Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91807 |
| ensemblid | ENSG00000140795.13 |
| hgncid | 29826 |
| symbol | MYLK3 |
| name | myosin light chain kinase 3 |
| refseq_nuc | NM_182493.3 |
| refseq_prot | NP_872299.2 |
| ensembl_nuc | ENST00000394809.9 |
| ensembl_prot | ENSP00000378288.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 46702282 |
| end | 46748344 |
| strand | - |
| ver | v1.2 |
| region | chr16:46702282-46748344 |
| region5000 | chr16:46697282-46753344 |
| regionname0 | MYLK3_chr16_46702282_46748344 |
| regionname5000 | MYLK3_chr16_46697282_46753344 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 819 | 127 | 66 | 27 | 22 | 4 | 7 | 17 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0002 | 0/1 | 819 | 85 | 9 | 20 | 22 | 6 | 27 | 19 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0003 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0004 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0005 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0006 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0007 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| a0008 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | MSGTS others(814): Show |
chr16 | 46697282 | 46753344 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2457 | 125 | 64 | 27 | 22 | 4 | 7 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0001c0007 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0001c0011 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0002c0002 | 0/1 | 2457 | 82 | 9 | 18 | 22 | 5 | 27 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0002c0003 | 0/0 | 2457 | 3 | 0 | 2 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0003c0008 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0004c0004 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0005c0009 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0006c0006 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0007c0005 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 | ||
| a0008c0010 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ATGTC others(2452): Show |
chr16 | 46697282 | 46753344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8032 | 66 | 29 | 13 | 20 | 1 | 3 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0002 | 0/0 | 8033 | 40 | 21 | 12 | 1 | 3 | 3 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0003 | 1/0 | 8033 | 8 | 6 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0005 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0006 | 0/0 | 8033 | 3 | 3 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0007 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0008 | 0/0 | 8033 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0010 | 0/0 | 8033 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0011 | 0/0 | 8032 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0015 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0001c0001t0017 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0001c0007t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0001c0011t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0001 | 0/1 | 8032 | 68 | 9 | 18 | 18 | 5 | 17 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0004 | 0/0 | 8032 | 5 | 0 | 0 | 0 | 0 | 5 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0005 | 0/0 | 8032 | 2 | 0 | 0 | 2 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0007 | 0/0 | 8033 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0009 | 0/0 | 8032 | 2 | 0 | 0 | 0 | 0 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0012 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0013 | 0/0 | 8032 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0014 | 0/0 | 8032 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0002t0016 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0002c0003t0001 | 0/0 | 8032 | 3 | 0 | 2 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0003c0008t0001 | 0/0 | 8032 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0004c0004t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0005c0009t0018 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8028): Show |
chr16 | 46697282 | 46753344 |
| a0006c0006t0001 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0007c0005t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| a0008c0010t0001 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | ACACA others(8027): Show |
chr16 | 46697282 | 46753344 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0001 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0008g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0011g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0011t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0002 | 0/0 | 6 | 0 | 1 | 1 | 2 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0008 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0009g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0009g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0013g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0014g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0016g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0003t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0003c0008t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0004c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0005c0009t0018g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0006c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0007c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0008c0010t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0120 | EUR | FIN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0020 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01074 | hp1 | a0003 | c0008 | t0001 | g0071 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0127 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0009 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0107 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02572 | hp1 | a0001 | c0011 | t0001 | g0149 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0016 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02683 | hp1 | a0002 | c0002 | t0014 | g0141 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02698 | hp2 | a0002 | c0002 | t0009 | g0180 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02717 | hp1 | a0005 | c0009 | t0018 | g0090 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02738 | hp1 | a0002 | c0002 | t0009 | g0181 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02970 | hp2 | a0001 | c0007 | t0001 | g0051 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0179 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0032 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0174 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03654 | hp2 | a0002 | c0002 | t0004 | g0133 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03669 | hp1 | a0002 | c0002 | t0013 | g0103 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04115 | hp1 | a0002 | c0002 | t0007 | g0052 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04115 | hp2 | a0002 | c0002 | t0004 | g0060 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04184 | hp2 | a0002 | c0002 | t0004 | g0134 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0135 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04204 | hp2 | a0002 | c0002 | t0004 | g0064 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0130 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18998 | hp1 | a0002 | c0002 | t0016 | g0123 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19001 | hp2 | a0006 | c0006 | t0001 | g0086 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19043 | hp1 | a0007 | c0005 | t0001 | g0022 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19076 | hp2 | a0008 | c0010 | t0001 | g0073 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19080 | hp1 | a0002 | c0002 | t0012 | g0063 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19088 | hp1 | a0002 | c0002 | t0005 | g0131 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | ASW | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0122 | EUR | TSI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0091 | REF | REF | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0045 | REF | REF | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46721148 | T | C | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1960A>G | p.Ile654Val | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/13 | 2111/8033 | 1960/2460 | 654/819 | chr16 | 46721148 | |||
| chr16:46721192 | G | A | 1 | a0005 | 1 | HG02717.hp1 | missense_variant&splice_region_variant | MODERATE | c.1916C>T | p.Pro639Leu | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/13 | 2067/8033 | 1916/2460 | 639/819 | chr16 | 46721192 | |||
| chr16:46729124 | T | C | 1 | a0008 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1672A>G | p.Lys558Glu | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/13 | 1823/8033 | 1672/2460 | 558/819 | chr16 | 46729124 | |||
