Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79730 |
| ensemblid | ENSG00000179299.17 |
| hgncid | 25857 |
| symbol | NSUN7 |
| name | NOP2/Sun RNA methyltransferase family member 7 |
| refseq_nuc | NM_024677.6 |
| refseq_prot | NP_078953.4 |
| ensembl_nuc | ENST00000381782.7 |
| ensembl_prot | ENSP00000371201.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 40749955 |
| end | 40811184 |
| strand | + |
| ver | v1.2 |
| region | chr4:40749955-40811184 |
| region5000 | chr4:40744955-40816184 |
| regionname0 | NSUN7_chr4_40749955_40811184 |
| regionname5000 | NSUN7_chr4_40744955_40816184 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 718 | 212 | 48 | 45 | 96 | 6 | 16 | 80 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0002 | 0/0 | 718 | 100 | 12 | 5 | 67 | 0 | 16 | 53 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0003 | 0/0 | 718 | 50 | 13 | 24 | 6 | 2 | 5 | 5 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0004 | 0/0 | 718 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0005 | 1/0 | 718 | 3 | 0 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0006 | 0/0 | 718 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0007 | 0/0 | 718 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0008 | 0/0 | 718 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0009 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0010 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0011 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0012 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0013 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0014 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(523): Show |
chr4 | 40744955 | 40816184 |
| a0015 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0016 | 0/0 | 218 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(213): Show |
chr4 | 40744955 | 40816184 |
| a0017 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0018 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| a0019 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | MLNST others(713): Show |
chr4 | 40744955 | 40816184 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2154 | 211 | 47 | 45 | 96 | 6 | 16 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0001c0013 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0002c0002 | 0/0 | 2154 | 99 | 12 | 4 | 67 | 0 | 16 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0002c0010 | 0/0 | 2154 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0003c0003 | 0/0 | 2154 | 49 | 13 | 24 | 6 | 2 | 4 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0003c0022 | 0/0 | 2154 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0004c0004 | 0/0 | 2154 | 7 | 7 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0004c0014 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0005c0005 | 1/0 | 2154 | 3 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0006c0007 | 0/0 | 2154 | 3 | 1 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0007c0006 | 0/0 | 2154 | 3 | 2 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0008c0008 | 0/0 | 2154 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0009c0017 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0010c0018 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0011c0021 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0012c0023 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0013c0009 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0014c0012 | 0/0 | 2156 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2151): Show |
chr4 | 40744955 | 40816184 | ||
| a0015c0015 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0016c0019 | 0/0 | 2144 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2139): Show |
chr4 | 40744955 | 40816184 | ||
| a0017c0011 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0018c0016 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 | ||
| a0019c0020 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | ATGCT others(2149): Show |
chr4 | 40744955 | 40816184 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4839 | 116 | 25 | 22 | 61 | 1 | 6 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0002 | 0/0 | 4838 | 41 | 6 | 11 | 19 | 3 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0004 | 0/0 | 4840 | 10 | 2 | 3 | 4 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0005 | 0/0 | 4840 | 5 | 0 | 2 | 2 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0007 | 0/0 | 4840 | 6 | 1 | 0 | 5 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0009 | 0/0 | 4842 | 6 | 1 | 3 | 0 | 2 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4837): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0010 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4832): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0012 | 0/0 | 4841 | 3 | 2 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0013 | 0/0 | 4839 | 3 | 0 | 1 | 0 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0014 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0017 | 0/0 | 4843 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4838): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0018 | 0/0 | 4838 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0019 | 0/0 | 4838 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0020 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4837): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0027 | 0/0 | 4841 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0029 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0033 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0036 | 0/0 | 4838 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0037 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0038 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0039 | 0/0 | 4838 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0041 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0042 | 0/0 | 4839 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0043 | 0/0 | 4838 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0045 | 0/0 | 4844 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4839): Show |
chr4 | 40744955 | 40816184 |
| a0001c0001t0047 | 0/0 | 4843 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4838): Show |
chr4 | 40744955 | 40816184 |
