
| chr3:45730296 | G | A | 8 | a0002c0001t0001g0024 a0002c0001t0001g0056 a0002c0001t0001g0057 others(5): Show |
9 | HG02055.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.922-1005G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730296 | |||||||
| chr3:45730307 | G | GT | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.922-986dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45730307 | ||||||
| chr3:45730307 | G | T | 1 | a0001c0004t0002g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.922-994G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730307 | |||||||
| chr3:45730349 | AT | A | 9 | a0001c0002t0005g0146 a0002c0001t0001g0030 a0002c0001t0001g0068 others(6): Show |
10 | HG01243.hp1 HG02630.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.922-938delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45730349 | ||||||
| chr3:45730349 | ATT | A | 140 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(137): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.922-939_922-938del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45730349 | ||||||
| chr3:45730736 | A | G | 21 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0015 others(18): Show |
32 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.922-565A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730736 | |||||||
| chr3:45730868 | G | A | 3 | a0001c0002t0002g0110 a0001c0002t0002g0111 a0001c0002t0002g0112 |
3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.922-433G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730868 | |||||||
| chr3:45731250 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.922-51T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731250 | |||||||
| chr3:45731252 | C | T | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.922-49C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731252 | |||||||
| chr3:45731280 | G | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.922-21G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731280 | |||||||
| chr3:45731295 | T | C | 1 | a0001c0003t0002g0089 | 1 | HG02004.hp1 | splice_region_variant&intron_variant | LOW | c.922-6T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731295 | |||||||
| chr3:45731496 | A | AGATCAAA others(12): Show |
1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1001+118_1001+136d others(21): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 45731496 | ||||||
| chr3:45731547 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001+167G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731547 | |||||||
| chr3:45731555 | A | G | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1001+175A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731555 | |||||||
| chr3:45731796 | A | C | 31 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(28): Show |
44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1002-257A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731796 | |||||||
| chr3:45731828 | A | C | 1 | a0002c0001t0001g0237 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1002-225A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731828 | |||||||
| chr3:45731828 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1002-225A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731828 | |||||||
| chr3:45731906 | G | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002-147G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731906 | |||||||
| chr3:45732047 | T | C | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | splice_region_variant&intron_variant | LOW | c.1002-6T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45732047 | |||||||
| chr3:45732049 | G | A | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | splice_region_variant&intron_variant | LOW | c.1002-4G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45732049 | |||||||
| chr3:45732158 | TATATTAT others(4): Show |
T | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | splice_region_variant&intron_variant | LOW | c.1100+8_1100+18delA others(10): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732158 | |||||||
| chr3:45732171 | T | A | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+20T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732171 | |||||||
| chr3:45732172 | A | G | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+21A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732172 | |||||||
| chr3:45732177 | G | T | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+26G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732177 | |||||||
| chr3:45732178 | G | A | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+27G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732178 | |||||||
| chr3:45732185 | G | C | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+34G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732185 | |||||||
| chr3:45732205 | C | A | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+54C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732205 | |||||||
| chr3:45732211 | T | A | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+60T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732211 | |||||||
| chr3:45732213 | A | C | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+62A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732213 | |||||||
| chr3:45732215 | T | A | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+64T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732215 | |||||||
| chr3:45732216 | A | T | 1 | a0002c0001t0001g0193 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+65A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732216 | |||||||
| chr3:45732240 | G | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1100+89G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732240 | |||||||
| chr3:45732257 | G | C | 1 | a0001c0002t0002g0244 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1100+106G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732257 | |||||||
| chr3:45732295 | C | A | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1100+144C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732295 | |||||||