| chr16:46730662 | C | G | 1 | a0008 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1499G>C | p.Arg500Pro | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/13 | 1650/8033 | 1499/2460 | 500/819 | chr16 | 46730662 | |||
| chr16:46730663 | G | C | 1 | a0008 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1498C>G | p.Arg500Gly | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/13 | 1649/8033 | 1498/2460 | 500/819 | chr16 | 46730663 | |||
| chr16:46732367 | C | G | 1 | a0006 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1303G>C | p.Asp435His | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/13 | 1454/8033 | 1303/2460 | 435/819 | chr16 | 46732367 | |||
| chr16:46732502 | C | T | 1 | a0007 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1168G>A | p.Gly390Arg | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/13 | 1319/8033 | 1168/2460 | 390/819 | chr16 | 46732502 | |||
| chr16:46740087 | C | A | 1 | a0002 | 84 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(81): Show |
missense_variant | MODERATE | c.538G>T | p.Val180Leu | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/13 | 689/8033 | 538/2460 | 180/819 | chr16 | 46740087 | |||
| chr16:46747965 | C | T | 1 | a0004 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.229G>A | p.Gly77Arg | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/13 | 380/8033 | 229/2460 | 77/819 | chr16 | 46747965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46710684 | C | T | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2220G>A | p.Ser740Ser | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/13 | 2371/8033 | 2220/2460 | 740/819 | chr16 | 46710684 | |||
| chr16:46729125 | C | T | 1 | a0008c0010 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.1671G>A | p.Val557Val | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/13 | 1822/8033 | 1671/2460 | 557/819 | chr16 | 46729125 | |||
| chr16:46730673 | A | G | 1 | a0002c0003 | 3 | HG01109.hp2 HG01243.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.1488T>C | p.Pro496Pro | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/13 | 1639/8033 | 1488/2460 | 496/819 | chr16 | 46730673 | |||
| chr16:46732650 | T | C | 1 | a0001c0011 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1020A>G | p.Gln340Gln | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/13 | 1171/8033 | 1020/2460 | 340/819 | chr16 | 46732650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46702292 | G | A | 1 | a0002c0002t0014 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5412C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 5412 | chr16 | 46702292 | ||||||
| chr16:46702351 | C | T | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(20): Show |
162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*5353G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 5353 | chr16 | 46702351 | ||||||
| chr16:46702956 | TA | T | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(18): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*4747delT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 4747 | chr16 | 46702956 | ||||||
| chr16:46703598 | T | C | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(24): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*4106A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 4106 | chr16 | 46703598 | ||||||
| chr16:46704397 | T | C | 1 | a0001c0001t0015 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3307A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3307 | chr16 | 46704397 | ||||||
| chr16:46704506 | T | C | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(21): Show |
164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*3198A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3198 | chr16 | 46704506 | ||||||
| chr16:46704536 | C | G | 1 | a0002c0002t0004 | 5 | HG03654.hp2 HG04115.hp2 HG04184.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3168G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3168 | chr16 | 46704536 | ||||||
| chr16:46704657 | G | A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*3047C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3047 | chr16 | 46704657 | ||||||
| chr16:46705224 | C | T | 1 | a0002c0002t0013 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2480G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 2480 | chr16 | 46705224 | ||||||
| chr16:46705476 | C | T | 2 | a0001c0001t0005 a0002c0002t0005 |
3 | NA18942.hp1 NA18968.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2228G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 2228 | chr16 | 46705476 | ||||||
| chr16:46705628 | A | T | 1 | a0002c0002t0012 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 2076 | chr16 | 46705628 | ||||||
| chr16:46705991 | G | A | 1 | a0001c0001t0006 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1713C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1713 | chr16 | 46705991 | ||||||
| chr16:46706067 | T | C | 1 | a0001c0001t0006 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1637A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1637 | chr16 | 46706067 | ||||||
| chr16:46706361 | T | G | 1 | a0002c0002t0016 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1343A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1343 | chr16 | 46706361 | ||||||
| chr16:46706442 | C | A | 3 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 |
42 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1262G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1262 | chr16 | 46706442 | ||||||
| chr16:46706688 | G | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(24): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1016C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1016 | chr16 | 46706688 | ||||||
| chr16:46706970 | G | T | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*734C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 734 | chr16 | 46706970 | ||||||
| chr16:46707131 | C | G | 1 | a0001c0001t0011 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 573 | chr16 | 46707131 | ||||||
| chr16:46707133 | T | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*571A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 571 | chr16 | 46707133 | ||||||
| chr16:46707358 | G | A | 1 | a0005c0009t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 346 | chr16 | 46707358 | ||||||
| chr16:46707488 | C | T | 1 | a0001c0001t0010 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*216G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 216 | chr16 | 46707488 | ||||||
| chr16:46748335 | T | C | 1 | a0002c0002t0009 | 2 | HG02698.hp2 HG02738.hp1 |
5_prime_UTR_variant | MODIFIER | c.-142A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/13 | 142 | chr16 | 46748335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46707951 | G | A | 5 | a0002c0002t0001g0058 a0002c0002t0001g0065 a0002c0002t0001g0137 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401-188C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46707951 | |||||||
| chr16:46707953 | A | ATGAATAT others(3): Show |
5 | a0002c0002t0001g0058 a0002c0002t0001g0065 a0002c0002t0001g0137 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401-191_2401-190i others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46707953 | |||||||
| chr16:46709214 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2400+325C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709214 | |||||||
| chr16:46709416 | T | C | 1 | a0002c0002t0001g0100 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2400+123A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709416 | |||||||
| chr16:46709443 | G | GA | 26 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0053 others(23): Show |
35 | HG00099.hp1 HG00621.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2400+95dupT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709443 | |||||||
| chr16:46709446 | A | C | 1 | a0001c0001t0002g0029 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2400+93T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709446 | |||||||
| chr16:46709763 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(137): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2268-92C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46709763 | |||||||
| chr16:46709796 | A | G | 2 | a0001c0001t0001g0076 a0002c0002t0001g0055 |
2 | NA18955.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2268-125T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46709796 | |||||||
| chr16:46709857 | G | A | 1 | a0001c0001t0002g0026 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2268-186C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46709857 | |||||||
| chr16:46710135 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0005c0009t0018g0090 |
3 | HG01884.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2268-464A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46710135 | |||||||
| chr16:46710926 | T | C | 2 | a0001c0001t0001g0023 a0007c0005t0001g0022 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2115-137A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46710926 | |||||||
| chr16:46711715 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2115-926G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711715 | |||||||
