Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29995 |
| ensemblid | ENSG00000071282.12 |
| hgncid | 6633 |
| symbol | LMCD1 |
| name | LIM and cysteine rich domains 1 |
| refseq_nuc | NM_014583.4 |
| refseq_prot | NP_055398.1 |
| ensembl_nuc | ENST00000157600.8 |
| ensembl_prot | ENSP00000157600.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 8501823 |
| end | 8574668 |
| strand | + |
| ver | v1.2 |
| region | chr3:8501823-8574668 |
| region5000 | chr3:8496823-8579668 |
| regionname0 | LMCD1_chr3_8501823_8574668 |
| regionname5000 | LMCD1_chr3_8496823_8579668 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 365 | 304 | 78 | 63 | 110 | 14 | 37 | 76 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0002 | 0/0 | 365 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0003 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0004 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0005 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0006 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0007 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0008 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0009 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| a0010 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | MAKVA others(360): Show |
chr3 | 8496823 | 8579668 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1095 | 266 | 67 | 56 | 102 | 13 | 27 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0001c0002 | 0/1 | 1095 | 36 | 10 | 7 | 8 | 1 | 9 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0001c0008 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0001c0013 | 0/0 | 1095 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0002c0003 | 0/0 | 1095 | 2 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0003c0010 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0004c0011 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0005c0007 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0006c0006 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0007c0012 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0008c0009 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0009c0005 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 | ||
| a0010c0004 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | ATGGC others(1090): Show |
chr3 | 8496823 | 8579668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8286 | 66 | 21 | 18 | 20 | 5 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0002 | 1/0 | 8284 | 64 | 14 | 13 | 25 | 2 | 9 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0003 | 0/0 | 8285 | 64 | 3 | 19 | 29 | 5 | 8 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0004 | 0/0 | 8284 | 10 | 5 | 0 | 0 | 0 | 5 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0005 | 0/0 | 8284 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0006 | 0/0 | 8286 | 4 | 0 | 0 | 4 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0007 | 0/0 | 8287 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8282): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0009 | 0/0 | 8285 | 3 | 1 | 1 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0010 | 0/0 | 8283 | 3 | 0 | 0 | 3 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8278): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0012 | 0/0 | 8269 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8264): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0013 | 0/0 | 8286 | 2 | 1 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0014 | 0/0 | 8284 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0015 | 0/0 | 8284 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0016 | 0/0 | 8283 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8278): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0017 | 0/0 | 8287 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8282): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0018 | 0/0 | 8285 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0020 | 0/0 | 8284 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0021 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0022 | 0/0 | 8287 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8282): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0023 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0024 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0026 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0027 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0028 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0029 | 0/0 | 8286 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0030 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0031 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0032 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0033 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0034 | 0/0 | 8287 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8282): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0035 | 0/0 | 8286 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0036 | 0/0 | 8286 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0037 | 0/0 | 8287 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8282): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0038 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0039 | 0/0 | 8287 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8282): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0040 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0042 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0043 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0044 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8278): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0045 | 0/0 | 8285 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0046 | 0/0 | 8285 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0047 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0048 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0049 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0051 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0052 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0053 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0001t0055 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0001 | 0/0 | 8286 | 11 | 2 | 6 | 0 | 0 | 3 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0002 | 0/0 | 8284 | 4 | 1 | 1 | 0 | 0 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0003 | 0/1 | 8285 | 6 | 0 | 0 | 2 | 1 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0004 | 0/0 | 8284 | 3 | 2 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0005 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0008 | 0/0 | 8284 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0011 | 0/0 | 8285 | 3 | 0 | 0 | 3 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0019 | 0/0 | 8285 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0041 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0050 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0054 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0002t0056 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0001c0008t0002 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0001c0013t0019 | 0/0 | 8285 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0002c0003t0001 | 0/0 | 8286 | 2 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0003c0010t0002 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0004c0011t0001 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0005c0007t0025 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0006c0006t0001 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0007c0012t0001 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| a0008c0009t0002 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8279): Show |
chr3 | 8496823 | 8579668 |
| a0009c0005t0003 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8280): Show |
chr3 | 8496823 | 8579668 |
| a0010c0004t0001 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | GCACA others(8281): Show |
chr3 | 8496823 | 8579668 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0004 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0010g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0012g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0013g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0014g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0016g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0017g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0018g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0018g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0020g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0021g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0022g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0023g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0024g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0026g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0027g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0028g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0029g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0030g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0031g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0032g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0033g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0034g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0035g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0036g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0038g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0039g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0040g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0042g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0043g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0044g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0045g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0046g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0047g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0048g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0049g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0051g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0052g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0053g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0055g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0011g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0011g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0019g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0041g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0050g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0054g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0056g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0008t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0013t0019g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0003c0010t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0004c0011t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0005c0007t0025g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0006c0006t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0007c0012t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0008c0009t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0009c0005t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0010c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0168 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00323 | hp1 | a0001 | c0001 | t0039 | g0268 | EUR | FIN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0052 | EUR | FIN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00408 | hp1 | a0001 | c0001 | t0032 | g0134 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00423 | hp1 | a0001 | c0002 | t0054 | g0029 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0112 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00597 | hp2 | a0001 | c0001 | t0044 | g0242 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00609 | hp1 | a0001 | c0001 | t0018 | g0148 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00738 | hp1 | a0001 | c0001 | t0055 | g0034 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01074 | hp2 | a0001 | c0001 | t0029 | g0289 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01099 | hp1 | a0001 | c0001 | t0036 | g0243 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0042 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0298 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01192 | hp2 | a0001 | c0001 | t0049 | g0285 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0284 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01884 | hp2 | a0001 | c0001 | t0052 | g0295 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0101 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02015 | hp1 | a0001 | c0001 | t0051 | g0108 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02015 | hp2 | a0001 | c0001 | t0030 | g0163 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0296 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02080 | hp1 | a0001 | c0001 | t0038 | g0143 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0115 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0118 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02258 | hp1 | a0001 | c0002 | t0008 | g0195 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02280 | hp1 | a0001 | c0002 | t0008 | g0194 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02451 | hp1 | a0001 | c0001 | t0047 | g0276 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02451 | hp2 | a0001 | c0002 | t0050 | g0193 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02523 | hp1 | a0001 | c0001 | t0017 | g0230 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02572 | hp2 | a0001 | c0001 | t0053 | g0269 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02615 | hp1 | a0001 | c0001 | t0040 | g0205 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02615 | hp2 | a0001 | c0001 | t0022 | g0279 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0237 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02717 | hp1 | a0001 | c0001 | t0031 | g0082 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0188 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0222 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0196 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0077 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02896 | hp1 | a0003 | c0010 | t0002 | g0119 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0225 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02965 | hp2 | a0004 | c0011 | t0001 | g0254 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02976 | hp2 | a0001 | c0001 | t0034 | g0238 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0028 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03041 | hp1 | a0005 | c0007 | t0025 | g0203 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03098 | hp2 | a0001 | c0001 | t0043 | g0015 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0211 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0270 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0240 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03225 | hp2 | a0001 | c0008 | t0002 | g0081 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03491 | hp2 | a0001 | c0001 | t0020 | g0020 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0297 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0080 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03669 | hp1 | a0001 | c0002 | t0019 | g0074 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03669 | hp2 | a0001 | c0013 | t0019 | g0145 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03688 | hp1 | a0001 | c0001 | t0035 | g0247 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0236 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0084 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0149 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04115 | hp2 | a0001 | c0001 | t0045 | g0057 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18522 | hp1 | a0006 | c0006 | t0001 | g0228 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0172 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18612 | hp2 | a0007 | c0012 | t0001 | g0099 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18747 | hp1 | a0008 | c0009 | t0002 | g0071 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18939 | hp1 | a0001 | c0002 | t0011 | g0026 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18950 | hp2 | a0001 | c0002 | t0041 | g0256 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18956 | hp1 | a0001 | c0001 | t0017 | g0229 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18965 | hp1 | a0001 | c0001 | t0028 | g0176 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0091 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18969 | hp2 | a0009 | c0005 | t0003 | g0109 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18974 | hp2 | a0001 | c0001 | t0027 | g0092 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18979 | hp1 | a0001 | c0001 | t0033 | g0133 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18981 | hp1 | a0001 | c0002 | t0011 | g0027 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18984 | hp2 | a0001 | c0002 | t0056 | g0073 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18990 | hp2 | a0001 | c0001 | t0024 | g0129 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18992 | hp1 | a0001 | c0001 | t0016 | g0180 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18995 | hp2 | a0001 | c0001 | t0042 | g0223 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18999 | hp2 | a0001 | c0001 | t0026 | g0064 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19005 | hp1 | a0001 | c0002 | t0011 | g0019 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19012 | hp2 | a0001 | c0001 | t0016 | g0060 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19057 | hp1 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19063 | hp1 | a0010 | c0004 | t0001 | g0114 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19075 | hp1 | a0001 | c0001 | t0048 | g0096 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19080 | hp1 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19086 | hp1 | a0001 | c0001 | t0018 | g0130 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0083 | AFR | ASW | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | TSI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0282 | EUR | TSI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | GIH | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | GIH | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02109 | hp1 | a0001 | c0002 | t0008 | g0185 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0078 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0248 | AFR | USA | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA21309 | hp1 | a0001 | c0001 | t0046 | g0204 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0300 | REF | REF | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0004 | REF | REF | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8537406 | A | G | 1 | a0007 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.353A>G | p.Tyr118Cys | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/6 | 469/8284 | 353/1098 | 118/365 | chr3 | 8537406 | |||
| chr3:8548610 | G | A | 1 | a0010 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.430G>A | p.Val144Met | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 546/8284 | 430/1098 | 144/365 | chr3 | 8548610 | |||
| chr3:8548781 | C | T | 1 | a0006 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.601C>T | p.Leu201Phe | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 717/8284 | 601/1098 | 201/365 | chr3 | 8548781 | |||
| chr3:8548854 | C | T | 1 | a0004 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.674C>T | p.Ala225Val | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 790/8284 | 674/1098 | 225/365 | chr3 | 8548854 | |||
| chr3:8565558 | G | A | 1 | a0009 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.850G>A | p.Asp284Asn | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/6 | 966/8284 | 850/1098 | 284/365 | chr3 | 8565558 | |||
| chr3:8565597 | G | T | 1 | a0003 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.889G>T | p.Gly297Cys | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/6 | 1005/8284 | 889/1098 | 297/365 | chr3 | 8565597 | |||
| chr3:8565621 | C | T | 1 | a0002 | 2 | HG01106.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.913C>T | p.Arg305Trp | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/6 | 1029/8284 | 913/1098 | 305/365 | chr3 | 8565621 | |||
| chr3:8567500 | G | A | 1 | a0005 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1000G>A | p.Val334Ile | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1116/8284 | 1000/1098 | 334/365 | chr3 | 8567500 | |||
| chr3:8567591 | G | A | 1 | a0008 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1091G>A | p.Arg364His | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1207/8284 | 1091/1098 | 364/365 | chr3 | 8567591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8537314 | C | T | 1 | a0001c0013 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.261C>T | p.Gly87Gly | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/6 | 377/8284 | 261/1098 | 87/365 | chr3 | 8537314 | |||
| chr3:8548627 | T | C | 3 | a0001c0002 a0006c0006 a0009c0005 |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
synonymous_variant | LOW | c.447T>C | p.Gly149Gly | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 563/8284 | 447/1098 | 149/365 | chr3 | 8548627 | |||
| chr3:8567538 | G | A | 1 | a0001c0008 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1038G>A | p.Ala346Ala | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1154/8284 | 1038/1098 | 346/365 | chr3 | 8567538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8501842 | G | T | 2 | a0001c0002t0011 a0001c0002t0056 |
4 | NA18939.hp1 NA18981.hp1 NA18984.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/6 | 97 | chr3 | 8501842 | ||||||
| chr3:8501915 | G | A | 1 | a0001c0001t0020 | 1 | HG03491.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/6 | 24 | chr3 | 8501915 | ||||||
| chr3:8567682 | T | C | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0021 others(1): Show |
7 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*84T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 84 | chr3 | 8567682 | ||||||
| chr3:8567895 | G | A | 1 | a0001c0001t0023 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 297 | chr3 | 8567895 | ||||||
| chr3:8567939 | C | T | 1 | a0001c0001t0055 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 341 | chr3 | 8567939 | ||||||
| chr3:8567940 | G | A | 1 | a0001c0002t0008 | 3 | HG02109.hp1 HG02258.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*342G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 342 | chr3 | 8567940 | ||||||
| chr3:8568085 | A | G | 2 | a0001c0001t0007 a0001c0001t0022 |
4 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*487A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 487 | chr3 | 8568085 | ||||||
| chr3:8568270 | G | A | 1 | a0001c0001t0024 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 672 | chr3 | 8568270 | ||||||
| chr3:8568364 | T | C | 1 | a0001c0001t0013 | 2 | HG01109.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*766T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 766 | chr3 | 8568364 | ||||||