| a0001c0013t0002 | 0/0 | 4838 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0001 | 0/0 | 4839 | 69 | 2 | 2 | 52 | 0 | 13 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0002 | 0/0 | 4838 | 5 | 4 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0004 | 0/0 | 4840 | 10 | 0 | 0 | 8 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0005 | 0/0 | 4840 | 6 | 0 | 1 | 4 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0010 | 0/0 | 4837 | 5 | 5 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4832): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0014 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0024 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0026 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0002c0002t0035 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0002c0010t0001 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0003 | 0/0 | 4843 | 25 | 1 | 17 | 1 | 2 | 4 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4838): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0006 | 0/0 | 4844 | 8 | 2 | 4 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4839): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0011 | 0/0 | 4840 | 4 | 3 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0014 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0015 | 0/0 | 4841 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0016 | 0/0 | 4841 | 3 | 3 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0021 | 0/0 | 4845 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4840): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0022 | 0/0 | 4844 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4839): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0025 | 0/0 | 4841 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0031 | 0/0 | 4843 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4838): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0032 | 0/0 | 4842 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4837): Show |
chr4 | 40744955 | 40816184 |
| a0003c0003t0044 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0003c0022t0003 | 0/0 | 4843 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4838): Show |
chr4 | 40744955 | 40816184 |
| a0004c0004t0008 | 0/0 | 4841 | 6 | 6 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0004c0004t0046 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4837): Show |
chr4 | 40744955 | 40816184 |
| a0004c0014t0008 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0005c0005t0001 | 1/0 | 4839 | 3 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0006c0007t0028 | 0/0 | 4840 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0006c0007t0030 | 0/0 | 4845 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4840): Show |
chr4 | 40744955 | 40816184 |
| a0006c0007t0048 | 0/0 | 4845 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4840): Show |
chr4 | 40744955 | 40816184 |
| a0007c0006t0003 | 0/0 | 4843 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4838): Show |
chr4 | 40744955 | 40816184 |
| a0007c0006t0015 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0007c0006t0034 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0008c0008t0001 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0008c0008t0005 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0009c0017t0023 | 0/0 | 4841 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0010c0018t0001 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0011c0021t0002 | 0/0 | 4838 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0012c0023t0001 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| a0013c0009t0007 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0014c0012t0001 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4836): Show |
chr4 | 40744955 | 40816184 |
| a0015c0015t0040 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4837): Show |
chr4 | 40744955 | 40816184 |
| a0016c0019t0002 | 0/0 | 4828 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4823): Show |
chr4 | 40744955 | 40816184 |
| a0017c0011t0004 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4835): Show |
chr4 | 40744955 | 40816184 |
| a0018c0016t0002 | 0/0 | 4838 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4833): Show |
chr4 | 40744955 | 40816184 |
| a0019c0020t0001 | 0/0 | 4839 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | AGTCG others(4834): Show |
chr4 | 40744955 | 40816184 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0009g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0009g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0009g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0009g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0009g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0012g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0012g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0013g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0013g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0013g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0014g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0017g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0017g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0018g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0018g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0019g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0020g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0027g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0029g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0033g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0036g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0037g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0038g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0039g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0041g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0042g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0043g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0045g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0001t0047g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0001c0013t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0001 