| chr16:46711807 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2114+841A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711807 | |||||||
| chr16:46711962 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2114+686G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711962 | |||||||
| chr16:46711989 | AT | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(160): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2114+658delA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711989 | |||||||
| chr16:46711989 | ATT | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0176 a0001c0001t0002g0039 others(2): Show |
5 | HG02818.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2114+657_2114+658d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711989 | |||||||
| chr16:46712172 | G | T | 1 | a0002c0002t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2114+476C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46712172 | |||||||
| chr16:46713157 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0002g0034 |
2 | HG01106.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1986-381G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713157 | |||||||
| chr16:46713199 | C | CT | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(158): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1986-424dupA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713199 | |||||||
| chr16:46713245 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1986-469A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713245 | |||||||
| chr16:46713346 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1986-570G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713346 | |||||||
| chr16:46713978 | A | T | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1986-1202T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713978 | |||||||
| chr16:46714007 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986-1231A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714007 | |||||||
| chr16:46714085 | C | T | 1 | a0002c0002t0013g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1986-1309G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714085 | |||||||
| chr16:46714416 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1986-1640C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714416 | |||||||
| chr16:46714479 | C | T | 165 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(162): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1986-1703G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714479 | |||||||
| chr16:46714481 | C | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(165): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1986-1705G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714481 | |||||||
| chr16:46714574 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1986-1798C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714574 | |||||||
| chr16:46714656 | C | T | 1 | a0002c0002t0001g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1986-1880G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714656 | |||||||
| chr16:46714703 | A | C | 1 | a0002c0002t0001g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1986-1927T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714703 | |||||||
| chr16:46715077 | C | T | 1 | a0002c0002t0014g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1986-2301G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715077 | |||||||
| chr16:46715078 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1986-2302C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715078 | |||||||
| chr16:46715286 | G | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986-2510C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715286 | |||||||
| chr16:46715291 | C | G | 28 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0053 others(25): Show |
37 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1986-2515G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715291 | |||||||
| chr16:46715301 | A | C | 1 | a0002c0002t0001g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1986-2525T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715301 | |||||||
| chr16:46715462 | T | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1986-2686A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715462 | |||||||
| chr16:46715500 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1986-2724C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715500 | |||||||
| chr16:46715947 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1986-3171T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715947 | |||||||
| chr16:46716017 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1986-3241C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716017 | |||||||
| chr16:46716033 | G | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1986-3257C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716033 | |||||||
| chr16:46716045 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0025 a0001c0001t0002g0039 |
4 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986-3269G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716045 | |||||||
| chr16:46716077 | C | T | 1 | a0005c0009t0018g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1986-3301G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716077 | |||||||
| chr16:46716155 | T | C | 1 | a0001c0001t0008g0011 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1986-3379A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716155 | |||||||
| chr16:46716489 | GTA | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0067 others(17): Show |
21 | HG00642.hp2 HG01069.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1986-3715_1986-371 others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716489 | |||||||
| chr16:46716495 | ATATG | A | 81 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(78): Show |
91 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1986-3723_1986-372 others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | |||||||
| chr16:46716495 | ATATGTG | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0050 others(31): Show |
40 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1986-3725_1986-372 others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | |||||||
| chr16:46716495 | ATATGTGT others(1): Show |
A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0004c0004t0001g0016 |
4 | HG00621.hp1 HG02129.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986-3727_1986-372 others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | |||||||
| chr16:46716495 | ATATGTGT others(3): Show |
A | 2 | a0002c0002t0001g0096 a0002c0002t0005g0131 |
2 | HG02602.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1986-3729_1986-372 others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | |||||||
| chr16:46716497 | A | ATG | 6 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0010 others(3): Show |
11 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1986-3723_1986-372 others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716497 | |||||||
| chr16:46716497 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0003g0042 a0002c0002t0013g0103 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986-3721T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716497 | |||||||
| chr16:46716863 | T | C | 1 | a0002c0002t0009g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1986-4087A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716863 | |||||||
| chr16:46717530 | T | TC | 11 | a0001c0001t0001g0049 a0001c0001t0002g0004 a0001c0001t0002g0005 others(8): Show |
18 | HG00099.hp2 HG00733.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1985+3592dupG | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46717530 | |||||||
| chr16:46717540 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1985+3583T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46717540 | |||||||
| chr16:46717556 | G | A | 2 | a0001c0001t0001g0089 a0001c0007t0001g0051 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1985+3567C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46717556 | |||||||
| chr16:46718208 | A | T | 2 | a0002c0002t0001g0116 a0002c0002t0001g0117 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1985+2915T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718208 | |||||||
| chr16:46718408 | C | T | 2 | a0002c0002t0001g0125 a0002c0002t0001g0142 |
2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1985+2715G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718408 | |||||||
| chr16:46718430 | G | A | 1 | a0002c0002t0001g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1985+2693C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718430 | |||||||
| chr16:46718437 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1985+2686T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718437 | |||||||
| chr16:46718522 | G | C | 28 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0053 others(25): Show |