| chr3:8568425 | T | C | 2 | a0001c0002t0008 a0005c0007t0025 |
4 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*827T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 827 | chr3 | 8568425 | ||||||
| chr3:8568548 | T | C | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | NA18974.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 950 | chr3 | 8568548 | ||||||
| chr3:8568895 | C | T | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(20): Show |
104 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1297C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1297 | chr3 | 8568895 | ||||||
| chr3:8569128 | A | G | 1 | a0001c0002t0054 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1530 | chr3 | 8569128 | ||||||
| chr3:8569250 | C | G | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(22): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1652C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1652 | chr3 | 8569250 | ||||||
| chr3:8569384 | A | G | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(21): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1786A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1786 | chr3 | 8569384 | ||||||
| chr3:8569445 | A | G | 1 | a0001c0001t0031 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1847A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1847 | chr3 | 8569445 | ||||||
| chr3:8569446 | C | T | 1 | a0001c0001t0053 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1848C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1848 | chr3 | 8569446 | ||||||
| chr3:8569505 | T | C | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1907T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1907 | chr3 | 8569505 | ||||||
| chr3:8569658 | G | C | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(19): Show |
103 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2060G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2060 | chr3 | 8569658 | ||||||
| chr3:8569767 | G | A | 2 | a0001c0001t0007 a0001c0001t0022 |
4 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2169G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2169 | chr3 | 8569767 | ||||||
| chr3:8569980 | C | CA | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(20): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2397dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2398 | INFO_REALIGN_3_PRIME | chr3 | 8569980 | |||||
| chr3:8569980 | C | CAA | 3 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0029 |
6 | HG01074.hp2 HG01975.hp2 HG02129.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2396_*2397dupAA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2398 | INFO_REALIGN_3_PRIME | chr3 | 8569980 | |||||
| chr3:8569980 | C | CAAA | 26 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(23): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2395_*2397dupAAA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2398 | INFO_REALIGN_3_PRIME | chr3 | 8569980 | |||||
| chr3:8570400 | G | T | 52 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(49): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*2802G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2802 | chr3 | 8570400 | ||||||
| chr3:8570412 | CA | C | 5 | a0001c0001t0004 a0001c0001t0052 a0001c0001t0053 others(2): Show |
16 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2815delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2815 | chr3 | 8570412 | ||||||
| chr3:8570596 | G | C | 56 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(53): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2998G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2998 | chr3 | 8570596 | ||||||
| chr3:8570643 | C | T | 1 | a0001c0001t0030 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3045C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3045 | chr3 | 8570643 | ||||||
| chr3:8570666 | C | T | 1 | a0001c0001t0043 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3068C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3068 | chr3 | 8570666 | ||||||
| chr3:8570679 | T | G | 1 | a0001c0001t0014 | 2 | HG02055.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3081T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3081 | chr3 | 8570679 | ||||||
| chr3:8570715 | C | G | 1 | a0001c0001t0049 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3117C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3117 | chr3 | 8570715 | ||||||
| chr3:8570890 | G | A | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(48): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*3292G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3292 | chr3 | 8570890 | ||||||
| chr3:8571005 | G | C | 1 | a0001c0001t0030 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3407 | chr3 | 8571005 | ||||||
| chr3:8571017 | G | T | 24 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(21): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*3419G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3419 | chr3 | 8571017 | ||||||
| chr3:8571044 | G | A | 1 | a0001c0002t0056 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3446G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3446 | chr3 | 8571044 | ||||||
| chr3:8571061 | A | T | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3463A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3463 | chr3 | 8571061 | ||||||
| chr3:8571062 | TGTCAGCA others(9): Show |
T | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3466_*3481delTCAG others(12): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3466 | INFO_REALIGN_3_PRIME | chr3 | 8571062 | |||||
| chr3:8571079 | G | C | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3481G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3481 | chr3 | 8571079 | ||||||
| chr3:8571247 | A | G | 1 | a0001c0001t0042 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3649A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3649 | chr3 | 8571247 | ||||||
| chr3:8571515 | G | C | 1 | a0001c0001t0017 | 2 | HG02523.hp1 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3917G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3917 | chr3 | 8571515 | ||||||
| chr3:8571593 | C | G | 53 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(50): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*3995C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3995 | chr3 | 8571593 | ||||||
| chr3:8571674 | C | T | 1 | a0001c0002t0041 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4076C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4076 | chr3 | 8571674 | ||||||
| chr3:8571771 | C | G | 2 | a0001c0001t0006 a0001c0001t0044 |
5 | HG00597.hp2 HG02165.hp2 NA18992.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4173C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4173 | chr3 | 8571771 | ||||||
| chr3:8571782 | T | G | 1 | a0001c0002t0050 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4184T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4184 | chr3 | 8571782 | ||||||
| chr3:8571810 | G | A | 1 | a0001c0001t0014 | 2 | HG02055.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4212G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4212 | chr3 | 8571810 | ||||||
| chr3:8571813 | A | C | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(21): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*4215A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4215 | chr3 | 8571813 | ||||||
| chr3:8571820 | A | G | 2 | a0001c0001t0006 a0001c0001t0044 |
5 | HG00597.hp2 HG02165.hp2 NA18992.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4222A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4222 | chr3 | 8571820 | ||||||
| chr3:8571862 | A | T | 1 | a0001c0001t0040 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4264A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4264 | chr3 | 8571862 | ||||||
| chr3:8571863 | A | G | 3 | a0001c0001t0040 a0001c0002t0008 a0005c0007t0025 |
5 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4265A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4265 | chr3 | 8571863 | ||||||
| chr3:8571889 | G | A | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(22): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4291G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4291 | chr3 | 8571889 | ||||||
| chr3:8571978 | A | G | 2 | a0001c0001t0021 a0001c0001t0029 |
2 | HG01074.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4380A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4380 | chr3 | 8571978 | ||||||
| chr3:8572158 | A | G | 49 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(46): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*4560A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4560 | chr3 | 8572158 | ||||||
| chr3:8572453 | T | G | 3 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0022 |
6 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4855T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4855 | chr3 | 8572453 | ||||||
| chr3:8572537 | T | C | 1 | a0001c0001t0035 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4939T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4939 | chr3 | 8572537 | ||||||
| chr3:8572649 | T | C | 2 | a0001c0001t0021 a0001c0001t0029 |
2 | HG01074.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5051T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5051 | chr3 | 8572649 | ||||||
| chr3:8572694 | A | G | 1 | a0001c0001t0039 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5096A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5096 | chr3 | 8572694 | ||||||
| chr3:8572759 | T | C | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(22): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*5161T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5161 | chr3 | 8572759 | ||||||
| chr3:8572816 | G | A | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5218G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5218 | chr3 | 8572816 | ||||||
| chr3:8572856 | G | T | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(17): Show |
101 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5258G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5258 | chr3 | 8572856 | ||||||
| chr3:8573188 | T | C | 1 | a0001c0001t0014 | 2 | HG02055.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5590T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5590 | chr3 | 8573188 | ||||||
| chr3:8573309 | G | A | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(20): Show |
104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*5711G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5711 | chr3 | 8573309 | ||||||
| chr3:8573325 | G | A | 1 | a0001c0001t0017 | 2 | HG02523.hp1 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5727G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5727 | chr3 | 8573325 | ||||||
| chr3:8573372 | T | C | 1 | a0001c0001t0022 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5774T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5774 | chr3 | 8573372 | ||||||
| chr3:8573376 | T | C | 2 | a0001c0001t0005 a0001c0002t0005 |
4 | HG02622.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5778T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5778 | chr3 | 8573376 | ||||||
| chr3:8573421 | C | G | 1 | a0001c0001t0027 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5823C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5823 | chr3 | 8573421 | ||||||
| chr3:8573475 | G | A | 1 | a0001c0001t0046 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5877G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5877 | chr3 | 8573475 | ||||||
| chr3:8573521 | G | A | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(21): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*5923G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5923 | chr3 | 8573521 | ||||||
| chr3:8573528 | G | A | 1 | a0001c0001t0036 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5930G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5930 | chr3 | 8573528 | ||||||
| chr3:8573591 | G | A | 49 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(46): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5993G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5993 | chr3 | 8573591 | ||||||
| chr3:8573803 | A | G | 49 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(46): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*6205A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6205 | chr3 | 8573803 | ||||||
| chr3:8573876 | TA | T | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(24): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*6292delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6292 | INFO_REALIGN_3_PRIME | chr3 | 8573876 | |||||
| chr3:8573958 | G | A | 1 | a0001c0001t0038 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6360G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6360 | chr3 | 8573958 | ||||||
| chr3:8574184 | C | T | 1 | a0001c0001t0034 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6586C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6586 | chr3 | 8574184 | ||||||
| chr3:8574259 | A | G | 3 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0022 |
5 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6661A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6661 | chr3 | 8574259 | ||||||
| chr3:8574441 | C | A | 1 | a0001c0001t0015 | 2 | HG02622.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6843C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6843 | chr3 | 8574441 | ||||||
| chr3:8574442 | T | C | 50 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(47): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*6844T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6844 | chr3 | 8574442 | ||||||
| chr3:8574461 | G | T | 2 | a0001c0002t0019 a0001c0013t0019 |
2 | HG03669.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6863G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6863 | chr3 | 8574461 | ||||||
| chr3:8574577 | C | T | 1 | a0001c0001t0018 | 2 | HG00609.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6979C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6979 | chr3 | 8574577 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8502032 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42+52C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502032 | |||||||
| chr3:8502071 | A | C | 64 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0255 others(61): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.42+91A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502071 | |||||||
| chr3:8502076 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+96G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502076 | |||||||
| chr3:8502177 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+197T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502177 | |||||||
| chr3:8502206 | G | T | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+226G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502206 | |||||||
| chr3:8502269 | ATATATAT others(111): Show |
A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+316_42+433del | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502269 | ||||||
| chr3:8502270 | T | TATATATT others(82): Show |
6 | a0001c0001t0001g0217 a0001c0001t0002g0221 a0001c0001t0003g0213 others(3): Show |
6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+296_42+297insTT others(87): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502270 | ||||||
| chr3:8502278 | A | ATATATAT others(54): Show |
1 | a0001c0001t0002g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.42+298_42+299insTA others(59): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502278 | |||||||
| chr3:8502278 | A | T | 6 | a0001c0001t0001g0217 a0001c0001t0002g0221 a0001c0001t0003g0213 others(3): Show |
6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+298A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502278 | |||||||
| chr3:8502279 | A | T | 6 | a0001c0001t0001g0217 a0001c0001t0002g0221 a0001c0001t0003g0213 others(3): Show |
6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+299A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502279 | |||||||
| chr3:8502287 | T | A | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+307T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502287 | |||||||
| chr3:8502288 | A | T | 8 | a0001c0001t0001g0217 a0001c0001t0002g0097 a0001c0001t0002g0221 others(5): Show |
8 | HG00438.hp2 HG01243.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+308A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502288 | |||||||
| chr3:8502296 | T | A | 1 | a0001c0001t0002g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.42+316T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502296 | |||||||
| chr3:8502296 | T | TTTTA | 6 | a0001c0001t0001g0217 a0001c0001t0002g0221 a0001c0001t0003g0213 others(3): Show |
6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+317_42+318insTT others(2): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502296 | ||||||
| chr3:8502296 | TTATATAT others(11): Show |
T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0005g0192 others(1): Show |
4 | HG02976.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+324_42+341delAA others(16): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502296 | ||||||
| chr3:8502297 | T | A | 3 | a0001c0001t0002g0097 a0001c0002t0002g0236 a0001c0002t0002g0237 |
3 | HG01928.hp1 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+317T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502297 | |||||||
| chr3:8502297 | TATATATA others(9): Show |
T | 3 | a0001c0002t0001g0197 a0001c0002t0005g0196 a0006c0006t0001g0228 |
3 | HG02818.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.42+325_42+340delAT others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502297 | ||||||
| chr3:8502305 | A | T | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+325A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502305 | |||||||
| chr3:8502306 | T | A | 64 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0255 others(61): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.42+326T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502306 | |||||||
| chr3:8502312 | A | T | 92 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0217 others(89): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.42+332A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502312 | |||||||
| chr3:8502313 | A | AATATATA others(63): Show |
1 | a0001c0001t0002g0121 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.42+349_42+350insTA others(68): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | ||||||
| chr3:8502313 | A | AATATATA others(65): Show |
1 | a0002c0003t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.42+349_42+350insTA others(70): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | ||||||
| chr3:8502313 | A | AATATATA others(65): Show |
167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0023 others(164): Show |
171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(70): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | ||||||
| chr3:8502313 | A | AATATATA others(90): Show |
1 | a0001c0001t0003g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.42+349_42+350insTA others(95): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | ||||||
| chr3:8502313 | A | AATATATA others(81): Show |
8 | a0001c0001t0002g0009 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
9 | HG00438.hp1 HG00609.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(86): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | ||||||
| chr3:8502313 | A | T | 7 | a0001c0001t0001g0217 a0001c0001t0002g0097 a0001c0001t0002g0221 others(4): Show |
7 | HG00438.hp2 HG01243.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+333A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502313 | |||||||
| chr3:8502314 | A | T | 1 | a0001c0001t0022g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.42+334A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502314 | |||||||
| chr3:8502320 | A | ATTATATA others(2): Show |
19 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0299 others(16): Show |
19 | HG00423.hp1 HG02109.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.42+348_42+349insTT others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502320 | ||||||
| chr3:8502321 | T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0008 a0001c0001t0003g0207 a0001c0001t0003g0208 |
4 | HG01243.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(20): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502321 | ||||||
| chr3:8502322 | T | TATATAAA others(167): Show |
3 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0281 |
3 | HG02572.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42+347_42+348insAA others(172): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATAAA others(171): Show |
1 | a0001c0001t0005g0239 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+347_42+348insAA others(176): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATAAA others(194): Show |
1 | a0001c0002t0001g0244 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.42+347_42+348insAA others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATAAA others(169): Show |
47 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0255 others(44): Show |
50 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.42+347_42+348insAA others(174): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATAAA others(196): Show |
2 | a0001c0001t0002g0277 a0001c0001t0002g0278 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.42+347_42+348insAA others(201): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATATA others(144): Show |
1 | a0001c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.42+350_42+351insAA others(149): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATATA others(240): Show |
1 | a0001c0001t0001g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.42+350_42+351insAA others(245): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATATA others(194): Show |
2 | a0001c0001t0001g0262 a0001c0001t0001g0265 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.42+350_42+351insAA others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATATA others(169): Show |
2 | a0001c0001t0007g0240 a0001c0001t0022g0279 |
2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.42+357_42+358insAA others(174): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATATA others(169): Show |
1 | a0001c0001t0007g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.42+357_42+358insAA others(174): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502322 | T | TATATATA others(40): Show |
1 | a0001c0001t0012g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42+349_42+350insTA others(45): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | ||||||
| chr3:8502323 | A | ATATATAT others(65): Show |
3 | a0001c0001t0024g0129 a0001c0002t0001g0006 a0001c0002t0001g0079 |
4 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(70): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502323 | ||||||
| chr3:8502323 | A | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0005g0192 others(4): Show |
7 | HG02818.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+343A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502323 | |||||||
| chr3:8502328 | T | A | 2 | a0001c0001t0014g0296 a0001c0001t0052g0295 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.42+348T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502328 | |||||||