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0005g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0014g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0024g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0026g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0002t0035g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0002c0010t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0011g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0014g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0016g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0016g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0016g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0021g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0022g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0025g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0032g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0003t0044g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0003c0022t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0004t0046g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0004c0014t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0005c0005t0001g0001 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0005c0005t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0005c0005t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0006c0007t0028g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0006c0007t0030g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0006c0007t0048g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0007c0006t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0007c0006t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0007c0006t0034g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0008c0008t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0008c0008t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0009c0017t0023g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0010c0018t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0011c0021t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0012c0023t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0013c0009t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0014c0012t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0015c0015t0040g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0016c0019t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0017c0011t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0018c0016t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| a0019c0020t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0003 | g0226 | EUR | GBR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | GBR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0292 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00438 | hp1 | a0003 | c0003 | t0022 | g0042 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00438 | hp2 | a0002 | c0002 | t0005 | g0286 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00597 | hp2 | a0009 | c0017 | t0023 | g0119 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00639 | hp2 | a0005 | c0005 | t0001 | g0280 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00642 | hp2 | a0003 | c0003 | t0006 | g0049 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00733 | hp2 | a0003 | c0003 | t0003 | g0030 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00735 | hp1 | a0003 | c0003 | t0003 | g0034 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0331 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG00738 | hp2 | a0003 | c0003 | t0003 | g0228 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01069 | hp1 | a0003 | c0003 | t0003 | g0033 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01069 | hp2 | a0003 | c0003 | t0006 | g0060 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01071 | hp1 | a0003 | c0003 | t0003 | g0032 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01074 | hp1 | a0003 | c0003 | t0003 | g0263 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01081 | hp1 | a0003 | c0003 | t0003 | g0040 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01081 | hp2 | a0003 | c0003 | t0003 | g0344 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01099 | hp1 | a0003 | c0003 | t0003 | g0044 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01106 | hp1 | a0003 | c0003 | t0003 | g0036 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01109 | hp2 | a0003 | c0003 | t0006 | g0059 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01167 | hp2 | a0003 | c0003 | t0025 | g0161 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01168 | hp2 | a0003 | c0003 | t0003 | g0028 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01169 | hp2 | a0003 | c0003 | t0011 | g0162 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01175 | hp2 | a0003 | c0003 | t0003 | g0343 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01192 | hp1 | a0001 | c0001 | t0036 | g0209 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01192 | hp2 | a0001 | c0001 | t0017 | g0180 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01243 | hp1 | a0006 | c0007 | t0028 | g0043 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01243 | hp2 | a0005 | c0005 | t0001 | g0291 | AMR | PUR | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01255 | hp1 | a0003 | c0003 | t0003 | g0345 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01255 | hp2 | a0003 | c0003 | t0003 | g0237 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01258 | hp1 | a0002 | c0010 | t0001 | g0051 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01261 | hp2 | a0003 | c0003 | t0003 | g0231 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01358 | hp1 | a0006 | c0007 | t0048 | g0236 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01361 | hp1 | a0003 | c0003 | t0032 | g0039 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0334 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01496 | hp2 | a0003 | c0003 | t0003 | g0340 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01516 | hp2 | a0001 | c0001 | t0009 | g0329 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0328 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01517 | hp2 | a0003 | c0003 | t0003 | g0029 | EUR | IBS | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01891 | hp1 | a0002 | c0002 | t0024 | g0171 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01928 | hp2 | a0001 | c0001 | t0038 | g0178 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01975 | hp1 | a0002 | c0002 | t0026 | g0065 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01978 | hp1 | a0002 | c0002 | t0005 | g0304 