| chr3:45732395 | T | A | 1 | a0002c0001t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1100+244T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732395 | |||||||
| chr3:45732471 | A | G | 12 | a0002c0001t0001g0006 a0002c0001t0001g0050 a0002c0001t0001g0065 others(9): Show |
16 | HG00609.hp2 HG01255.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100+320A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732471 | |||||||
| chr3:45732499 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1100+348C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732499 | |||||||
| chr3:45732616 | A | G | 1 | a0001c0002t0003g0156 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1100+465A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732616 | |||||||
| chr3:45732686 | T | A | 1 | a0002c0001t0001g0030 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100+535T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732686 | |||||||
| chr3:45733009 | C | G | 236 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(233): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1100+858C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733009 | |||||||
| chr3:45733204 | G | A | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1100+1053G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733204 | |||||||
| chr3:45733269 | G | T | 1 | a0002c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1100+1118G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733269 | |||||||
| chr3:45733508 | T | C | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1100+1357T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733508 | |||||||
| chr3:45733526 | G | A | 74 | a0002c0001t0001g0001 a0002c0001t0001g0005 a0002c0001t0001g0012 others(71): Show |
108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1100+1375G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733526 | |||||||
| chr3:45733699 | G | A | 1 | a0001c0002t0002g0244 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1101-1536G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733699 | |||||||
| chr3:45733747 | T | C | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1101-1488T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733747 | |||||||
| chr3:45733854 | C | T | 2 | a0002c0001t0001g0199 a0002c0001t0001g0240 |
2 | NA18991.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1101-1381C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733854 | |||||||
| chr3:45734014 | T | A | 5 | a0001c0002t0002g0033 a0001c0002t0002g0121 a0001c0002t0002g0125 others(2): Show |
6 | HG00738.hp1 HG01070.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1101-1221T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734014 | |||||||
| chr3:45734037 | G | A | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1101-1198G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734037 | |||||||
| chr3:45734113 | A | AT | 9 | a0002c0001t0001g0056 a0002c0001t0001g0187 a0002c0001t0001g0209 others(6): Show |
9 | HG01243.hp1 HG01261.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101-1105dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | ||||||
| chr3:45734113 | A | ATTC | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1101-1120_1101-111 others(7): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | ||||||
| chr3:45734113 | A | ATTT | 41 | a0001c0002t0002g0014 a0001c0002t0002g0032 a0001c0002t0002g0110 others(38): Show |
56 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.1101-1107_1101-110 others(7): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | ||||||
| chr3:45734113 | A | ATTTT | 87 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(84): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1101-1108_1101-110 others(8): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | ||||||
| chr3:45734136 | G | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1101-1099G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734136 | |||||||
| chr3:45734150 | C | T | 3 | a0001c0003t0002g0095 a0001c0003t0002g0096 a0001c0003t0002g0098 |
3 | HG02886.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1101-1085C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734150 | |||||||
| chr3:45734187 | C | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1101-1048C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734187 | |||||||
| chr3:45734386 | C | G | 1 | a0001c0002t0002g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1101-849C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734386 | |||||||
| chr3:45734412 | C | CA | 10 | a0001c0002t0006g0017 a0001c0002t0006g0148 a0001c0002t0013g0017 others(7): Show |
15 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.1101-813dupA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734412 | ||||||
| chr3:45734439 | A | T | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1101-796A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734439 | |||||||
| chr3:45734460 | A | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101-775A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734460 | |||||||
| chr3:45734620 | G | A | 1 | a0001c0002t0003g0157 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1101-615G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734620 | |||||||
| chr3:45734772 | A | G | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1101-463A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734772 | |||||||
| chr3:45735383 | C | CT | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1239+23dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr3 | 45735383 | ||||||
| chr3:45735408 | A | G | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1239+35A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735408 | |||||||
| chr3:45735567 | A | G | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1239+194A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735567 | |||||||
| chr3:45735621 | G | A | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1239+248G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735621 | |||||||