| chr3:8502328 | T | G | 2 | a0001c0001t0005g0239 a0001c0001t0012g0248 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.42+348T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502328 | |||||||
| chr3:8502328 | T | TATAA | 8 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0003g0138 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(2): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502328 | ||||||
| chr3:8502329 | A | ATAAAATA others(29): Show |
1 | a0001c0001t0003g0233 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+349_42+350insTA others(34): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502329 | |||||||
| chr3:8502335 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.42+355T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502335 | |||||||
| chr3:8502337 | T | A | 2 | a0001c0001t0001g0235 a0001c0001t0003g0233 |
2 | NA18943.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.42+357T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502337 | |||||||
| chr3:8502337 | T | TAATATAT others(159): Show |
1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+357_42+358insAA others(164): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502337 | |||||||
| chr3:8502338 | T | A | 12 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0003g0138 others(9): Show |
12 | HG00140.hp1 HG00639.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+358T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502338 | |||||||
| chr3:8502339 | A | ATATATAT others(194): Show |
2 | a0001c0001t0014g0296 a0001c0001t0052g0295 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.42+365_42+366insTT others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502339 | ||||||
| chr3:8502339 | A | T | 1 | a0001c0001t0003g0233 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+359A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502339 | |||||||
| chr3:8502346 | A | T | 11 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0003g0138 others(8): Show |
11 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+366A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502346 | |||||||
| chr3:8502347 | A | T | 3 | a0001c0001t0001g0235 a0001c0002t0001g0197 a0001c0002t0005g0196 |
3 | HG02818.hp1 NA18984.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.42+367A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502347 | |||||||
| chr3:8502348 | A | T | 2 | a0001c0002t0001g0197 a0001c0002t0005g0196 |
2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.42+368A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502348 | |||||||
| chr3:8502355 | A | T | 8 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0003g0138 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+375A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502355 | |||||||
| chr3:8502362 | T | TAAAATAT others(90): Show |
7 | a0001c0001t0001g0231 a0001c0001t0003g0138 a0001c0001t0003g0159 others(4): Show |
7 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+382_42+383insAA others(95): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502362 | |||||||
| chr3:8502362 | T | TTATATAA others(45): Show |
1 | a0001c0002t0004g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42+397_42+398insAT others(50): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | ||||||
| chr3:8502362 | T | TTATATAA others(120): Show |
2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+424_42+425insAT others(125): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | ||||||
| chr3:8502362 | T | TTATATAT others(97): Show |
17 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0299 others(14): Show |
17 | HG00423.hp1 HG02622.hp1 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+388_42+389insTA others(102): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | ||||||
| chr3:8502362 | T | TTATATAT others(122): Show |
1 | a0001c0001t0002g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42+388_42+389insTT others(127): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | ||||||
| chr3:8502363 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+383T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502363 | |||||||
| chr3:8502365 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+385T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502365 | |||||||
| chr3:8502368 | A | ATTCATAT others(5): Show |
1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+388_42+389insTT others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502368 | |||||||
| chr3:8502369 | A | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0003g0187 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+389A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502369 | |||||||
| chr3:8502370 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+390A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502370 | |||||||
| chr3:8502370 | AAT | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0257 a0001c0001t0005g0192 others(1): Show |
4 | HG02976.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+398_42+399delTA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502370 | ||||||
| chr3:8502372 | T | TATATATA others(194): Show |
1 | a0001c0002t0001g0002 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.42+424_42+425insAT others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502372 | ||||||
| chr3:8502397 | A | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.42+417A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502397 | |||||||
| chr3:8502408 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+428T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502408 | |||||||
| chr3:8502410 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+430T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502410 | |||||||
| chr3:8502411 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+431A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502411 | |||||||
| chr3:8502413 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+433A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502413 | |||||||
| chr3:8502569 | T | TAC | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0003g0021 others(3): Show |
6 | HG02698.hp2 HG03491.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+626_42+627dupAC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | ||||||
| chr3:8502569 | TAC | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0086 others(124): Show |
133 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.42+626_42+627delAC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | ||||||
| chr3:8502569 | TACAC | T | 40 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0186 others(37): Show |
40 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.42+624_42+627delAC others(2): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | ||||||
| chr3:8502569 | TACACAC | T | 12 | a0001c0001t0001g0224 a0001c0001t0001g0231 a0001c0001t0002g0227 others(9): Show |
12 | HG02155.hp1 HG02258.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+622_42+627delAC others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | ||||||
| chr3:8502569 | TACACACA others(11): Show |
T | 1 | a0001c0001t0005g0239 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+610_42+627delAC others(16): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | ||||||
| chr3:8502569 | TACACACA others(13): Show |
T | 62 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0255 others(59): Show |
66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.42+608_42+627delAC others(18): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | ||||||
| chr3:8502606 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0005g0192 others(3): Show |
6 | HG02818.hp1 HG02976.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+626A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502606 | |||||||
| chr3:8502606 | ACG | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0003g0048 |
4 | HG01256.hp1 HG01934.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+628_42+629delGC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502606 | ||||||
| chr3:8502608 | G | A | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+628G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502608 | |||||||
| chr3:8502630 | G | T | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+650G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502630 | |||||||
| chr3:8502734 | T | C | 70 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0255 others(67): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.42+754T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502734 | |||||||
| chr3:8502817 | G | T | 69 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0155 others(66): Show |
70 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.42+837G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502817 | |||||||
| chr3:8502850 | G | A | 1 | a0001c0001t0007g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42+870G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502850 | |||||||
| chr3:8502876 | G | A | 1 | a0001c0002t0008g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.42+896G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502876 | |||||||
| chr3:8502902 | C | T | 5 | a0001c0001t0002g0181 a0001c0001t0002g0183 a0001c0001t0002g0184 others(2): Show |
5 | HG00673.hp2 NA18943.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+922C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502902 | |||||||
| chr3:8502992 | C | G | 1 | a0006c0006t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.42+1012C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502992 | |||||||
| chr3:8503061 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42+1081C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503061 | |||||||
| chr3:8503214 | A | G | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+1234A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503214 | |||||||
| chr3:8503645 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0003g0187 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+1665G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503645 | |||||||
| chr3:8503777 | C | G | 1 | a0001c0001t0002g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.42+1797C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503777 | |||||||
| chr3:8503792 | C | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0299 others(14): Show |
17 | HG00423.hp1 HG02622.hp1 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+1812C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503792 | |||||||
| chr3:8503843 | T | C | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+1863T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503843 | |||||||
| chr3:8504081 | A | G | 1 | a0001c0001t0003g0010 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.42+2101A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504081 | |||||||
| chr3:8504114 | T | A | 61 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0255 others(58): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.42+2134T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504114 | |||||||
| chr3:8504204 | G | A | 2 | a0001c0001t0002g0135 a0001c0002t0004g0078 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+2224G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504204 | |||||||
| chr3:8504215 | G | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+2235G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504215 | |||||||
| chr3:8504255 | T | G | 1 | a0001c0001t0002g0136 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.42+2275T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504255 | |||||||
| chr3:8504325 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.42+2345G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504325 | |||||||
| chr3:8504416 | G | A | 82 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0249 others(79): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.42+2436G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504416 | |||||||
| chr3:8504468 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42+2488C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504468 | |||||||
| chr3:8504595 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.42+2615G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504595 | |||||||
| chr3:8504625 | C | T | 3 | a0001c0001t0001g0231 a0001c0001t0003g0232 a0001c0001t0003g0233 |
3 | HG02155.hp1 NA18943.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.42+2645C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504625 | |||||||
| chr3:8504639 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.42+2659C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504639 | |||||||
| chr3:8504663 | A | C | 1 | a0001c0001t0003g0293 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.42+2683A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504663 | |||||||
| chr3:8504897 | G | A | 2 | a0001c0001t0003g0246 a0001c0001t0035g0247 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.42+2917G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504897 | |||||||
| chr3:8504929 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.42+2949C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504929 | |||||||
| chr3:8504935 | C | G | 1 | a0001c0002t0004g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42+2955C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504935 | |||||||
| chr3:8505276 | A | C | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+3296A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505276 | |||||||
| chr3:8505306 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(100): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.42+3326G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505306 | |||||||
| chr3:8505401 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.42+3421G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505401 | |||||||
| chr3:8505677 | G | C | 1 | a0001c0001t0012g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.42+3697G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505677 | |||||||
| chr3:8505706 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.42+3726T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505706 | |||||||
| chr3:8505733 | C | A | 3 | a0001c0001t0002g0135 a0001c0002t0002g0190 a0001c0002t0004g0078 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+3753C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505733 | |||||||
| chr3:8505764 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01081.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+3784T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505764 | |||||||
| chr3:8505765 | T | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0299 a0001c0001t0002g0030 others(24): Show |
27 | HG00423.hp1 HG01169.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+3785T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505765 | |||||||
| chr3:8505917 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.42+3937T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505917 | |||||||
| chr3:8506055 | C | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.42+4075C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506055 | |||||||
| chr3:8506138 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.42+4158C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506138 | |||||||
| chr3:8506177 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(100): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.42+4197T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506177 | |||||||
| chr3:8506187 | G | A | 3 | a0001c0001t0002g0227 a0001c0002t0002g0191 a0001c0002t0004g0225 |
3 | HG01081.hp1 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.42+4207G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506187 | |||||||
| chr3:8506296 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.42+4316T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506296 | |||||||
| chr3:8506362 | T | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.42+4382T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506362 | |||||||
| chr3:8506369 | C | A | 1 | a0001c0001t0003g0138 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.42+4389C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506369 | |||||||
| chr3:8506546 | A | T | 15 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0003g0075 others(12): Show |
15 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+4566A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506546 | |||||||
| chr3:8506843 | G | A | 9 | a0001c0001t0031g0082 a0001c0002t0001g0197 a0001c0002t0001g0244 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+4863G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506843 | |||||||
| chr3:8506914 | G | A | 15 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0003g0075 others(12): Show |
15 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+4934G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506914 | |||||||
| chr3:8507141 | G | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(91): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.42+5161G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507141 | |||||||
| chr3:8507145 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+5165A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507145 | |||||||
| chr3:8507164 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(91): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.42+5184G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507164 | |||||||
| chr3:8507199 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.42+5219T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507199 | |||||||
| chr3:8507233 | G | A | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+5253G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507233 | |||||||
| chr3:8507512 | C | G | 2 | a0001c0001t0032g0134 a0001c0001t0033g0133 |
2 | HG00408.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.42+5532C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507512 | |||||||
| chr3:8507645 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.42+5665T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507645 | |||||||
| chr3:8507736 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.42+5756C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507736 | |||||||
| chr3:8507782 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.42+5802G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507782 | |||||||
| chr3:8507798 | A | T | 2 | a0001c0001t0004g0226 a0001c0001t0005g0192 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.42+5818A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507798 | |||||||
| chr3:8507904 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0002g0009 a0001c0001t0002g0061 others(18): Show |
23 | HG00438.hp1 HG00609.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.42+5924A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507904 | |||||||
| chr3:8507979 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.42+5999C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507979 | |||||||
| chr3:8507982 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42+6002G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507982 | |||||||
| chr3:8508223 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0003g0187 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+6243G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508223 | |||||||
| chr3:8508264 | A | G | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+6284A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508264 | |||||||
| chr3:8508275 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+6295C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508275 | |||||||
| chr3:8508329 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.42+6349C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508329 | |||||||
| chr3:8508677 | C | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.42+6697C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508677 | |||||||
| chr3:8508717 | C | G | 3 | a0001c0001t0002g0135 a0001c0002t0002g0190 a0001c0002t0004g0078 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+6737C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508717 | |||||||
| chr3:8508923 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.42+6943C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508923 | |||||||
| chr3:8509094 | A | G | 1 | a0001c0001t0002g0012 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.42+7114A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509094 | |||||||
| chr3:8509159 | G | A | 2 | a0001c0001t0021g0083 a0001c0001t0034g0238 |
2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.42+7179G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509159 | |||||||
| chr3:8509189 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42+7209G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509189 | |||||||
| chr3:8509216 | T | G | 1 | a0001c0001t0003g0140 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.42+7236T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509216 | |||||||
| chr3:8509426 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(224): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.42+7446A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509426 | |||||||
| chr3:8509471 | C | T | 24 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0135 others(21): Show |
24 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.42+7491C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509471 | |||||||
| chr3:8509648 | G | A | 1 | a0001c0001t0021g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.42+7668G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509648 | |||||||
| chr3:8509681 | A | C | 2 | a0001c0001t0021g0083 a0001c0001t0034g0238 |
2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.42+7701A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509681 | |||||||
| chr3:8509851 | C | T | 1 | a0001c0001t0036g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.42+7871C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509851 | |||||||
| chr3:8509963 | A | G | 24 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0135 others(21): Show |
24 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.42+7983A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509963 | |||||||
| chr3:8510059 | T | C | 22 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0135 others(19): Show |
22 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.42+8079T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510059 | |||||||
| chr3:8510164 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.42+8184C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510164 | |||||||
| chr3:8510193 | C | T | 6 | a0001c0001t0001g0286 a0001c0001t0003g0283 a0001c0001t0049g0285 others(3): Show |
8 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+8213C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510193 | |||||||
| chr3:8510349 | A | G | 1 | a0001c0001t0003g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.42+8369A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510349 | |||||||
| chr3:8510352 | G | C | 23 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0135 others(20): Show |