37 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1985+2601C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718522 | |||||||
| chr16:46719053 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0110 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1985+2070C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719053 | |||||||
| chr16:46719196 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1985+1927C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719196 | |||||||
| chr16:46719321 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1985+1802C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719321 | |||||||
| chr16:46719326 | CA | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0178 others(4): Show |
7 | HG01256.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1985+1796delT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719326 | |||||||
| chr16:46719345 | A | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0168 |
2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1985+1778T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719345 | |||||||
| chr16:46719376 | C | T | 1 | a0002c0002t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1985+1747G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719376 | |||||||
| chr16:46720311 | C | CA | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0005c0009t0018g0090 |
3 | HG01884.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1985+811dupT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46720311 | |||||||
| chr16:46720381 | G | C | 1 | a0002c0002t0001g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1985+742C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46720381 | |||||||
| chr16:46720400 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1985+723C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46720400 | |||||||
| chr16:46721073 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1985+50G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46721073 | |||||||
| chr16:46721301 | C | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1915-108G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721301 | |||||||
| chr16:46721405 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1915-212G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721405 | |||||||
| chr16:46721448 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1915-255A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721448 | |||||||
| chr16:46721573 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1915-380C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721573 | |||||||
| chr16:46721593 | G | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1915-400C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721593 | |||||||
| chr16:46721858 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1915-665T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721858 | |||||||
| chr16:46722077 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1915-884G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46722077 | |||||||
| chr16:46722718 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1915-1525C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46722718 | |||||||
| chr16:46722940 | G | A | 2 | a0002c0002t0001g0094 a0002c0002t0007g0052 |
2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1915-1747C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46722940 | |||||||
| chr16:46723207 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1915-2014C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723207 | |||||||
| chr16:46723589 | A | C | 1 | a0002c0002t0001g0119 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1915-2396T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723589 | |||||||
| chr16:46723616 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1915-2423A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723616 | |||||||
| chr16:46723650 | C | CT | 137 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(134): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1915-2458dupA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723650 | |||||||
| chr16:46723650 | C | CTT | 28 | a0001c0001t0001g0083 a0001c0011t0001g0149 a0002c0002t0001g0059 others(25): Show |
28 | HG00738.hp1 HG01106.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.1915-2459_1915-245 others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723650 | |||||||
| chr16:46723849 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0136 a0001c0007t0001g0051 |
3 | HG02818.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1915-2656T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723849 | |||||||
| chr16:46723892 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1915-2699C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723892 | |||||||
| chr16:46723943 | C | A | 1 | a0001c0001t0007g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1915-2750G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723943 | |||||||
| chr16:46724173 | T | G | 6 | a0001c0001t0001g0136 a0002c0002t0001g0065 a0002c0002t0001g0137 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1915-2980A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724173 | |||||||
| chr16:46724227 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+3009T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724227 | |||||||
| chr16:46724260 | T | C | 1 | a0002c0002t0001g0093 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1914+2976A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724260 | |||||||
| chr16:46724270 | A | G | 1 | a0001c0001t0006g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1914+2966T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724270 | |||||||
| chr16:46724938 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1914+2298G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724938 | |||||||
| chr16:46725176 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1914+2060A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725176 | |||||||
| chr16:46725565 | C | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1914+1671G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725565 | |||||||
| chr16:46725862 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1914+1374A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725862 | |||||||
| chr16:46725903 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1914+1333G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725903 | |||||||
| chr16:46725948 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(139): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1914+1288T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725948 | |||||||
| chr16:46726662 | AAAAAGAA others(6): Show |
A | 2 | a0001c0001t0001g0085 a0002c0002t0001g0061 |
2 | HG03654.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1914+561_1914+573d others(15): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726662 | |||||||
| chr16:46726663 | AAAAGAAA others(7): Show |
A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0023 others(17): Show |
21 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1914+559_1914+572d others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | |||||||
| chr16:46726663 | AAAAGAAA others(11): Show |
A | 9 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0173 others(6): Show |
9 | HG00558.hp2 HG01175.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1914+555_1914+572d others(20): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | |||||||
| chr16:46726663 | AAAAGAAA others(15): Show |
A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0152 others(4): Show |
7 | HG01361.hp1 HG02129.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1914+551_1914+572d others(24): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | |||||||
| chr16:46726663 | AAAAGAAA others(19): Show |
A | 1 | a0002c0002t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1914+547_1914+572d others(28): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | |||||||
| chr16:46726665 | AAGAAAGA others(3): Show |
A | 36 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0027 others(33): Show |
39 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1914+561_1914+570d others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726665 | |||||||
| chr16:46726669 | AAGAAAG | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0080 others(23): Show |
28 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1914+561_1914+566d others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726669 | |||||||
| chr16:46726673 | A | T | 2 | a0001c0001t0001g0068 a0002c0002t0001g0100 |
2 | NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1914+563T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726673 | |||||||
| chr16:46726673 | AAG | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0049 others(28): Show |
32 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1914+561_1914+562d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726673 | |||||||
| chr16:46726675 | G | GAA | 18 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0068 others(15): Show |