| chr3:45735949 | C | G | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239+576C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735949 | |||||||
| chr3:45736077 | C | T | 1 | a0002c0001t0001g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1239+704C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736077 | |||||||
| chr3:45736277 | A | G | 3 | a0001c0002t0005g0011 a0001c0002t0005g0159 a0001c0002t0005g0160 |
6 | NA18957.hp1 NA18994.hp2 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+904A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736277 | |||||||
| chr3:45736369 | A | G | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1239+996A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736369 | |||||||
| chr3:45736796 | C | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1240-787C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736796 | |||||||
| chr3:45736837 | C | G | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1240-746C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736837 | |||||||
| chr3:45736856 | A | G | 1 | a0002c0001t0001g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1240-727A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736856 | |||||||
| chr3:45736988 | G | A | 1 | a0002c0001t0001g0047 | 2 | NA18992.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1240-595G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736988 | |||||||
| chr3:45737057 | G | A | 1 | a0001c0002t0005g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1240-526G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737057 | |||||||
| chr3:45737131 | G | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1240-452G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737131 | |||||||
| chr3:45737169 | G | C | 3 | a0001c0002t0003g0038 a0001c0002t0003g0153 a0001c0002t0003g0165 |
4 | NA18946.hp1 NA18963.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-414G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737169 | |||||||
| chr3:45737176 | T | C | 1 | a0002c0001t0001g0211 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1240-407T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737176 | |||||||
| chr3:45737280 | G | A | 1 | a0002c0001t0001g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1240-303G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737280 | |||||||
| chr3:45737524 | C | G | 1 | a0002c0001t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1240-59C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737524 | |||||||
| chr3:45737953 | C | A | 1 | a0001c0002t0007g0245 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1382+109C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45737953 | |||||||
| chr3:45738101 | C | T | 1 | a0002c0001t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1382+257C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738101 | |||||||
| chr3:45738220 | A | G | 10 | a0002c0001t0001g0023 a0002c0001t0001g0024 a0002c0001t0001g0056 others(7): Show |
12 | HG01884.hp1 HG02055.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383-358A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738220 | |||||||
| chr3:45738451 | G | A | 149 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(146): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1383-127G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738451 | |||||||
| chr3:45738560 | T | C | 2 | a0002c0001t0001g0194 a0002c0001t0001g0225 |
2 | HG02155.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1383-18T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738560 | |||||||
| chr3:45738565 | C | T | 3 | a0002c0001t0001g0203 a0002c0001t0001g0207 a0002c0001t0001g0208 |
3 | NA18974.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1383-13C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738565 | |||||||
| chr3:45738700 | A | C | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1476+29A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 17/19 | chr3 | 45738700 | |||||||
| chr3:45738899 | A | G | 1 | a0002c0001t0001g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1569+26A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45738899 | |||||||
| chr3:45738954 | C | T | 1 | a0001c0003t0002g0100 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1569+81C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45738954 | |||||||
| chr3:45739049 | G | C | 1 | a0002c0001t0001g0205 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1569+176G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739049 | |||||||
| chr3:45739174 | A | G | 1 | a0002c0001t0001g0056 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1569+301A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739174 | |||||||
| chr3:45739288 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1570-299T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739288 | |||||||
| chr3:45739333 | A | T | 1 | a0001c0002t0002g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1570-254A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739333 | |||||||
| chr3:45739414 | A | G | 74 | a0002c0001t0001g0001 a0002c0001t0001g0005 a0002c0001t0001g0012 others(71): Show |
108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1570-173A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739414 | |||||||
| chr3:45739488 | A | G | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1570-99A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739488 | |||||||
| chr3:45739580 | T | C | 3 | a0002c0001t0001g0030 a0002c0001t0001g0105 a0002c0001t0001g0106 |
4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1570-7T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739580 | |||||||
| chr3:45739656 | C | T | 17 | a0001c0002t0002g0009 a0001c0002t0002g0014 a0001c0002t0002g0032 others(14): Show |
23 | HG00735.hp2 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1627+12C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739656 | |||||||
| chr3:45739696 | T | G | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1627+52T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739696 | |||||||