23 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.42+8372G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510352 | |||||||
| chr3:8510539 | T | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.42+8559T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510539 | |||||||
| chr3:8510571 | C | T | 1 | a0001c0002t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.42+8591C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510571 | |||||||
| chr3:8510754 | A | G | 1 | a0001c0001t0046g0204 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.42+8774A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510754 | |||||||
| chr3:8510866 | A | G | 1 | a0001c0001t0006g0113 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.42+8886A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510866 | |||||||
| chr3:8510953 | C | T | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+8973C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510953 | |||||||
| chr3:8511076 | C | T | 2 | a0001c0001t0004g0226 a0001c0001t0005g0192 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.42+9096C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511076 | |||||||
| chr3:8511401 | T | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(87): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.42+9421T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511401 | |||||||
| chr3:8511455 | T | C | 6 | a0001c0002t0001g0197 a0001c0002t0005g0196 a0001c0002t0008g0185 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+9475T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511455 | |||||||
| chr3:8511552 | G | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(87): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.42+9572G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511552 | |||||||
| chr3:8511681 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+9701A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511681 | |||||||
| chr3:8511932 | T | C | 1 | a0001c0002t0001g0244 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.42+9952T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511932 | |||||||
| chr3:8511977 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+9997T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511977 | |||||||
| chr3:8512305 | C | G | 14 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0003g0075 others(11): Show |
14 | HG00423.hp1 HG02258.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.42+10325C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512305 | |||||||
| chr3:8512345 | C | T | 3 | a0001c0001t0002g0135 a0001c0002t0002g0190 a0001c0002t0004g0078 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+10365C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512345 | |||||||
| chr3:8512366 | A | G | 12 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0003g0075 others(9): Show |
12 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+10386A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512366 | |||||||
| chr3:8512600 | G | A | 17 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0135 others(14): Show |
17 | HG00423.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.42+10620G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512600 | |||||||
| chr3:8512617 | C | T | 63 | a0001c0001t0001g0025 a0001c0001t0001g0249 a0001c0001t0001g0250 others(60): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.42+10637C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512617 | |||||||
| chr3:8512840 | A | G | 1 | a0005c0007t0025g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.42+10860A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512840 | |||||||
| chr3:8512948 | T | C | 11 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0003g0075 others(8): Show |
11 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+10968T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512948 | |||||||
| chr3:8513024 | A | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(289): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.42+11044A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8513024 | |||||||
| chr3:8513603 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.42+11623T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8513603 | |||||||
| chr3:8513821 | A | C | 64 | a0001c0001t0001g0025 a0001c0001t0001g0249 a0001c0001t0001g0250 others(61): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.42+11841A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8513821 | |||||||
| chr3:8514104 | G | GATAC | 4 | a0001c0001t0002g0181 a0001c0001t0015g0076 a0001c0001t0015g0077 others(1): Show |
4 | HG00673.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+12144_42+12147d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8514104 | ||||||
| chr3:8514211 | C | T | 3 | a0001c0001t0002g0135 a0001c0002t0002g0190 a0001c0002t0004g0078 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+12231C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514211 | |||||||
| chr3:8514302 | C | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+12322C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514302 | |||||||
| chr3:8514391 | A | G | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+12411A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514391 | |||||||
| chr3:8514511 | G | A | 1 | a0001c0001t0042g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.42+12531G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514511 | |||||||
| chr3:8514567 | T | G | 1 | a0001c0001t0004g0089 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.42+12587T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514567 | |||||||
| chr3:8514625 | G | A | 1 | a0001c0001t0021g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.42+12645G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514625 | |||||||
| chr3:8514694 | A | T | 2 | a0001c0001t0004g0226 a0001c0001t0005g0192 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.42+12714A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514694 | |||||||
| chr3:8514754 | G | A | 6 | a0001c0002t0001g0197 a0001c0002t0005g0196 a0001c0002t0008g0185 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+12774G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514754 | |||||||
| chr3:8514764 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.42+12784C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514764 | |||||||
| chr3:8514931 | A | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+12951A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514931 | |||||||
| chr3:8514963 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+12983C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514963 | |||||||
| chr3:8514985 | T | G | 47 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0299 others(44): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.42+13005T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514985 | |||||||
| chr3:8514987 | C | T | 1 | a0001c0001t0003g0233 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+13007C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514987 | |||||||
| chr3:8515067 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.42+13087G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515067 | |||||||
| chr3:8515098 | A | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.42+13118A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515098 | |||||||
| chr3:8515146 | G | A | 14 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0002g0135 others(11): Show |
14 | HG00423.hp1 HG02280.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.42+13166G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515146 | |||||||
| chr3:8515199 | T | C | 3 | a0001c0001t0002g0135 a0001c0002t0002g0190 a0001c0002t0004g0078 |
3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+13219T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515199 | |||||||
| chr3:8515223 | T | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(88): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.42+13243T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515223 | |||||||
| chr3:8515431 | C | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(78): Show |
86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.42+13451C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515431 | |||||||
| chr3:8515547 | A | G | 3 | a0001c0001t0001g0189 a0001c0001t0004g0226 a0001c0002t0004g0078 |
3 | HG02109.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.42+13567A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515547 | |||||||
| chr3:8515873 | T | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(88): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.42+13893T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515873 | |||||||
| chr3:8516002 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(99): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.42+14022C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516002 | |||||||
| chr3:8516160 | A | G | 65 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0086 others(62): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.42+14180A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516160 | |||||||
| chr3:8516189 | T | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.42+14209T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516189 | |||||||
| chr3:8516306 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
42 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.42+14326A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516306 | |||||||
| chr3:8516310 | G | A | 55 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(52): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.42+14330G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516310 | |||||||
| chr3:8516400 | A | G | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+14420A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516400 | |||||||
| chr3:8516428 | C | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14448C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516428 | |||||||
| chr3:8516429 | TG | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0045 |
3 | HG01256.hp1 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.42+14451delG | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8516429 | ||||||
| chr3:8516508 | T | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14528T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516508 | |||||||
| chr3:8516527 | C | T | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14547C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516527 | |||||||
| chr3:8516614 | G | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14634G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516614 | |||||||
| chr3:8516699 | A | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14719A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516699 | |||||||
| chr3:8516829 | T | C | 55 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(52): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.42+14849T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516829 | |||||||
| chr3:8516918 | T | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14938T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516918 | |||||||
| chr3:8516968 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42+14988G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516968 | |||||||
| chr3:8517054 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.42+15074C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517054 | |||||||
| chr3:8517137 | G | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+15157G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517137 | |||||||
| chr3:8517150 | G | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+15170G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517150 | |||||||
| chr3:8517155 | A | T | 3 | a0001c0001t0003g0280 a0001c0001t0003g0287 a0001c0001t0047g0276 |
3 | HG00642.hp2 HG01346.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.42+15175A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517155 | |||||||
| chr3:8517368 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43-15369T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517368 | |||||||
| chr3:8517370 | G | A | 3 | a0001c0001t0001g0255 a0001c0002t0002g0191 a0004c0011t0001g0254 |
3 | HG01081.hp1 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.43-15367G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517370 | |||||||
| chr3:8517477 | C | T | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-15260C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517477 | |||||||
| chr3:8517528 | T | C | 2 | a0001c0001t0002g0221 a0001c0001t0003g0214 |
2 | HG02056.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.43-15209T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517528 | |||||||
| chr3:8517604 | C | T | 4 | a0001c0001t0001g0286 a0001c0001t0049g0285 a0001c0002t0001g0002 others(1): Show |
6 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-15133C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517604 | |||||||
| chr3:8517833 | T | G | 1 | a0001c0001t0038g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43-14904T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517833 | |||||||
| chr3:8517959 | T | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14778T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517959 | |||||||
| chr3:8518052 | GA | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14674delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8518052 | ||||||
| chr3:8518132 | G | T | 1 | a0001c0001t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.43-14605G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518132 | |||||||
| chr3:8518167 | C | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14570C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518167 | |||||||
| chr3:8518170 | A | G | 55 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(52): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.43-14567A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518170 | |||||||
| chr3:8518368 | G | A | 74 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-14369G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518368 | |||||||
| chr3:8518452 | T | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14285T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518452 | |||||||
| chr3:8518482 | C | T | 1 | a0006c0006t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43-14255C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518482 | |||||||
| chr3:8518610 | A | G | 7 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(4): Show |
7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-14127A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518610 | |||||||
| chr3:8518637 | C | T | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-14100C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518637 | |||||||
| chr3:8518724 | A | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14013A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518724 | |||||||
| chr3:8518761 | A | C | 13 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0004g0031 others(10): Show |
14 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-13976A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518761 | |||||||
| chr3:8518783 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-13954G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518783 | |||||||
| chr3:8519007 | A | T | 1 | a0001c0002t0001g0032 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.43-13730A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519007 | |||||||
| chr3:8519096 | G | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
27 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.43-13641G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519096 | |||||||
| chr3:8519125 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.43-13612C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519125 | |||||||
| chr3:8519195 | A | G | 12 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0234 others(9): Show |
12 | HG00735.hp2 HG02074.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-13542A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519195 | |||||||
| chr3:8519371 | A | T | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.43-13366A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519371 | |||||||
| chr3:8519409 | T | C | 1 | a0001c0001t0010g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.43-13328T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519409 | |||||||
| chr3:8519454 | C | T | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-13283C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519454 | |||||||
| chr3:8519585 | C | T | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-13152C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519585 | |||||||
| chr3:8519740 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.43-12997G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519740 | |||||||
| chr3:8519741 | C | CA | 8 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0169 others(5): Show |
8 | HG00639.hp2 HG02615.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-12983dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519741 | ||||||
| chr3:8519741 | CA | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
25 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.43-12983delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519741 | ||||||
| chr3:8519750 | A | G | 2 | a0001c0001t0003g0167 a0001c0001t0003g0168 |
2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.43-12987A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519750 | |||||||
| chr3:8519753 | AAG | A | 12 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(9): Show |
12 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-12982_43-12981d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519753 | ||||||
| chr3:8519852 | TTTACCAT others(6): Show |
T | 1 | a0001c0002t0003g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.43-12883_43-12871d others(15): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519852 | ||||||
| chr3:8519907 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0189 a0001c0001t0003g0187 a0001c0001t0014g0188 |
3 | HG02647.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.43-12826_43-12819d others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519907 | ||||||
| chr3:8519917 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0206 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.43-12819_43-12818i others(12): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519917 | ||||||
| chr3:8519917 | T | TGTGTGTG others(5): Show |
2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-12819_43-12818i others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519917 | ||||||
| chr3:8519917 | T | TGTGTGTG others(7): Show |
7 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(4): Show |
7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-12819_43-12818i others(16): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519917 | ||||||
| chr3:8519925 | A | AGT | 14 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0004g0031 others(11): Show |
15 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-12793_43-12792d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519925 | ||||||
| chr3:8519925 | A | AGTGT | 5 | a0001c0001t0001g0294 a0001c0001t0002g0251 a0001c0001t0002g0252 others(2): Show |
5 | HG02572.hp1 HG03139.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-12795_43-12792d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519925 | ||||||
| chr3:8519925 | A | T | 7 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(4): Show |
7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-12812A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519925 | |||||||
| chr3:8519927 | T | A | 7 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-12810T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519927 | |||||||
| chr3:8519929 | T | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-12808T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519929 | |||||||
| chr3:8519966 | T | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-12771T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519966 | |||||||
| chr3:8520046 | T | C | 59 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0059 others(56): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.43-12691T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520046 | |||||||
| chr3:8520260 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-12477A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520260 | |||||||
| chr3:8520324 | T | C | 15 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(12): Show |
15 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-12413T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520324 | |||||||
| chr3:8520360 | A | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-12377A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520360 | |||||||
| chr3:8520606 | G | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-12131G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520606 | |||||||
| chr3:8520837 | T | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-11900T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520837 | |||||||
| chr3:8520951 | A | G | 62 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(59): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.43-11786A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520951 | |||||||
| chr3:8521058 | G | A | 2 | a0001c0001t0003g0241 a0001c0001t0044g0242 |
2 | HG00597.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.43-11679G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521058 | |||||||
| chr3:8521081 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43-11656C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521081 | |||||||
| chr3:8521370 | T | G | 1 | a0001c0002t0019g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43-11367T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521370 | |||||||
| chr3:8521458 | C | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
24 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-11279C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521458 | |||||||
| chr3:8521462 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-11275C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521462 | |||||||
| chr3:8521514 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0079 a0001c0002t0001g0253 |
4 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-11223G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521514 | |||||||
| chr3:8521558 | C | A | 2 | a0001c0002t0001g0085 a0001c0002t0003g0222 |
2 | HG02735.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.43-11179C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521558 | |||||||
| chr3:8521582 | T | C | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.43-11155T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521582 | |||||||
| chr3:8521715 | T | A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-11022T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521715 | |||||||
| chr3:8521743 | T | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-10994T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521743 | |||||||