19 | HG00558.hp1 HG01175.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1914+560_1914+561i others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726675 | G | GAGAA | 16 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(13): Show |
21 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1914+557_1914+560d others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726675 | G | GAGAAAGA others(1): Show |
10 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(7): Show |
11 | HG01099.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1914+553_1914+560d others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726675 | G | GAGAAAGA others(5): Show |
3 | a0001c0001t0002g0005 a0001c0001t0010g0032 a0001c0001t0017g0179 |
4 | HG03139.hp2 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+549_1914+560d others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726675 | G | GAGAAAGA others(9): Show |
3 | a0001c0001t0002g0004 a0001c0001t0003g0017 a0001c0001t0003g0043 |
3 | HG01081.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1914+545_1914+560d others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726675 | GAGAA | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0030 a0001c0001t0006g0164 |
4 | HG02559.hp1 HG02809.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+557_1914+560d others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726675 | GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0006g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1914+549_1914+560d others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | |||||||
| chr16:46726733 | GA | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0162 a0001c0001t0002g0033 others(1): Show |
4 | HG00733.hp1 HG02280.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+502delT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726733 | |||||||
| chr16:46726737 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+499T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726737 | |||||||
| chr16:46726738 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+498C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726738 | |||||||
| chr16:46726744 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1914+492C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726744 | |||||||
| chr16:46726748 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1914+488C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726748 | |||||||
| chr16:46726752 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0161 |
2 | HG01884.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1914+484T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726752 | |||||||
| chr16:46726762 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+474T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726762 | |||||||
| chr16:46726763 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+473C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726763 | |||||||
| chr16:46726763 | G | GAAAGAGA others(14): Show |
1 | a0001c0001t0001g0162 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1914+472_1914+473i others(23): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726763 | |||||||
| chr16:46726803 | G | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(139): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1914+433C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726803 | |||||||
| chr16:46726883 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(135): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1914+353C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726883 | |||||||
| chr16:46727177 | G | A | 1 | a0002c0002t0004g0064 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1914+59C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46727177 | |||||||
| chr16:46727538 | T | G | 1 | a0002c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1773-161A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727538 | |||||||
| chr16:46727579 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1773-202A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727579 | |||||||
| chr16:46727609 | C | T | 1 | a0001c0001t0006g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1773-232G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727609 | |||||||
| chr16:46727813 | C | T | 1 | a0001c0001t0010g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1773-436G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727813 | |||||||
| chr16:46728446 | T | A | 1 | a0001c0001t0003g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1772+578A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46728446 | |||||||
| chr16:46728454 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1772+570G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46728454 | |||||||
| chr16:46728818 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1772+206C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46728818 | |||||||
| chr16:46729000 | G | A | 2 | a0001c0001t0008g0011 a0001c0001t0017g0179 |
3 | HG01884.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1772+24C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46729000 | |||||||
| chr16:46729004 | G | A | 8 | a0002c0002t0001g0061 a0002c0002t0001g0128 a0002c0002t0001g0129 others(5): Show |
8 | HG02698.hp2 HG02738.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1772+20C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46729004 | |||||||
| chr16:46729261 | C | T | 1 | a0002c0002t0007g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1663-128G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 6/12 | chr16 | 46729261 | |||||||
| chr16:46730042 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1569-355C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730042 | |||||||
| chr16:46730383 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1568+210C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730383 | |||||||
| chr16:46730439 | A | C | 1 | a0002c0002t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1568+154T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730439 | |||||||
| chr16:46730462 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(32): Show |
41 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1568+131G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730462 | |||||||
| chr16:46730488 | G | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1568+105C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730488 | |||||||
| chr16:46730570 | A | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1568+23T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730570 | |||||||
| chr16:46730980 | A | G | 2 | a0002c0002t0001g0053 a0002c0002t0001g0126 |
2 | HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1463-282T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46730980 | |||||||
| chr16:46730988 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1463-290C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46730988 | |||||||
| chr16:46731203 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1463-505T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731203 | |||||||
| chr16:46731207 | C | T | 1 | a0002c0002t0001g0054 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1463-509G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731207 | |||||||
| chr16:46731234 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(139): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1463-536C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731234 | |||||||
| chr16:46731351 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1463-653A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731351 | |||||||
| chr16:46731596 | AG | A | 1 | a0002c0003t0001g0009 | 3 | HG01109.hp2 HG01243.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1462+611delC | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731596 | |||||||
| chr16:46731771 | G | C | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1462+437C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731771 | |||||||
| chr16:46731789 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1462+419G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731789 | |||||||
| chr16:46731803 | C | T | 28 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0053 others(25): Show |
37 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1462+405G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731803 | |||||||
| chr16:46732850 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1002-182G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732850 | |||||||
| chr16:46732880 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1002-212C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732880 | |||||||
| chr16:46732956 | G | A | 1 | a0002c0002t0009g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1002-288C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732956 | |||||||
| chr16:46732979 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1002-311G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732979 | |||||||