| chr3:45739724 | G | A | 1 | a0001c0002t0002g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1627+80G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739724 | |||||||
| chr3:45739878 | C | T | 1 | a0002c0001t0001g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1627+234C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739878 | |||||||
| chr3:45739888 | A | G | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1627+244A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739888 | |||||||
| chr3:45739981 | A | G | 4 | a0002c0001t0001g0199 a0002c0001t0001g0200 a0002c0001t0001g0214 others(1): Show |
4 | NA18991.hp1 NA18998.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+337A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739981 | |||||||
| chr3:45740003 | A | C | 1 | a0001c0002t0011g0049 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1627+359A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740003 | |||||||
| chr3:45740023 | C | T | 40 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(37): Show |
55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1627+379C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740023 | |||||||
| chr3:45740091 | G | C | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1627+447G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740091 | |||||||
| chr3:45740094 | A | C | 6 | a0001c0002t0003g0139 a0001c0002t0003g0151 a0001c0002t0003g0154 others(3): Show |
6 | HG00609.hp1 HG03017.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+450A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740094 | |||||||
| chr3:45740123 | T | C | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627+479T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740123 | |||||||
| chr3:45740163 | G | A | 1 | a0001c0002t0002g0036 | 2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1627+519G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740163 | |||||||
| chr3:45740606 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1627+962T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740606 | |||||||
| chr3:45740633 | A | C | 1 | a0002c0001t0001g0077 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627+989A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740633 | |||||||
| chr3:45741025 | A | G | 1 | a0001c0002t0005g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1627+1381A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741025 | |||||||
| chr3:45741094 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1627+1450G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741094 | |||||||
| chr3:45741174 | C | T | 3 | a0002c0001t0001g0180 a0002c0001t0001g0206 a0002c0001t0001g0239 |
3 | HG00733.hp1 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1627+1530C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741174 | |||||||
| chr3:45741262 | T | G | 1 | a0001c0003t0002g0108 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1627+1618T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741262 | |||||||
| chr3:45741271 | G | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1627+1627G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741271 | |||||||
| chr3:45741323 | A | T | 2 | a0002c0001t0001g0027 a0002c0001t0001g0075 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1627+1679A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741323 | |||||||
| chr3:45741652 | G | A | 10 | a0001c0002t0002g0021 a0001c0002t0002g0242 a0001c0002t0002g0244 others(7): Show |
11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1628-1881G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741652 | |||||||
| chr3:45741980 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1628-1553T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741980 | |||||||
| chr3:45742132 | C | T | 2 | a0002c0001t0009g0103 a0002c0001t0009g0104 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1628-1401C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742132 | |||||||
| chr3:45742316 | T | C | 13 | a0001c0002t0004g0018 a0001c0002t0004g0039 a0001c0002t0004g0040 others(10): Show |
19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1628-1217T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742316 | |||||||
| chr3:45742554 | C | G | 92 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(89): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1628-979C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742554 | |||||||
| chr3:45742590 | T | C | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1628-943T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742590 | |||||||
| chr3:45742787 | G | A | 1 | a0002c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1628-746G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742787 | |||||||
| chr3:45742792 | A | C | 1 | a0002c0001t0001g0068 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1628-741A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742792 | |||||||
| chr3:45742925 | T | C | 26 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0008 others(23): Show |
37 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1628-608T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742925 | |||||||
| chr3:45743093 | T | TA | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1628-438dupA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr3 | 45743093 | ||||||
| chr3:45743110 | G | A | 142 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(139): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1628-423G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743110 | |||||||
| chr3:45743262 | C | T | 9 | a0001c0003t0002g0022 a0001c0003t0002g0031 a0001c0003t0002g0051 others(6): Show |
11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1628-271C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743262 | |||||||
| chr3:45743471 | T | C | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1628-62T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743471 | |||||||
| chr3:45743480 | GGT | G | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1628-52_1628-51del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743480 |