| chr3:8521755 | C | A | 1 | a0001c0002t0002g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-10982C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521755 | |||||||
| chr3:8521769 | A | C | 57 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(54): Show |
60 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.43-10968A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521769 | |||||||
| chr3:8521791 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(100): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.43-10946G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521791 | |||||||
| chr3:8521825 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.43-10912G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521825 | |||||||
| chr3:8521891 | G | T | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-10846G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521891 | |||||||
| chr3:8521898 | GT | G | 4 | a0001c0001t0001g0086 a0001c0001t0004g0226 a0001c0001t0021g0083 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-10831delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8521898 | ||||||
| chr3:8521977 | A | G | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10760A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521977 | |||||||
| chr3:8521987 | A | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(11): Show |
14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-10750A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521987 | |||||||
| chr3:8522071 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.43-10666G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522071 | |||||||
| chr3:8522396 | C | G | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10341C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522396 | |||||||
| chr3:8522439 | G | A | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10298G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522439 | |||||||
| chr3:8522749 | G | A | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.43-9988G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522749 | |||||||
| chr3:8522809 | TTTAAAAA | T | 6 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0005g0196 others(3): Show |
6 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-9915_43-9909del others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8522809 | ||||||
| chr3:8522964 | C | T | 13 | a0001c0001t0001g0299 a0001c0001t0002g0030 a0001c0001t0004g0031 others(10): Show |
14 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-9773C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522964 | |||||||
| chr3:8523011 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.43-9726A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523011 | |||||||
| chr3:8523253 | T | C | 59 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(56): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.43-9484T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523253 | |||||||
| chr3:8523577 | A | G | 59 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(56): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.43-9160A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523577 | |||||||
| chr3:8523835 | A | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
25 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.43-8902A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523835 | |||||||
| chr3:8524018 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.43-8719A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524018 | |||||||
| chr3:8524074 | T | G | 1 | a0001c0001t0002g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8663T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524074 | |||||||
| chr3:8524200 | G | GA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0235 a0001c0001t0001g0249 others(5): Show |
8 | HG02055.hp1 HG02055.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-8517dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8524200 | ||||||
| chr3:8524201 | A | G | 1 | a0001c0001t0007g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-8536A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524201 | |||||||
| chr3:8524465 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-8272A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524465 | |||||||
| chr3:8524602 | A | G | 1 | a0001c0001t0012g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.43-8135A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524602 | |||||||
| chr3:8524681 | A | G | 73 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(70): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.43-8056A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524681 | |||||||
| chr3:8524687 | C | CTGTTGT | 73 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(70): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.43-8038_43-8033dup others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8524687 | ||||||
| chr3:8524925 | G | T | 73 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(70): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.43-7812G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524925 | |||||||
| chr3:8524969 | G | A | 12 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(9): Show |
12 | HG01081.hp1 HG01169.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-7768G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524969 | |||||||
| chr3:8525075 | A | T | 73 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(70): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.43-7662A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525075 | |||||||
| chr3:8525159 | T | C | 73 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(70): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.43-7578T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525159 | |||||||
| chr3:8525165 | C | G | 1 | a0005c0007t0025g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43-7572C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525165 | |||||||
| chr3:8525569 | T | G | 76 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(73): Show |
79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-7168T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525569 | |||||||
| chr3:8525754 | C | T | 1 | a0001c0001t0003g0010 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.43-6983C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525754 | |||||||
| chr3:8525874 | T | G | 75 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-6863T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525874 | |||||||
| chr3:8526189 | A | G | 1 | a0001c0001t0003g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43-6548A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526189 | |||||||
| chr3:8526250 | G | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-6487G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526250 | |||||||
| chr3:8526257 | G | A | 1 | a0001c0001t0003g0246 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.43-6480G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526257 | |||||||
| chr3:8526495 | CAGTT | C | 74 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-6236_43-6233del others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8526495 | ||||||
| chr3:8526640 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-6097T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526640 | |||||||
| chr3:8526782 | A | G | 75 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-5955A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526782 | |||||||
| chr3:8526940 | G | A | 8 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(5): Show |
11 | HG00099.hp2 HG00642.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-5797G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526940 | |||||||
| chr3:8527236 | C | A | 8 | a0001c0001t0001g0093 a0001c0001t0001g0224 a0001c0001t0001g0235 others(5): Show |
8 | HG00544.hp2 HG02165.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-5501C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527236 | |||||||
| chr3:8527270 | T | C | 74 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-5467T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527270 | |||||||
| chr3:8527284 | C | G | 7 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(4): Show |
7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-5453C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527284 | |||||||
| chr3:8527291 | T | C | 74 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-5446T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527291 | |||||||
| chr3:8527376 | G | C | 5 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-5361G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527376 | |||||||
| chr3:8527436 | G | T | 2 | a0001c0001t0002g0181 a0001c0001t0016g0180 |
2 | HG00673.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.43-5301G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527436 | |||||||
| chr3:8527446 | G | A | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-5291G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527446 | |||||||
| chr3:8527508 | A | G | 74 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0186 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-5229A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527508 | |||||||
| chr3:8527523 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(101): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.43-5214T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527523 | |||||||
| chr3:8527649 | T | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0044 others(1): Show |
4 | HG01255.hp2 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-5088T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527649 | |||||||
| chr3:8527675 | C | T | 3 | a0001c0002t0002g0190 a0001c0002t0002g0236 a0001c0002t0002g0237 |
3 | HG02280.hp2 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-5062C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527675 | |||||||
| chr3:8527711 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-5026C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527711 | |||||||
| chr3:8527798 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(293): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.43-4939T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527798 | |||||||
| chr3:8527888 | G | C | 1 | a0002c0003t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43-4849G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527888 | |||||||
| chr3:8527905 | T | C | 1 | a0001c0001t0009g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43-4832T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527905 | |||||||
| chr3:8527939 | A | G | 14 | a0001c0001t0001g0299 a0001c0001t0026g0064 a0001c0001t0027g0092 others(11): Show |
15 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-4798A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527939 | |||||||
| chr3:8528107 | G | A | 20 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(17): Show |
20 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.43-4630G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528107 | |||||||
| chr3:8528315 | A | G | 1 | a0002c0003t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43-4422A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528315 | |||||||
| chr3:8528352 | G | GT | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
33 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.43-4376dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8528352 | ||||||
| chr3:8528352 | GT | G | 74 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(71): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-4376delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8528352 | ||||||
| chr3:8528359 | T | G | 2 | a0001c0001t0010g0046 a0001c0001t0010g0091 |
2 | NA18965.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.43-4378T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528359 | |||||||
| chr3:8528374 | C | T | 74 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(71): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-4363C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528374 | |||||||
| chr3:8528386 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-4351G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528386 | |||||||
| chr3:8528704 | G | A | 74 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(71): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-4033G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528704 | |||||||
| chr3:8528740 | C | T | 74 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(71): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-3997C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528740 | |||||||
| chr3:8528760 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-3977C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528760 | |||||||
| chr3:8528856 | G | C | 1 | a0001c0001t0031g0082 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43-3881G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528856 | |||||||
| chr3:8528991 | G | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-3746G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528991 | |||||||
| chr3:8529188 | A | G | 74 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(71): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-3549A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529188 | |||||||
| chr3:8529309 | G | A | 2 | a0001c0001t0014g0296 a0001c0001t0052g0295 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.43-3428G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529309 | |||||||
| chr3:8529424 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(52): Show |
59 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.43-3313G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529424 | |||||||
| chr3:8529451 | G | A | 1 | a0001c0001t0003g0065 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.43-3286G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529451 | |||||||
| chr3:8529471 | G | GA | 89 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(86): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.43-3266_43-3265ins others(1): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529471 | |||||||
| chr3:8529499 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-3238C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529499 | |||||||
| chr3:8529532 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-3205C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529532 | |||||||
| chr3:8529535 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.43-3202C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529535 | |||||||
| chr3:8529548 | G | A | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-3189G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529548 | |||||||
| chr3:8529802 | C | A | 1 | a0001c0002t0004g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.43-2935C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529802 | |||||||
| chr3:8529965 | C | T | 6 | a0001c0002t0001g0244 a0001c0002t0002g0190 a0001c0002t0005g0196 others(3): Show |
6 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-2772C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529965 | |||||||
| chr3:8530124 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.43-2613A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530124 | |||||||
| chr3:8530246 | G | C | 1 | a0001c0001t0003g0293 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.43-2491G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530246 | |||||||
| chr3:8530402 | C | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.43-2335C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530402 | |||||||
| chr3:8530687 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(94): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.43-2050G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530687 | |||||||
| chr3:8531086 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43-1651G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531086 | |||||||
| chr3:8531150 | A | G | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1587A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531150 | |||||||
| chr3:8531343 | C | T | 16 | a0001c0001t0001g0299 a0001c0001t0026g0064 a0001c0001t0027g0092 others(13): Show |
16 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-1394C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531343 | |||||||
| chr3:8531409 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(250): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.43-1328T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531409 | |||||||
| chr3:8531482 | C | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0168 |
2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.43-1255C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531482 | |||||||
| chr3:8531578 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.43-1159T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531578 | |||||||
| chr3:8531957 | T | G | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-780T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531957 | |||||||
| chr3:8532296 | G | A | 1 | a0001c0001t0018g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.43-441G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532296 | |||||||
| chr3:8532320 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.43-417C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532320 | |||||||
| chr3:8532360 | C | G | 1 | a0001c0001t0003g0162 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.43-377C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532360 | |||||||
| chr3:8532406 | G | A | 3 | a0001c0001t0010g0046 a0001c0001t0010g0091 a0006c0006t0001g0228 |
3 | NA18522.hp1 NA18965.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.43-331G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532406 | |||||||
| chr3:8532444 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.43-293G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532444 | |||||||
| chr3:8532549 | C | G | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-188C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532549 | |||||||
| chr3:8532686 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.43-51C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532686 | |||||||
| chr3:8532927 | G | C | 5 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.131+102G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8532927 | |||||||
| chr3:8533166 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.131+341G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533166 | |||||||
| chr3:8533397 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+572A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533397 | |||||||
| chr3:8533436 | T | A | 1 | a0001c0001t0003g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.131+611T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533436 | |||||||
| chr3:8533560 | G | A | 2 | a0001c0001t0026g0064 a0001c0001t0027g0092 |
2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.131+735G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533560 | |||||||
| chr3:8533725 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
44 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.131+900C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533725 | |||||||
| chr3:8533812 | A | G | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+987A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533812 | |||||||
| chr3:8533821 | T | A | 1 | a0001c0008t0002g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.131+996T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533821 | |||||||
| chr3:8533867 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(65): Show |
71 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+1042A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533867 | |||||||
| chr3:8533918 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131+1093G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533918 | |||||||
| chr3:8534159 | G | A | 20 | a0001c0001t0001g0299 a0001c0002t0001g0002 a0001c0002t0001g0006 others(17): Show |
23 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.131+1334G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534159 | |||||||
| chr3:8534208 | C | G | 1 | a0001c0001t0002g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.131+1383C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534208 | |||||||
| chr3:8534369 | C | A | 1 | a0001c0001t0004g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.131+1544C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534369 | |||||||
| chr3:8534715 | T | C | 27 | a0001c0001t0001g0299 a0001c0002t0001g0002 a0001c0002t0001g0006 others(24): Show |
30 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.131+1890T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534715 | |||||||
| chr3:8534754 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.131+1929G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534754 | |||||||
| chr3:8534754 | G | T | 1 | a0001c0001t0048g0096 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.131+1929G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534754 | |||||||
| chr3:8535323 | A | AT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.132-1854dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 8535323 | ||||||
| chr3:8535374 | G | A | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.132-1811G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535374 | |||||||
| chr3:8535551 | G | A | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.132-1634G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535551 | |||||||
| chr3:8535616 | A | G | 3 | a0001c0001t0003g0044 a0001c0001t0003g0283 a0001c0001t0049g0285 |
3 | HG01192.hp2 HG01255.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.132-1569A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535616 | |||||||
| chr3:8535662 | A | C | 1 | a0001c0001t0051g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.132-1523A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535662 | |||||||
| chr3:8536128 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.132-1057C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536128 | |||||||
| chr3:8536157 | G | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.132-1028G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536157 | |||||||
| chr3:8536286 | G | A | 7 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(4): Show |
7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-899G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536286 | |||||||
| chr3:8536293 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.132-892G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536293 | |||||||
| chr3:8536399 | G | A | 1 | a0001c0001t0006g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.132-786G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536399 | |||||||
| chr3:8536505 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.132-680C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536505 | |||||||
| chr3:8536566 | C | T | 1 | a0001c0001t0003g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.132-619C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536566 | |||||||
| chr3:8536582 | A | G | 6 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0003g0070 others(3): Show |