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01981 | hp1 | a0003 | c0003 | t0003 | g0035 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0332 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0336 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02055 | hp2 | a0006 | c0007 | t0030 | g0045 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02071 | hp2 | a0010 | c0018 | t0001 | g0357 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02080 | hp2 | a0011 | c0021 | t0002 | g0084 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02129 | hp2 | a0012 | c0023 | t0001 | g0007 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0324 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02258 | hp1 | a0001 | c0001 | t0019 | g0224 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02280 | hp1 | a0013 | c0009 | t0007 | g0325 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02280 | hp2 | a0004 | c0004 | t0046 | g0067 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02300 | hp1 | a0003 | c0003 | t0006 | g0061 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02523 | hp1 | a0008 | c0008 | t0001 | g0062 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02602 | hp1 | a0002 | c0002 | t0005 | g0005 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02602 | hp2 | a0001 | c0001 | t0042 | g0232 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02622 | hp1 | a0001 | c0001 | t0045 | g0066 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02630 | hp2 | a0004 | c0004 | t0008 | g0070 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02698 | hp1 | a0003 | c0003 | t0003 | g0214 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02698 | hp2 | a0001 | c0001 | t0043 | g0091 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02717 | hp2 | a0002 | c0002 | t0010 | g0136 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02723 | hp2 | a0001 | c0001 | t0037 | g0156 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02809 | hp2 | a0001 | c0001 | t0019 | g0223 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02818 | hp1 | a0003 | c0003 | t0011 | g0163 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02895 | hp2 | a0002 | c0002 | t0010 | g0097 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02922 | hp2 | a0003 | c0003 | t0044 | g0160 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02965 | hp1 | a0003 | c0003 | t0016 | g0348 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02965 | hp2 | a0004 | c0004 | t0008 | g0069 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02970 | hp2 | a0001 | c0013 | t0002 | g0153 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02976 | hp1 | a0004 | c0004 | t0008 | g0068 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02976 | hp2 | a0001 | c0001 | t0039 | g0230 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0175 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03041 | hp2 | a0003 | c0003 | t0015 | g0240 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03098 | hp2 | a0004 | c0004 | t0008 | g0072 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03130 | hp1 | a0014 | c0012 | t0001 | g0014 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03130 | hp2 | a0004 | c0004 | t0008 | g0071 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03139 | hp1 | a0004 | c0004 | t0008 | g0073 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03139 | hp2 | a0001 | c0001 | t0033 | g0082 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03195 | hp2 | a0004 | c0014 | t0008 | g0046 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03209 | hp1 | a0015 | c0015 | t0040 | g0174 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0306 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0038 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03239 | hp2 | a0003 | c0003 | t0003 | g0333 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03453 | hp1 | a0003 | c0003 | t0011 | g0159 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03453 | hp2 | a0002 | c0002 | t0010 | g0166 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03486 | hp1 | a0003 | c0003 | t0016 | g0354 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03491 | hp1 | a0003 | c0003 | t0003 | g0341 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03491 | hp2 | a0002 | c0002 | t0004 | g0020 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0020 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03516 | hp1 | a0003 | c0003 | t0031 | g0031 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03516 | hp2 | a0003 | c0003 | t0011 | g0177 | AFR | ESN | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03579 | hp1 | a0003 | c0003 | t0015 | g0158 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03579 | hp2 | a0001 | c0001 | t0047 | g0074 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03654 | hp2 | a0003 | c0022 | t0003 | g0346 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0052 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0298 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03704 | hp1 | a0001 | c0001 | t0013 | g0339 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0296 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0321 | SAS | PJL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0337 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03834 | hp2 | a0001 | c0001 | t0027 | g0335 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04115 | hp1 | a0007 | c0006 | t0003 | g0302 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | BEB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04199 | hp1 | a0001 | c0001 | t0013 | g0327 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | STU | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0323 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18906 | hp1 | a0007 | c0006 | t0034 | g0356 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18947 | hp1 | a0002 | c0002 | t0005 | g0316 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18947 | hp2 | a0003 | c0003 | t0021 | g0037 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18948 | hp2 | a0016 | c0019 | t0002 | g0105 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18956 | hp2 | a0002 | c0002 | t0004 | g0301 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18965 | hp2 | a0002 | c0002 | t0004 | g0318 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18967 | hp2 | a0002 | c0002 | t0004 | g0271 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18969 | hp2 | a0001 | c0001 | t0007 | g0245 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18970 | hp1 | a0003 | c0003 | t0006 | g0362 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18973 | hp2 | a0003 | c0003 | t0006 | g0361 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18979 | hp1 | a0002 | c0002 | t0004 | g0326 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18983 | hp2 | a0001 | c0001 | t0018 | g0025 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18984 | hp2 | a0017 | c0011 | t0004 | g0358 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18985 | hp2 | a0001 | c0001 | t0041 | g0248 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18987 | hp2 | a0002 | c0002 | t0004 | g0322 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18989 | hp1 | a0002 | c0002 | t0005 | g0359 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18990 | hp2 | a0001 | c0001 | t0029 | g0250 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18999 | hp2 | a0003 | c0003 | t0014 | g0167 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19003 | hp2 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0246 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19004 | hp2 | a0002 | c0002 | t0004 | g0261 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19056 | hp1 | a0002 | c0002 | t0004 | g0274 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19056 | hp2 | a0018 | c0016 | t0002 | g0185 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0360 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19067 | hp2 | a0002 | c0002 | t0005 | g0170 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19077 | hp1 | a0001 | c0001 | t0014 | g0132 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19077 | hp2 | a0002 | c0002 | t0014 | g0307 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19079 | hp1 | a0002 | c0002 | t0035 | g0350 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19079 | hp2 | a0008 | c0008 | t0005 | g0022 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19090 | hp2 | a0001 | c0001 | t0018 | g0026 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0242 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0355 | AFR | YRI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0217 | AFR | ASW | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ASW | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | TSI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0279 | SAS | GIH | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0278 | SAS | GIH | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0338 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0305 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02486 | hp1 | a0002 | c0002 | t0010 | g0120 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02559 | hp1 | a0007 | c0006 | t0015 | g0168 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG02559 | hp2 | a0003 | c0003 | t0006 | g0165 | AFR | ACB | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03471 | hp1 | a0003 | c0003 | t0006 | g0363 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| HG06807 | hp2 | a0003 | c0003 | t0016 | g0239 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20300 | hp1 | a0002 | c0002 | t0010 | g0145 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0225 | AFR | USA | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | LWK | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| NA21309 | hp2 | a0019 | c0020 | t0001 | g0313 | AFR | LWK | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| homoSapiens | grch38p0 | a0005 | c0005 | t0001 | g0001 | REF | REF | NSUN7_chr4_40744955_40816184 | NSUN7 | chr4 | 40744955 | 40816184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:40750709 | G | T | 1 | a0012 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.16G>T | p.Gly6Cys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 453/4839 | 16/2157 | 6/718 | chr4 | 40750709 | |||
| chr4:40750718 | G | A | 1 | a0013 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.25G>A | p.Glu9Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 462/4839 | 25/2157 | 9/718 | chr4 | 40750718 | |||
| chr4:40761226 | A | T | 1 | a0011 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.413A>T | p.Lys138Ile | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/12 | 850/4839 | 413/2157 | 138/718 | chr4 | 40761226 | |||
| chr4:40774312 | A | G | 1 | a0019 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.536A>G | p.His179Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/12 | 973/4839 | 536/2157 | 179/718 | chr4 | 40774312 | |||
| chr4:40774777 | GTTTATAA others(3): Show |
G | 1 | a0016 | 1 | NA18948.hp2 | frameshift_variant | HIGH | c.656_665delATAATAAT others(2): Show |
p.Tyr219fs | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/12 | 1093/4839 | 656/2157 | 219/718 | INFO_REALIGN_3_PRIME | chr4 | 40774777 | ||
| chr4:40776086 | C | T | 1 | a0010 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.863C>T | p.Ala288Val | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1300/4839 | 863/2157 | 288/718 | chr4 | 40776086 | |||
| chr4:40776145 | T | G | 13 | a0001 a0003 a0004 others(10): Show |
282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
missense_variant | MODERATE | c.922T>G | p.Ser308Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1359/4839 | 922/2157 | 308/718 | chr4 | 40776145 | |||
| chr4:40776239 | T | C | 1 | a0008 | 2 | HG02523.hp1 NA19079.hp2 |
missense_variant | MODERATE | c.1016T>C | p.Phe339Ser | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1453/4839 | 1016/2157 | 339/718 | chr4 | 40776239 | |||
| chr4:40790689 | G | A | 1 | a0006 | 3 | HG01243.hp1 HG01358.hp1 HG02055.hp2 |
missense_variant | MODERATE | c.1124G>A | p.Arg375His | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/12 | 1561/4839 | 1124/2157 | 375/718 | chr4 | 40790689 | |||
| chr4:40794465 | A | G | 1 | a0009 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1271A>G | p.His424Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/12 | 1708/4839 | 1271/2157 | 424/718 | chr4 | 40794465 | |||
| chr4:40808334 | A | T | 1 | a0018 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.1552A>T | p.Asn518Tyr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1989/4839 | 1552/2157 | 518/718 | chr4 | 40808334 | |||