| chr16:46733340 | G | A | 1 | a0001c0001t0006g0163 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-672C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733340 | |||||||
| chr16:46733452 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1002-784G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733452 | |||||||
| chr16:46733495 | C | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1002-827G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733495 | |||||||
| chr16:46733817 | G | A | 1 | a0002c0002t0016g0123 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1002-1149C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733817 | |||||||
| chr16:46734030 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1002-1362G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46734030 | |||||||
| chr16:46734123 | C | T | 1 | a0001c0001t0010g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1002-1455G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46734123 | |||||||
| chr16:46734702 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1002-2034T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46734702 | |||||||
| chr16:46735003 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1002-2335A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735003 | |||||||
| chr16:46735089 | C | T | 3 | a0002c0002t0001g0062 a0002c0002t0005g0130 a0002c0002t0005g0131 |
3 | NA18942.hp1 NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1002-2421G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735089 | |||||||
| chr16:46735354 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1001+2357G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735354 | |||||||
| chr16:46735355 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(23): Show |
45 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1001+2356C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735355 | |||||||
| chr16:46735368 | G | A | 1 | a0002c0002t0001g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1001+2343C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735368 | |||||||
| chr16:46735693 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1001+2018T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735693 | |||||||
| chr16:46735791 | G | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0056 others(4): Show |
9 | HG00621.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1001+1920C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735791 | |||||||
| chr16:46736044 | G | T | 1 | a0002c0002t0001g0113 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1001+1667C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736044 | |||||||
| chr16:46736055 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1001+1656A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736055 | |||||||
| chr16:46736366 | C | A | 2 | a0002c0002t0001g0137 a0002c0002t0001g0140 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1001+1345G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736366 | |||||||
| chr16:46736424 | C | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(135): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1001+1287G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736424 | |||||||
| chr16:46736485 | T | G | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001+1226A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736485 | |||||||
| chr16:46736868 | G | A | 3 | a0001c0001t0001g0089 a0001c0007t0001g0051 a0002c0002t0001g0059 |
3 | HG01106.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1001+843C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736868 | |||||||
| chr16:46736892 | G | GA | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001+818_1001+819i others(3): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736892 | |||||||
| chr16:46736893 | C | G | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001+818G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736893 | |||||||
| chr16:46737068 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1001+643G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737068 | |||||||
| chr16:46737300 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1001+411C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737300 | |||||||
| chr16:46737343 | G | A | 2 | a0001c0001t0001g0089 a0001c0007t0001g0051 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1001+368C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737343 | |||||||
| chr16:46737561 | C | A | 1 | a0001c0001t0017g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1001+150G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737561 | |||||||
| chr16:46737588 | C | T | 1 | a0001c0001t0011g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1001+123G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737588 | |||||||
| chr16:46738162 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.569-19C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738162 | |||||||
| chr16:46738187 | G | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569-44C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738187 | |||||||
| chr16:46738321 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0011g0020 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.569-178G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738321 | |||||||
| chr16:46738419 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.569-276A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738419 | |||||||
| chr16:46738516 | C | T | 1 | a0001c0001t0006g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.569-373G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738516 | |||||||
| chr16:46738517 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.569-374C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738517 | |||||||
| chr16:46738881 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569-738G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738881 | |||||||
| chr16:46739168 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(139): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.568+889T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739168 | |||||||
| chr16:46739212 | C | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.568+845G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739212 | |||||||
| chr16:46739233 | T | C | 1 | a0001c0001t0007g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.568+824A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739233 | |||||||
| chr16:46739482 | G | A | 1 | a0001c0001t0006g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.568+575C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739482 | |||||||
| chr16:46739549 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(139): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.568+508G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739549 | |||||||
| chr16:46739638 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.568+419A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739638 | |||||||
| chr16:46739840 | G | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.568+217C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739840 | |||||||
| chr16:46739935 | A | T | 1 | a0002c0002t0004g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.568+122T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739935 | |||||||
| chr16:46739937 | A | C | 2 | a0002c0002t0001g0093 a0002c0002t0001g0112 |
2 | HG02300.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.568+120T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739937 | |||||||
| chr16:46739985 | G | A | 1 | a0002c0002t0004g0064 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.568+72C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739985 | |||||||
| chr16:46740389 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.478-242G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740389 | |||||||
| chr16:46740520 | T | C | 1 | a0001c0001t0017g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478-373A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740520 | |||||||
| chr16:46740526 | T | C | 1 | a0002c0002t0001g0125 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.478-379A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740526 | |||||||
| chr16:46740530 | T | C | 1 | a0002c0002t0012g0063 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.478-383A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740530 | |||||||
| chr16:46740536 | C | CAT | 71 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(68): Show |
83 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.478-391_478-390dup others(2): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | |||||||
| chr16:46740536 | C | CATAT | 24 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(21): Show |
30 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.478-393_478-390dup others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | |||||||
| chr16:46740536 | C | CATATAT | 2 | a0001c0001t0001g0148 a0008c0010t0001g0073 |
2 | NA19076.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.478-395_478-390dup others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | |||||||