6 | NA18747.hp1 NA18970.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-603A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536582 | |||||||
| chr3:8536608 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0003g0284 |
4 | HG00642.hp1 HG00741.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.132-577C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536608 | |||||||
| chr3:8536798 | G | T | 1 | a0001c0008t0002g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.132-387G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536798 | |||||||
| chr3:8536911 | G | A | 36 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0001t0013g0297 others(33): Show |
39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.132-274G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536911 | |||||||
| chr3:8536975 | C | G | 1 | a0001c0001t0003g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132-210C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536975 | |||||||
| chr3:8537062 | C | T | 36 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0001t0013g0297 others(33): Show |
39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.132-123C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8537062 | |||||||
| chr3:8537450 | C | T | 1 | a0001c0001t0003g0218 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.387+10C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537450 | |||||||
| chr3:8537604 | G | A | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+164G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537604 | |||||||
| chr3:8537656 | G | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0023 others(45): Show |
51 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.387+216G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537656 | |||||||
| chr3:8537996 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
8 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.387+556G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537996 | |||||||
| chr3:8538044 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.387+604G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538044 | |||||||
| chr3:8538164 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(58): Show |
64 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.387+724G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538164 | |||||||
| chr3:8538166 | G | C | 1 | a0001c0001t0004g0016 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.387+726G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538166 | |||||||
| chr3:8538266 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(92): Show |
101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.387+826C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538266 | |||||||
| chr3:8538286 | G | A | 1 | a0001c0002t0004g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.387+846G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538286 | |||||||
| chr3:8538351 | A | G | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+911A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538351 | |||||||
| chr3:8538375 | T | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(92): Show |
101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.387+935T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538375 | |||||||
| chr3:8538405 | T | C | 28 | a0001c0001t0001g0299 a0001c0002t0001g0002 a0001c0002t0001g0006 others(25): Show |
31 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.387+965T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538405 | |||||||
| chr3:8538531 | C | T | 2 | a0001c0001t0017g0229 a0001c0001t0017g0230 |
2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.387+1091C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538531 | |||||||
| chr3:8538551 | C | G | 52 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(49): Show |
54 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.387+1111C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538551 | |||||||
| chr3:8538614 | C | T | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+1174C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538614 | |||||||
| chr3:8538707 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.387+1267T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538707 | |||||||
| chr3:8538795 | AC | A | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+1358delC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8538795 | ||||||
| chr3:8538800 | G | T | 34 | a0001c0001t0001g0299 a0001c0001t0002g0227 a0001c0002t0001g0002 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+1360G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538800 | |||||||
| chr3:8539093 | G | A | 1 | a0001c0008t0002g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.387+1653G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539093 | |||||||
| chr3:8539246 | GAA | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0044 others(3): Show |
6 | HG01192.hp2 HG01255.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1809_387+1810d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539246 | ||||||
| chr3:8539459 | C | A | 7 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(4): Show |
7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+2019C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539459 | |||||||
| chr3:8539477 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.387+2037G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539477 | |||||||
| chr3:8539512 | G | T | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2072G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539512 | |||||||
| chr3:8539656 | G | A | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2216G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539656 | |||||||
| chr3:8539795 | T | TTTA | 59 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0033 others(56): Show |
61 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.387+2397_387+2399d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | ||||||
| chr3:8539795 | T | TTTATTA | 4 | a0001c0001t0001g0150 a0001c0001t0015g0076 a0001c0001t0018g0148 others(1): Show |
4 | HG00323.hp1 HG00609.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+2394_387+2399d others(8): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | ||||||
| chr3:8539795 | TTTA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(89): Show |
96 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.387+2397_387+2399d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | ||||||
| chr3:8539795 | TTTATTA | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0186 a0001c0001t0001g0189 others(6): Show |
9 | HG01255.hp2 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+2394_387+2399d others(8): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | ||||||
| chr3:8539795 | TTTATTAT others(2): Show |
T | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2391_387+2399d others(11): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | ||||||
| chr3:8539795 | TTTATTAT others(8): Show |
T | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387+2385_387+2399d others(17): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | ||||||
| chr3:8539910 | G | GTGTGCTG others(45): Show |
11 | a0001c0002t0001g0002 a0001c0002t0001g0085 a0001c0002t0003g0112 others(8): Show |
13 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.387+2470_387+2471i others(54): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539910 | |||||||
| chr3:8539911 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(76): Show |
83 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.387+2471C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539911 | |||||||
| chr3:8539911 | C | TGTGCTGC others(45): Show |
5 | a0001c0002t0001g0032 a0001c0002t0003g0028 a0001c0002t0004g0084 others(2): Show |
5 | HG03017.hp1 HG03669.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2470_387+2471i others(54): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539911 | |||||||
| chr3:8539934 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0003g0007 |
3 | NA18953.hp2 NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.387+2494A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539934 | |||||||
| chr3:8539971 | C | G | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2531C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539971 | |||||||
| chr3:8539972 | A | AG | 31 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0059 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.387+2534dupG | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539972 | ||||||
| chr3:8540043 | A | G | 2 | a0001c0001t0002g0170 a0001c0001t0028g0176 |
2 | NA18950.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.387+2603A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540043 | |||||||
| chr3:8540571 | A | T | 1 | a0001c0002t0011g0027 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.387+3131A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540571 | |||||||
| chr3:8540590 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.387+3150G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540590 | |||||||
| chr3:8540682 | G | A | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+3242G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540682 | |||||||
| chr3:8540737 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(103): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.387+3297G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540737 | |||||||
| chr3:8540786 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(50): Show |
55 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.387+3346G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540786 | |||||||
| chr3:8540816 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.387+3376C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540816 | |||||||
| chr3:8540977 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(92): Show |
101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.387+3537T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540977 | |||||||
| chr3:8541102 | C | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+3662C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541102 | |||||||
| chr3:8541144 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.387+3704T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541144 | |||||||
| chr3:8541298 | C | G | 1 | a0001c0002t0004g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.387+3858C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541298 | |||||||
| chr3:8541365 | C | A | 52 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(49): Show |
54 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.387+3925C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541365 | |||||||
| chr3:8541378 | C | G | 1 | a0001c0002t0004g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.387+3938C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541378 | |||||||
| chr3:8541473 | C | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+4033C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541473 | |||||||
| chr3:8541582 | A | G | 1 | a0001c0001t0006g0104 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.387+4142A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541582 | |||||||
| chr3:8541610 | C | T | 1 | a0001c0002t0005g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387+4170C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541610 | |||||||
| chr3:8541874 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.387+4434G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541874 | |||||||
| chr3:8542002 | C | CT | 42 | a0001c0001t0001g0059 a0001c0001t0001g0103 a0001c0001t0001g0275 others(39): Show |
45 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.387+4586dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8542002 | ||||||
| chr3:8542002 | C | CTT | 49 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0249 others(46): Show |
51 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.387+4585_387+4586d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8542002 | ||||||
| chr3:8542002 | C | CTTT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(15): Show |
19 | HG00735.hp1 HG01109.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.387+4584_387+4586d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8542002 | ||||||
| chr3:8542205 | T | C | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.387+4765T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542205 | |||||||
| chr3:8542551 | C | G | 1 | a0006c0006t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387+5111C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542551 | |||||||
| chr3:8542606 | C | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(91): Show |
100 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.387+5166C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542606 | |||||||
| chr3:8542835 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387+5395C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542835 | |||||||
| chr3:8542837 | T | G | 1 | a0001c0002t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.387+5397T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542837 | |||||||
| chr3:8542960 | G | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(92): Show |
101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.387+5520G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542960 | |||||||
| chr3:8543023 | G | T | 1 | a0001c0001t0002g0136 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.388-5545G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543023 | |||||||
| chr3:8543072 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.388-5496A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543072 | |||||||
| chr3:8543080 | A | G | 2 | a0001c0001t0003g0187 a0001c0001t0014g0188 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-5488A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543080 | |||||||
| chr3:8543180 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.388-5388G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543180 | |||||||
| chr3:8543313 | G | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.388-5255G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543313 | |||||||
| chr3:8543315 | G | A | 1 | a0001c0001t0006g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.388-5253G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543315 | |||||||
| chr3:8543377 | CTGATAGA others(12): Show |
C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(49): Show |
54 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.388-5170_388-5152d others(21): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543377 | ||||||
| chr3:8543378 | TGATAGAT others(16): Show |
T | 21 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0262 others(18): Show |
23 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-5170_388-5148d others(25): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | ||||||
| chr3:8543378 | TGATAGAT others(20): Show |
T | 2 | a0001c0001t0003g0246 a0001c0002t0001g0006 |
2 | HG01175.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.388-5170_388-5144d others(29): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | ||||||
| chr3:8543378 | TGATAGAT others(24): Show |
T | 1 | a0001c0001t0036g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.388-5170_388-5140d others(33): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | ||||||
| chr3:8543378 | TGATAGAT others(28): Show |
T | 3 | a0001c0002t0001g0085 a0001c0002t0001g0197 a0001c0002t0005g0196 |
3 | HG02818.hp1 HG03927.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.388-5170_388-5136d others(37): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | ||||||
| chr3:8543378 | TGATAGAT others(32): Show |
T | 4 | a0001c0002t0002g0190 a0001c0002t0008g0185 a0001c0002t0008g0194 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-5170_388-5132d others(41): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | ||||||
| chr3:8543382 | AGATAGAT others(8): Show |
A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0249 a0001c0001t0001g0250 others(5): Show |
8 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-5170_388-5156d others(17): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543382 | ||||||
| chr3:8543386 | AGATAGAT others(4): Show |
A | 4 | a0001c0001t0003g0241 a0001c0001t0012g0248 a0001c0001t0039g0268 others(1): Show |
4 | HG00323.hp1 HG01515.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-5170_388-5160d others(13): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543386 | ||||||
| chr3:8543397 | T | TAGATA | 3 | a0001c0001t0002g0273 a0001c0001t0003g0233 a0001c0001t0031g0082 |
3 | HG02717.hp1 NA18943.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.388-5171_388-5170i others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543397 | |||||||
| chr3:8543397 | T | TGATA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0045 others(30): Show |
34 | HG00673.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.388-5128_388-5125d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | ||||||
| chr3:8543397 | T | TGATAGAT others(1): Show |
22 | a0001c0001t0001g0041 a0001c0001t0001g0150 a0001c0001t0002g0053 others(19): Show |
22 | HG00140.hp2 HG01074.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.388-5132_388-5125d others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | ||||||
| chr3:8543397 | T | TGATAGAT others(5): Show |
7 | a0001c0001t0001g0102 a0001c0001t0001g0160 a0001c0001t0003g0282 others(4): Show |
7 | HG00408.hp1 HG01975.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-5136_388-5125d others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | ||||||
| chr3:8543397 | TGATA | T | 22 | a0001c0001t0001g0035 a0001c0001t0001g0151 a0001c0001t0001g0234 others(19): Show |
23 | HG00544.hp1 HG01192.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-5128_388-5125d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | ||||||
| chr3:8543397 | TGATAGAT others(1): Show |
T | 5 | a0001c0001t0001g0125 a0001c0001t0002g0177 a0001c0001t0003g0010 others(2): Show |
6 | HG00735.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-5132_388-5125d others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | ||||||
| chr3:8543424 | T | C | 1 | a0001c0001t0039g0268 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.388-5144T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543424 | |||||||
| chr3:8543440 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0002g0012 others(3): Show |
7 | HG00323.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-5128T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543440 | |||||||
| chr3:8543440 | T | TAGATAGA others(1): Show |
4 | a0001c0001t0001g0206 a0001c0001t0002g0038 a0001c0001t0003g0187 others(1): Show |
4 | HG01433.hp2 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-5125_388-5124i others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | ||||||
| chr3:8543440 | T | TAGATAGA others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0155 a0001c0001t0037g0001 |
3 | NA19057.hp1 NA19057.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.388-5125_388-5124i others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | ||||||
| chr3:8543440 | T | TAGATAGA others(9): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0007c0012t0001g0099 |
3 | HG02132.hp1 NA18612.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.388-5125_388-5124i others(18): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | ||||||
| chr3:8543440 | T | TAGATAGA others(17): Show |
1 | a0001c0001t0001g0186 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.388-5125_388-5124i others(26): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | ||||||
| chr3:8543444 | C | T | 32 | a0001c0001t0002g0126 a0001c0001t0002g0227 a0001c0001t0003g0271 others(29): Show |
35 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.388-5124C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543444 | |||||||
| chr3:8543492 | C | CAGAT | 4 | a0001c0001t0001g0123 a0001c0001t0002g0144 a0001c0001t0003g0048 others(1): Show |
4 | HG02300.hp1 HG02300.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-5063_388-5060d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543492 | ||||||
| chr3:8543518 | T | C | 2 | a0001c0001t0009g0115 a0001c0001t0010g0118 |
2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.388-5050T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543518 | |||||||
| chr3:8543551 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.388-5017C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543551 | |||||||
| chr3:8543639 | C | T | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-4929C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543639 | |||||||
| chr3:8543682 | T | C | 1 | a0003c0010t0002g0119 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.388-4886T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543682 | |||||||
| chr3:8543785 | G | A | 54 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(51): Show |
56 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.388-4783G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543785 | |||||||
| chr3:8544139 | TTC | T | 8 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(5): Show |
8 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-4419_388-4418d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8544139 | ||||||
| chr3:8544221 | A | G | 89 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.388-4347A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544221 | |||||||
| chr3:8544283 | T | C | 89 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.388-4285T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544283 | |||||||
| chr3:8544493 | G | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(85): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.388-4075G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544493 | |||||||
| chr3:8544673 | G | C | 1 | a0001c0002t0001g0244 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.388-3895G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544673 | |||||||
| chr3:8544755 | G | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(85): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.388-3813G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544755 | |||||||
| chr3:8544779 | C | A | 88 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(85): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.388-3789C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544779 | |||||||
| chr3:8544816 | A | G | 89 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(86): Show |
94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.388-3752A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544816 | |||||||
| chr3:8544851 | A | C | 1 | a0001c0001t0002g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388-3717A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544851 | |||||||
| chr3:8544954 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.388-3614G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544954 | |||||||
| chr3:8545025 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.388-3543C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545025 | |||||||
| chr3:8545105 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.388-3463G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545105 | |||||||
| chr3:8545246 | G | T | 1 | a0001c0001t0046g0204 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.388-3322G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545246 | |||||||
| chr3:8545416 | A | C | 1 | a0002c0003t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.388-3152A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545416 | |||||||
| chr3:8545488 | C | T | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-3080C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545488 | |||||||
| chr3:8545495 | T | C | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-3073T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545495 | |||||||
| chr3:8545578 | G | C | 1 | a0001c0001t0002g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388-2990G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545578 | |||||||
| chr3:8545622 | A | C | 1 | a0001c0001t0003g0168 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.388-2946A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545622 | |||||||
| chr3:8545721 | A | C | 1 | a0001c0001t0001g0235 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.388-2847A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545721 | |||||||
| chr3:8545864 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0139 |
2 | HG01192.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.388-2704G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545864 | |||||||
| chr3:8545930 | C | T | 4 | a0001c0001t0003g0106 a0001c0001t0006g0055 a0001c0001t0006g0104 others(1): Show |
4 | HG00673.hp1 NA18992.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-2638C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545930 | |||||||
| chr3:8545956 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0059 others(50): Show |
55 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.388-2612G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545956 | |||||||
| chr3:8545976 | A | C | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.388-2592A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545976 | |||||||
| chr3:8545984 | G | A | 19 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(16): Show |
22 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.388-2584G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545984 | |||||||
| chr3:8545999 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.388-2569C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545999 | |||||||
| chr3:8546004 | A | C | 1 | a0001c0001t0003g0007 | 2 | NA18953.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.388-2564A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546004 | |||||||
| chr3:8546071 | T | C | 1 | a0006c0006t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.388-2497T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546071 | |||||||
| chr3:8546119 | C | G | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.388-2449C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546119 | |||||||
| chr3:8546155 | A | C | 1 | a0001c0001t0046g0204 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.388-2413A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546155 | |||||||
| chr3:8546425 | A | G | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-2143A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546425 | |||||||
| chr3:8546487 | A | G | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-2081A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546487 | |||||||
| chr3:8546588 | T | C | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-1980T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546588 | |||||||
| chr3:8546663 | G | GT | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-1903dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8546663 | ||||||
| chr3:8546807 | G | A | 1 | a0001c0008t0002g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388-1761G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546807 | |||||||
| chr3:8546817 | C | T | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-1751C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546817 | |||||||
| chr3:8546818 | G | A | 1 | a0001c0001t0003g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.388-1750G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546818 | |||||||
| chr3:8547107 | C | T | 3 | a0001c0002t0001g0006 a0001c0002t0001g0079 a0001c0002t0001g0253 |
4 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1461C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547107 | |||||||
| chr3:8547113 | T | C | 1 | a0001c0002t0011g0027 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.388-1455T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547113 | |||||||
| chr3:8547163 | C | G | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-1405C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547163 | |||||||
| chr3:8547364 | C | T | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-1204C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547364 | |||||||
| chr3:8547380 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.388-1188T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547380 | |||||||
| chr3:8547401 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-1167G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547401 | |||||||
| chr3:8547510 | C | G | 1 | a0001c0001t0004g0291 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.388-1058C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547510 | |||||||
| chr3:8547688 | C | A | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-880C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547688 | |||||||
| chr3:8547696 | T | C | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-872T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547696 | |||||||
| chr3:8547699 | C | T | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-869C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547699 | |||||||
| chr3:8547736 | CA | C | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-825delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8547736 | ||||||
| chr3:8547746 | A | AGCCGGGC | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(284): Show |
298 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.388-820_388-819ins others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8547746 | ||||||
| chr3:8547849 | G | A | 1 | a0001c0002t0001g0244 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.388-719G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547849 | |||||||
| chr3:8547872 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
47 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.388-696C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547872 | |||||||
| chr3:8547885 | C | CA | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-673dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8547885 | ||||||
| chr3:8547894 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-674A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547894 | |||||||
| chr3:8547964 | T | C | 4 | a0001c0001t0003g0271 a0001c0001t0014g0296 a0001c0001t0052g0295 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-604T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547964 | |||||||
| chr3:8548167 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.388-401G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548167 | |||||||
| chr3:8548196 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.388-372G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548196 | |||||||
| chr3:8548220 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(93): Show |
102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.388-348T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548220 | |||||||
| chr3:8548263 | T | C | 1 | a0001c0001t0036g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.388-305T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548263 | |||||||
| chr3:8548271 | C | T | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.388-297C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548271 | |||||||
| chr3:8548329 | G | GT | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-233dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8548329 | ||||||
| chr3:8548925 | A | C | 1 | a0001c0001t0003g0157 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.723+22A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8548925 | |||||||
| chr3:8549120 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.723+217G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549120 | |||||||
| chr3:8549268 | G | A | 31 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(28): Show |
32 | HG00597.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.723+365G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549268 | |||||||
| chr3:8549298 | A | C | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.723+395A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549298 | |||||||
| chr3:8549489 | A | T | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.723+586A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549489 | |||||||
| chr3:8549664 | T | G | 32 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(29): Show |
35 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.723+761T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549664 | |||||||
| chr3:8549724 | G | T | 1 | a0001c0001t0005g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.723+821G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549724 | |||||||
| chr3:8549764 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.723+861T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549764 | |||||||
| chr3:8549783 | G | A | 19 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(16): Show |
22 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.723+880G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549783 | |||||||
| chr3:8549790 | C | G | 32 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(29): Show |
35 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.723+887C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549790 | |||||||
| chr3:8549882 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.723+979C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549882 | |||||||
| chr3:8549889 | G | A | 9 | a0001c0002t0001g0197 a0001c0002t0001g0244 a0001c0002t0002g0190 others(6): Show |
9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+986G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549889 | |||||||
| chr3:8549899 | C | T | 1 | a0001c0002t0050g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.723+996C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549899 | |||||||
| chr3:8550228 | T | C | 32 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(29): Show |
35 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.723+1325T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550228 | |||||||
| chr3:8550245 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0002g0012 a0001c0001t0031g0082 |
4 | HG02717.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+1342C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550245 | |||||||
| chr3:8550258 | T | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+1355T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550258 | |||||||
| chr3:8550289 | G | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+1386G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550289 | |||||||
| chr3:8550430 | C | T | 1 | a0006c0006t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.723+1527C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550430 | |||||||
| chr3:8550431 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(251): Show |
264 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.723+1528A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550431 | |||||||
| chr3:8550665 | T | C | 34 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(31): Show |
35 | HG00597.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.723+1762T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550665 | |||||||
| chr3:8550727 | CT | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
93 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.723+1828delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8550727 | ||||||
| chr3:8550731 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723+1828T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550731 | |||||||
| chr3:8550887 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
82 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.723+1984G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550887 | |||||||
| chr3:8551117 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
82 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.723+2214T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551117 | |||||||
| chr3:8551248 | T | C | 35 | a0001c0001t0001g0125 a0001c0002t0001g0002 a0001c0002t0001g0006 others(32): Show |
38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.723+2345T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551248 | |||||||
| chr3:8551352 | G | A | 34 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0032 others(31): Show |
37 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.723+2449G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551352 | |||||||
| chr3:8551359 | A | C | 1 | a0001c0001t0002g0062 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.723+2456A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551359 | |||||||
| chr3:8551575 | G | A | 4 | a0001c0001t0002g0179 a0001c0001t0002g0245 a0001c0001t0003g0207 others(1): Show |
4 | HG01243.hp1 HG01258.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+2672G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551575 | |||||||
| chr3:8551755 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.723+2852G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551755 | |||||||
| chr3:8551799 | C | T | 33 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0249 others(30): Show |
34 | HG00597.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.723+2896C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551799 | |||||||
| chr3:8552004 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.723+3101G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552004 | |||||||
| chr3:8552313 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
10 | HG02145.hp2 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+3410G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552313 | |||||||
| chr3:8552509 | C | T | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+3606C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552509 | |||||||
| chr3:8552524 | G | C | 2 | a0001c0001t0002g0062 a0001c0001t0002g0131 |
2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.723+3621G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552524 | |||||||
| chr3:8552563 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723+3660G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552563 | |||||||
| chr3:8552726 | T | C | 1 | a0001c0001t0003g0182 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.723+3823T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552726 | |||||||
| chr3:8552815 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+3912C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552815 | |||||||
| chr3:8552914 | G | A | 14 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0231 others(11): Show |
14 | HG00735.hp2 HG02074.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.723+4011G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552914 | |||||||
| chr3:8553105 | C | T | 1 | a0001c0002t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.723+4202C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553105 | |||||||
| chr3:8553125 | A | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4222A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553125 | |||||||
| chr3:8553163 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4260C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553163 | |||||||
| chr3:8553311 | C | T | 27 | a0001c0001t0002g0227 a0001c0001t0003g0075 a0001c0001t0031g0082 others(24): Show |
30 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.723+4408C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553311 | |||||||
| chr3:8553357 | T | C | 1 | a0001c0001t0039g0268 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.723+4454T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553357 | |||||||
| chr3:8553377 | A | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
81 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.723+4474A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553377 | |||||||
| chr3:8553404 | G | T | 1 | a0001c0002t0041g0256 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.723+4501G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553404 | |||||||
| chr3:8553442 | G | A | 5 | a0001c0001t0002g0181 a0001c0001t0002g0183 a0001c0001t0002g0184 others(2): Show |
5 | HG00673.hp2 NA18943.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+4539G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553442 | |||||||
| chr3:8553472 | C | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0053 |
2 | HG01255.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.723+4569C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553472 | |||||||
| chr3:8553560 | A | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4657A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553560 | |||||||
| chr3:8553585 | A | C | 1 | a0001c0002t0041g0256 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.723+4682A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553585 | |||||||
| chr3:8553639 | C | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4736C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553639 | |||||||
| chr3:8553650 | G | A | 2 | a0001c0001t0026g0064 a0001c0001t0027g0092 |
2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.723+4747G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553650 | |||||||
| chr3:8553851 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4948A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553851 | |||||||
| chr3:8554011 | G | A | 1 | a0001c0001t0007g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.723+5108G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554011 | |||||||
| chr3:8554043 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.723+5140C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554043 | |||||||
| chr3:8554096 | G | A | 7 | a0001c0002t0003g0112 a0001c0002t0003g0166 a0001c0002t0011g0019 others(4): Show |
7 | HG00408.hp2 HG00597.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+5193G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554096 | |||||||
| chr3:8554305 | C | T | 1 | a0001c0001t0003g0165 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.723+5402C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554305 | |||||||
| chr3:8554364 | C | T | 2 | a0001c0002t0001g0244 a0006c0006t0001g0228 |
2 | HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.723+5461C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554364 | |||||||
| chr3:8554401 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+5498G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554401 | |||||||
| chr3:8554624 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+5721A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554624 | |||||||
| chr3:8554682 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+5779C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554682 | |||||||
| chr3:8554714 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.723+5811C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554714 | |||||||
| chr3:8554772 | G | A | 1 | a0001c0001t0022g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.723+5869G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554772 | |||||||
| chr3:8554910 | A | T | 2 | a0001c0002t0002g0236 a0001c0002t0002g0237 |
2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.723+6007A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554910 | |||||||
| chr3:8554912 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.723+6009C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554912 | |||||||
| chr3:8554943 | G | C | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.723+6040G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554943 | |||||||
| chr3:8555071 | C | T | 4 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0003g0263 others(1): Show |
4 | NA18956.hp2 NA18965.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+6168C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555071 | |||||||
| chr3:8555073 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+6170C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555073 | |||||||
| chr3:8555097 | T | C | 1 | a0001c0001t0012g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.723+6194T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555097 | |||||||
| chr3:8555164 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+6261C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555164 | |||||||
| chr3:8555193 | C | T | 3 | a0001c0001t0005g0192 a0001c0001t0005g0201 a0001c0001t0005g0239 |
3 | HG02622.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.723+6290C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555193 | |||||||
| chr3:8555419 | A | G | 2 | a0001c0001t0029g0289 a0001c0002t0041g0256 |
2 | HG01074.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.723+6516A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555419 | |||||||
| chr3:8555495 | C | A | 1 | a0001c0001t0001g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.723+6592C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555495 | |||||||
| chr3:8555624 | CT | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+6730delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555624 | ||||||
| chr3:8555712 | C | A | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+6809C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555712 | |||||||
| chr3:8555716 | C | CT | 42 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0155 others(39): Show |
45 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.723+6837dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | ||||||
| chr3:8555716 | C | CTT | 9 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 others(6): Show |
9 | HG01169.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+6836_723+6837d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | ||||||
| chr3:8555716 | C | CTTT | 41 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(38): Show |
43 | HG00597.hp2 HG01069.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.723+6835_723+6837d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | ||||||
| chr3:8555716 | CT | C | 8 | a0001c0001t0001g0262 a0001c0001t0003g0156 a0001c0001t0003g0288 others(5): Show |
8 | HG00609.hp1 HG01070.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+6837delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | ||||||
| chr3:8555743 | G | C | 1 | a0001c0001t0043g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.723+6840G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555743 | |||||||
| chr3:8555775 | G | C | 1 | a0001c0001t0055g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.723+6872G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555775 | |||||||