| chr16:46740536 | C | T | 1 | a0001c0011t0001g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-389G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | |||||||
| chr16:46740540 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.478-393A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740540 | |||||||
| chr16:46740551 | A | ATAT | 20 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(17): Show |
35 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.478-405_478-404ins others(3): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740551 | |||||||
| chr16:46740552 | T | TA | 5 | a0002c0002t0001g0055 a0002c0002t0001g0104 a0002c0002t0001g0105 others(2): Show |
5 | HG01167.hp1 HG01496.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-406_478-405ins others(1): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740552 | |||||||
| chr16:46740552 | T | TATA | 38 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0155 others(35): Show |
42 | HG00738.hp1 HG01074.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.478-406_478-405ins others(3): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740552 | |||||||
| chr16:46740552 | T | TATATA | 7 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
7 | HG02723.hp1 HG03471.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-406_478-405ins others(5): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740552 | |||||||
| chr16:46740553 | T | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(81): Show |
101 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.478-406A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740553 | |||||||
| chr16:46740554 | T | A | 14 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0089 others(11): Show |
14 | HG00280.hp1 HG02630.hp1 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-407A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740554 | |||||||
| chr16:46740555 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0157 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-408A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740555 | |||||||
| chr16:46740557 | T | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0178 a0004c0004t0001g0016 |
3 | HG02622.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.478-410A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740557 | |||||||
| chr16:46740766 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.478-619C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740766 | |||||||
| chr16:46740797 | C | T | 5 | a0002c0002t0001g0065 a0002c0002t0001g0137 a0002c0002t0001g0138 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-650G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740797 | |||||||
| chr16:46740847 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.478-700G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740847 | |||||||
| chr16:46740919 | C | T | 1 | a0001c0001t0008g0011 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.478-772G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740919 | |||||||
| chr16:46741030 | G | A | 4 | a0002c0002t0001g0061 a0002c0002t0001g0128 a0002c0002t0001g0129 others(1): Show |
4 | HG03490.hp1 HG03654.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-883C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741030 | |||||||
| chr16:46741037 | T | C | 3 | a0002c0002t0001g0062 a0002c0002t0005g0130 a0002c0002t0005g0131 |
3 | NA18942.hp1 NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.478-890A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741037 | |||||||
| chr16:46741150 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.478-1003C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741150 | |||||||
| chr16:46741638 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.478-1491T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741638 | |||||||
| chr16:46741731 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(139): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.478-1584C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741731 | |||||||
| chr16:46741770 | AT | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(155): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.478-1624delA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741770 | |||||||
| chr16:46741770 | ATT | A | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG01081.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1625_478-1624d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741770 | |||||||
| chr16:46741934 | C | G | 25 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-1787G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741934 | |||||||
| chr16:46741959 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.478-1812A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741959 | |||||||
| chr16:46742006 | T | G | 25 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-1859A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742006 | |||||||
| chr16:46742227 | G | GA | 101 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(98): Show |
113 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.478-2081dupT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742227 | |||||||
| chr16:46742244 | G | A | 1 | a0002c0002t0001g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478-2097C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742244 | |||||||
| chr16:46742323 | G | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(166): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.478-2176C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742323 | |||||||
| chr16:46742333 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.478-2186A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742333 | |||||||
| chr16:46742417 | G | A | 1 | a0002c0002t0012g0063 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.478-2270C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742417 | |||||||
| chr16:46742442 | G | GCACACAC others(9): Show |
1 | a0006c0006t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.478-2296_478-2295i others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742442 | |||||||
| chr16:46742443 | CAA | C | 4 | a0002c0002t0004g0064 a0002c0002t0004g0133 a0002c0002t0004g0134 others(1): Show |
4 | HG03654.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-2298_478-2297d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742443 | |||||||
| chr16:46742445 | A | AAC | 18 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0021 others(15): Show |
20 | HG00280.hp1 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACAC | 26 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(23): Show |
27 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACAC | 9 | a0001c0001t0001g0077 a0001c0001t0001g0156 a0001c0001t0001g0173 others(6): Show |
9 | HG02572.hp1 HG02602.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACACA others(1): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(31): Show |
34 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACACA others(3): Show |
20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0109 others(17): Show |
20 | HG00738.hp1 HG02630.hp1 HG02738.hp1 others(17): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACACA others(5): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0068 others(5): Show |
8 | HG01258.hp2 HG01361.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACACA others(7): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0148 a0008c0010t0001g0073 |
3 | HG04199.hp1 NA19076.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACACA others(9): Show |
1 | a0001c0001t0001g0085 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.478-2299_478-2298i others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | AACACACA others(11): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0084 |
2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(20): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | ACACACAC others(2): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0177 |
2 | HG01433.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(11): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0146 |
2 | HG00642.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(13): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | ACACACAC others(6): Show |
1 | a0002c0002t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.478-2299_478-2298i others(15): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | A | C | 4 | a0001c0001t0001g0003 a0002c0002t0001g0098 a0002c0002t0001g0143 others(1): Show |
4 | HG00558.hp1 HG02738.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-2298T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | AAAACAC | A | 5 | a0002c0002t0001g0065 a0002c0002t0001g0137 a0002c0002t0001g0138 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-2304_478-2299d others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | AAAACACA others(7): Show |
A | 1 | a0002c0002t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.478-2312_478-2299d others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742445 | AAAACACA others(9): Show |
A | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.478-2314_478-2299d others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | |||||||
| chr16:46742447 | A | AACACACA others(9): Show |
1 | a0005c0009t0018g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478-2316_478-2301d others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | A | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(120): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.478-2300T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | AACACAC | A | 5 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0047 others(2): Show |
5 | HG02109.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-2306_478-2301d others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0006g0165 |
3 | HG01884.hp2 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.478-2308_478-2301d others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | AACACACA others(3): Show |
A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0028 |
3 | HG01515.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.478-2310_478-2301d others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | AACACACA others(5): Show |
A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0029 others(1): Show |
10 | HG00099.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-2312_478-2301d others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | AACACACA others(7): Show |
A | 19 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0012 others(16): Show |
31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.478-2314_478-2301d others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742447 | AACACACA others(11): Show |
A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0048 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.478-2318_478-2301d others(20): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | |||||||
| chr16:46742493 | G | A | 1 | a0002c0002t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478-2346C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742493 | |||||||
| chr16:46742814 | C | G | 2 | a0001c0001t0001g0089 a0001c0007t0001g0051 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.478-2667G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742814 | |||||||
| chr16:46742837 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.478-2690T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742837 | |||||||
| chr16:46742884 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.478-2737A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742884 | |||||||
| chr16:46743149 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.478-3002C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743149 | |||||||
| chr16:46743151 | C | T | 25 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-3004G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743151 | |||||||
| chr16:46743168 | G | A | 1 | a0002c0002t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478-3021C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743168 | |||||||
| chr16:46743252 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-3105A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743252 | |||||||
| chr16:46743370 | A | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.478-3223T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743370 | |||||||
| chr16:46743405 | G | T | 25 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(22): Show |
44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-3258C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743405 | |||||||
| chr16:46743501 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478-3354A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743501 | |||||||
| chr16:46743501 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.478-3354A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743501 | |||||||
| chr16:46743541 | C | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.478-3394G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743541 | |||||||
| chr16:46743564 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.478-3417G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743564 | |||||||
| chr16:46743589 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.478-3442T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743589 | |||||||
| chr16:46743772 | C | T | 1 | a0002c0002t0001g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478-3625G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743772 | |||||||
| chr16:46744158 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(37): Show |
46 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.477+3559C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744158 | |||||||
| chr16:46744159 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.477+3558C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744159 | |||||||
| chr16:46744177 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.477+3540A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744177 | |||||||
| chr16:46744234 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.477+3483T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744234 | |||||||
| chr16:46744275 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.477+3442C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744275 | |||||||
| chr16:46744330 | C | CT | 27 | a0001c0001t0001g0159 a0001c0001t0001g0178 a0001c0001t0002g0001 others(24): Show |
44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.477+3386dupA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744330 | |||||||
| chr16:46744330 | C | CTT | 93 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(90): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.477+3385_477+3386d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744330 | |||||||
| chr16:46744330 | C | CTTT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(43): Show |
54 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.477+3384_477+3386d others(5): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744330 | |||||||
| chr16:46744364 | T | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(169): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.477+3353A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744364 | |||||||
| chr16:46744491 | G | A | 2 | a0001c0001t0001g0178 a0004c0004t0001g0016 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.477+3226C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744491 | |||||||
| chr16:46744769 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477+2948C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744769 | |||||||
| chr16:46744815 | T | C | 1 | a0002c0002t0001g0169 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.477+2902A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744815 | |||||||
| chr16:46745336 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.477+2381T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745336 | |||||||
| chr16:46745363 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.477+2354C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745363 | |||||||
| chr16:46745608 | T | C | 3 | a0002c0002t0001g0170 a0002c0002t0001g0171 a0002c0002t0001g0172 |
3 | HG00642.hp2 HG01069.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.477+2109A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745608 | |||||||
| chr16:46745837 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.477+1880C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745837 | |||||||
| chr16:46746056 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0011g0020 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.477+1661C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746056 | |||||||
| chr16:46746283 | A | G | 26 | a0001c0001t0001g0027 a0001c0001t0002g0001 a0001c0001t0002g0004 others(23): Show |
45 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.477+1434T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746283 | |||||||
| chr16:46746355 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01433.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+1362C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746355 | |||||||
| chr16:46746393 | A | G | 2 | a0001c0001t0001g0023 a0007c0005t0001g0022 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.477+1324T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746393 | |||||||
| chr16:46746398 | G | A | 1 | a0001c0001t0017g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+1319C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746398 | |||||||
| chr16:46746613 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0011g0020 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.477+1104G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746613 | |||||||
| chr16:46747100 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.477+617G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46747100 | |||||||
| chr16:46747218 | C | G | 1 | a0001c0001t0003g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.477+499G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46747218 |