| chr3:8555849 | C | T | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.723+6946C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555849 | |||||||
| chr3:8555926 | A | G | 4 | a0001c0002t0002g0191 a0001c0002t0004g0078 a0001c0002t0004g0225 others(1): Show |
4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+7023A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555926 | |||||||
| chr3:8555998 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.723+7095G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555998 | |||||||
| chr3:8556085 | G | T | 70 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0120 others(67): Show |
73 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.723+7182G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556085 | |||||||
| chr3:8556361 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723+7458A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556361 | |||||||
| chr3:8556480 | A | C | 2 | a0001c0001t0017g0229 a0001c0001t0017g0230 |
2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.723+7577A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556480 | |||||||
| chr3:8556481 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723+7578A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556481 | |||||||
| chr3:8556550 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.723+7647G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556550 | |||||||
| chr3:8556624 | C | T | 2 | a0001c0002t0001g0244 a0006c0006t0001g0228 |
2 | HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.723+7721C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556624 | |||||||
| chr3:8556644 | A | G | 75 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0120 others(72): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.723+7741A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556644 | |||||||
| chr3:8556984 | G | C | 75 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0120 others(72): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.723+8081G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556984 | |||||||
| chr3:8557004 | C | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0294 a0001c0001t0002g0116 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+8101C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557004 | |||||||
| chr3:8557251 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.724-8181A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557251 | |||||||
| chr3:8557597 | C | A | 7 | a0001c0001t0001g0086 a0001c0001t0004g0226 a0001c0001t0021g0083 others(4): Show |
7 | HG01169.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.724-7835C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557597 | |||||||
| chr3:8557603 | A | C | 2 | a0001c0001t0002g0181 a0001c0001t0016g0180 |
2 | HG00673.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.724-7829A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557603 | |||||||
| chr3:8557737 | G | A | 2 | a0001c0001t0026g0064 a0001c0001t0027g0092 |
2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.724-7695G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557737 | |||||||
| chr3:8557827 | G | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0250 others(21): Show |
25 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.724-7605G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557827 | |||||||
| chr3:8558038 | G | C | 71 | a0001c0001t0001g0033 a0001c0001t0001g0286 a0001c0001t0002g0009 others(68): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.724-7394G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558038 | |||||||
| chr3:8558228 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.724-7204G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558228 | |||||||
| chr3:8558247 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.724-7185C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558247 | |||||||
| chr3:8558324 | T | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): Show |
62 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.724-7108T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558324 | |||||||
| chr3:8558329 | G | T | 2 | a0001c0001t0034g0238 a0001c0001t0040g0205 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-7103G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558329 | |||||||
| chr3:8558540 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.724-6892G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558540 | |||||||
| chr3:8558707 | T | C | 1 | a0001c0001t0042g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.724-6725T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558707 | |||||||
| chr3:8558823 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-6609T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558823 | |||||||
| chr3:8558950 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
57 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.724-6482C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558950 | |||||||
| chr3:8558982 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.724-6450C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558982 | |||||||
| chr3:8559021 | A | AC | 55 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
57 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.724-6410dupC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8559021 | ||||||
| chr3:8559059 | G | A | 21 | a0001c0001t0001g0017 a0001c0001t0001g0120 a0001c0001t0001g0294 others(18): Show |
22 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.724-6373G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559059 | |||||||
| chr3:8559062 | C | CCTCCA | 4 | a0001c0001t0001g0086 a0001c0001t0017g0229 a0001c0001t0017g0230 others(1): Show |
4 | HG02523.hp1 HG03453.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-6369_724-6365d others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8559062 | ||||||
| chr3:8559285 | G | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0294 a0001c0001t0002g0227 others(15): Show |
19 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.724-6147G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559285 | |||||||
| chr3:8559353 | C | T | 4 | a0001c0001t0004g0292 a0001c0001t0014g0296 a0001c0001t0052g0295 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-6079C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559353 | |||||||
| chr3:8559394 | A | G | 2 | a0001c0002t0004g0225 a0001c0002t0050g0193 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.724-6038A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559394 | |||||||
| chr3:8559422 | C | CCACAATC others(697): Show |
7 | a0001c0001t0001g0086 a0001c0001t0001g0186 a0001c0001t0001g0189 others(4): Show |
7 | HG02486.hp1 HG02523.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.724-5785_724-5784i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8559422 | ||||||
| chr3:8559574 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0003g0187 a0001c0001t0014g0188 |
3 | HG02717.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.724-5858T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559574 | |||||||
| chr3:8559648 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(97): Show |
102 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.724-5784A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559648 | |||||||
| chr3:8559677 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.724-5755C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559677 | |||||||
| chr3:8559723 | A | G | 1 | a0001c0001t0036g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724-5709A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559723 | |||||||
| chr3:8559793 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.724-5639C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559793 | |||||||
| chr3:8559878 | T | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0294 a0001c0001t0002g0227 others(15): Show |
19 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.724-5554T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559878 | |||||||
| chr3:8559927 | T | C | 36 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(33): Show |
36 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.724-5505T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559927 | |||||||
| chr3:8560060 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.724-5372A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560060 | |||||||
| chr3:8560078 | A | AATTAGAA others(697): Show |
1 | a0001c0001t0035g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.724-5304_724-5303i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8560078 | ||||||
| chr3:8560078 | A | AATTAGAA others(697): Show |
3 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0028g0176 |
3 | NA18965.hp1 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.724-5304_724-5303i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8560078 | ||||||
| chr3:8560078 | A | AATTAGAA others(697): Show |
28 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(25): Show |
28 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.724-5304_724-5303i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8560078 | ||||||
| chr3:8560078 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
70 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.724-5354A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560078 | |||||||
| chr3:8560126 | G | T | 5 | a0001c0001t0001g0155 a0001c0001t0001g0169 a0001c0001t0001g0231 others(2): Show |
5 | NA18979.hp2 NA18994.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-5306G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560126 | |||||||
| chr3:8560190 | C | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(118): Show |
124 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.724-5242C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560190 | |||||||
| chr3:8560490 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0021g0083 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.724-4942G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560490 | |||||||
| chr3:8560758 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.724-4674C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560758 | |||||||
| chr3:8560790 | G | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): Show |
60 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.724-4642G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560790 | |||||||
| chr3:8561026 | T | C | 1 | a0001c0001t0003g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.724-4406T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561026 | |||||||
| chr3:8561215 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.724-4217C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561215 | |||||||
| chr3:8561253 | A | G | 32 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(29): Show |
32 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.724-4179A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561253 | |||||||
| chr3:8561346 | A | G | 3 | a0001c0001t0003g0044 a0001c0001t0003g0283 a0001c0001t0049g0285 |
3 | HG01192.hp2 HG01255.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.724-4086A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561346 | |||||||
| chr3:8561356 | A | G | 1 | a0001c0001t0036g0243 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724-4076A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561356 | |||||||
| chr3:8561381 | GT | G | 9 | a0001c0001t0001g0086 a0001c0001t0002g0141 a0001c0001t0003g0036 others(6): Show |
9 | HG01167.hp1 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.724-4034delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8561381 | ||||||
| chr3:8561381 | GTT | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
113 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.724-4035_724-4034d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8561381 | ||||||
| chr3:8561389 | T | G | 5 | a0001c0001t0003g0266 a0001c0001t0003g0280 a0001c0001t0003g0287 others(2): Show |
5 | HG00642.hp2 HG00738.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-4043T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561389 | |||||||
| chr3:8561412 | A | T | 2 | a0001c0001t0034g0238 a0001c0001t0040g0205 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-4020A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561412 | |||||||
| chr3:8561544 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.724-3888C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561544 | |||||||
| chr3:8561545 | G | A | 1 | a0003c0010t0002g0119 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.724-3887G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561545 | |||||||
| chr3:8561557 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(229): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.724-3875T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561557 | |||||||
| chr3:8561573 | C | T | 1 | a0001c0008t0002g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.724-3859C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561573 | |||||||
| chr3:8561674 | C | T | 1 | a0001c0001t0012g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.724-3758C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561674 | |||||||
| chr3:8561708 | A | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0028g0176 |
3 | NA18965.hp1 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.724-3724A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561708 | |||||||
| chr3:8561797 | C | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-3635C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561797 | |||||||
| chr3:8561871 | C | CATT | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-3559_724-3558i others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8561871 | ||||||
| chr3:8561986 | G | A | 2 | a0001c0001t0003g0272 a0001c0001t0003g0288 |
2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.724-3446G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561986 | |||||||
| chr3:8561988 | T | G | 1 | a0001c0001t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.724-3444T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561988 | |||||||
| chr3:8562193 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 |
3 | HG02486.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724-3239A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562193 | |||||||
| chr3:8562250 | T | C | 45 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(42): Show |
45 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.724-3182T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562250 | |||||||
| chr3:8562330 | A | C | 1 | a0001c0001t0002g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.724-3102A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562330 | |||||||
| chr3:8562393 | T | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(99): Show |
104 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.724-3039T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562393 | |||||||
| chr3:8562496 | C | T | 1 | a0001c0002t0001g0244 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.724-2936C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562496 | |||||||
| chr3:8562683 | C | A | 1 | a0001c0002t0001g0032 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.724-2749C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562683 | |||||||
| chr3:8562768 | A | G | 32 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(29): Show |
32 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.724-2664A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562768 | |||||||
| chr3:8562898 | G | C | 2 | a0001c0001t0001g0086 a0001c0001t0021g0083 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.724-2534G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562898 | |||||||
| chr3:8562964 | G | T | 2 | a0001c0001t0017g0229 a0001c0001t0017g0230 |
2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.724-2468G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562964 | |||||||
| chr3:8563033 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.724-2399T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563033 | |||||||
| chr3:8563278 | T | C | 1 | a0001c0001t0051g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.724-2154T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563278 | |||||||
| chr3:8563289 | C | G | 2 | a0001c0001t0034g0238 a0001c0001t0040g0205 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-2143C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563289 | |||||||
| chr3:8563381 | C | G | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-2051C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563381 | |||||||
| chr3:8563459 | G | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(113): Show |
119 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.724-1973G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563459 | |||||||
| chr3:8563608 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.724-1824G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563608 | |||||||
| chr3:8563613 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.724-1819G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563613 | |||||||
| chr3:8563645 | T | C | 1 | a0007c0012t0001g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.724-1787T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563645 | |||||||
| chr3:8563683 | A | G | 1 | a0004c0011t0001g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.724-1749A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563683 | |||||||
| chr3:8563711 | C | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 |
3 | HG02486.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724-1721C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563711 | |||||||
| chr3:8563884 | A | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(53): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.724-1548A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563884 | |||||||
| chr3:8563885 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.724-1547C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563885 | |||||||
| chr3:8564027 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0206 |
3 | HG02486.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724-1405G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564027 | |||||||
| chr3:8564214 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.724-1218T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564214 | |||||||
| chr3:8564216 | C | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0186 a0001c0001t0001g0189 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-1216C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564216 | |||||||
| chr3:8564262 | A | ATAT | 3 | a0001c0001t0001g0013 a0001c0001t0014g0296 a0001c0001t0052g0295 |
3 | HG01884.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.724-1153_724-1151d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8564262 | ||||||
| chr3:8564533 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.724-899A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564533 | |||||||
| chr3:8564667 | A | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-765A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564667 | |||||||
| chr3:8564673 | A | G | 1 | a0001c0001t0004g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.724-759A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564673 | |||||||
| chr3:8564745 | T | G | 3 | a0001c0001t0004g0226 a0001c0001t0034g0238 a0001c0001t0040g0205 |
3 | HG02258.hp2 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-687T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564745 | |||||||
| chr3:8565153 | A | G | 59 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0110 others(56): Show |
61 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.724-279A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8565153 | |||||||
| chr3:8565245 | G | A | 2 | a0001c0001t0021g0083 a0001c0001t0040g0205 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.724-187G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8565245 | |||||||
| chr3:8565307 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.724-125C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8565307 | |||||||
| chr3:8565681 | T | C | 1 | a0003c0010t0002g0119 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.939+34T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565681 | |||||||
| chr3:8565847 | G | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
145 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.939+200G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565847 | |||||||
| chr3:8565953 | T | A | 1 | a0001c0001t0003g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.939+306T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565953 | |||||||
| chr3:8565968 | T | G | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.939+321T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565968 | |||||||
| chr3:8566266 | GTAACTC | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0001g0102 others(10): Show |
14 | HG00597.hp2 HG02080.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.939+623_939+628del others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 8566266 | ||||||
| chr3:8566331 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.939+684C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566331 | |||||||
| chr3:8566561 | T | G | 5 | a0001c0001t0012g0211 a0001c0001t0012g0248 a0001c0001t0014g0188 others(2): Show |
5 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.940-879T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566561 | |||||||
| chr3:8566652 | A | G | 1 | a0001c0001t0034g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.940-788A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566652 | |||||||
| chr3:8566743 | A | C | 5 | a0001c0001t0007g0212 a0001c0001t0007g0240 a0001c0001t0007g0270 others(2): Show |
5 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-697A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566743 | |||||||
| chr3:8566817 | T | G | 2 | a0001c0001t0003g0167 a0001c0001t0003g0168 |
2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.940-623T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566817 | |||||||
| chr3:8567023 | G | A | 1 | a0001c0001t0029g0289 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.940-417G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567023 | |||||||
| chr3:8567220 | A | AT | 7 | a0001c0001t0007g0212 a0001c0001t0007g0240 a0001c0001t0007g0270 others(4): Show |
7 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-212dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 8567220 | ||||||
| chr3:8567234 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.940-206G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567234 | |||||||
| chr3:8567385 | G | A | 95 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0011 others(92): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.940-55G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567385 | |||||||
| chr3:8567395 | A | G | 7 | a0001c0001t0007g0212 a0001c0001t0007g0240 a0001c0001t0007g0270 others(4): Show |
7 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-45A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567395 | |||||||
| chr3:8567430 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-10C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567430 |