| chr4:40808355 | G | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1573G>A | p.Ala525Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2010/4839 | 1573/2157 | 525/718 | chr4 | 40808355 | |||
| chr4:40808358 | GCCAAGGG others(6): Show |
G | 1 | a0014 | 1 | HG03130.hp1 | frameshift_variant | HIGH | c.1577_1589delCCAAGG others(7): Show |
p.Ala526fs | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2014/4839 | 1577/2157 | 526/718 | chr4 | 40808358 | |||
| chr4:40808375 | T | G | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1593T>G | p.Asp531Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2030/4839 | 1593/2157 | 531/718 | chr4 | 40808375 | |||
| chr4:40808376 | G | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1594G>A | p.Gly532Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2031/4839 | 1594/2157 | 532/718 | chr4 | 40808376 | |||
| chr4:40808382 | G | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1600G>A | p.Glu534Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2037/4839 | 1600/2157 | 534/718 | chr4 | 40808382 | |||
| chr4:40808385 | T | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1603T>A | p.Leu535Met | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2040/4839 | 1603/2157 | 535/718 | chr4 | 40808385 | |||
| chr4:40808386 | T | A | 1 | a0014 | 1 | HG03130.hp1 | stop_gained | HIGH | c.1604T>A | p.Leu535* | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2041/4839 | 1604/2157 | 535/718 | chr4 | 40808386 | |||
| chr4:40808388 | G | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1606G>A | p.Gly536Ser | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2043/4839 | 1606/2157 | 536/718 | chr4 | 40808388 | |||
| chr4:40808389 | G | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1607G>A | p.Gly536Asp | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2044/4839 | 1607/2157 | 536/718 | chr4 | 40808389 | |||
| chr4:40808394 | T | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1612T>A | p.Ser538Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2049/4839 | 1612/2157 | 538/718 | chr4 | 40808394 | |||
| chr4:40808395 | C | A | 1 | a0014 | 1 | HG03130.hp1 | stop_gained | HIGH | c.1613C>A | p.Ser538* | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2050/4839 | 1613/2157 | 538/718 | chr4 | 40808395 | |||
| chr4:40808397 | T | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1615T>A | p.Ser539Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2052/4839 | 1615/2157 | 539/718 | chr4 | 40808397 | |||
| chr4:40808398 | C | A | 1 | a0014 | 1 | HG03130.hp1 | stop_gained | HIGH | c.1616C>A | p.Ser539* | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2053/4839 | 1616/2157 | 539/718 | chr4 | 40808398 | |||
| chr4:40808406 | G | A | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1624G>A | p.Glu542Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2061/4839 | 1624/2157 | 542/718 | chr4 | 40808406 | |||
| chr4:40808418 | A | AAATCAGT others(8): Show |
1 | a0014 | 1 | HG03130.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.1638_1639insTCAGTG others(9): Show |
p.Lys546_Lys547insSe others(13): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2076/4839 | 1639/2157 | 547/718 | INFO_REALIGN_3_PRIME | chr4 | 40808418 | ||
| chr4:40808472 | A | C | 1 | a0015 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1690A>C | p.Met564Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2127/4839 | 1690/2157 | 564/718 | chr4 | 40808472 | |||
| chr4:40808646 | A | G | 3 | a0003 a0006 a0007 |
56 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(53): Show |
missense_variant | MODERATE | c.1864A>G | p.Thr622Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2301/4839 | 1864/2157 | 622/718 | chr4 | 40808646 | |||
| chr4:40808730 | A | G | 18 | a0001 a0002 a0003 others(15): Show |
388 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(385): Show |
missense_variant | MODERATE | c.1948A>G | p.Lys650Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2385/4839 | 1948/2157 | 650/718 | chr4 | 40808730 | |||
| chr4:40808839 | T | G | 1 | a0004 | 8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
missense_variant | MODERATE | c.2057T>G | p.Val686Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2494/4839 | 2057/2157 | 686/718 | chr4 | 40808839 | |||
| chr4:40808887 | C | T | 1 | a0017 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.2105C>T | p.Pro702Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2542/4839 | 2105/2157 | 702/718 | chr4 | 40808887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:40750813 | G | C | 1 | a0002c0010 | 1 | HG01258.hp1 | synonymous_variant | LOW | c.120G>C | p.Thr40Thr | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 557/4839 | 120/2157 | 40/718 | chr4 | 40750813 | |||
| chr4:40750924 | C | G | 1 | a0003c0022 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.231C>G | p.Ser77Ser | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 668/4839 | 231/2157 | 77/718 | chr4 | 40750924 | |||
| chr4:40776129 | C | T | 16 | a0001c0001 a0001c0013 a0003c0003 others(13): Show |
282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
synonymous_variant | LOW | c.906C>T | p.Gly302Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/12 | 1343/4839 | 906/2157 | 302/718 | chr4 | 40776129 | |||
| chr4:40808354 | T | G | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1572T>G | p.Ala524Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2009/4839 | 1572/2157 | 524/718 | chr4 | 40808354 | |||
| chr4:40808372 | G | T | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1590G>T | p.Leu530Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2027/4839 | 1590/2157 | 530/718 | chr4 | 40808372 | |||
| chr4:40808378 | G | T | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1596G>T | p.Gly532Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2033/4839 | 1596/2157 | 532/718 | chr4 | 40808378 | |||
| chr4:40808381 | T | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1599T>A | p.Ile533Ile | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2036/4839 | 1599/2157 | 533/718 | chr4 | 40808381 | |||
| chr4:40808384 | G | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1602G>A | p.Glu534Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2039/4839 | 1602/2157 | 534/718 | chr4 | 40808384 | |||
| chr4:40808387 | G | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1605G>A | p.Leu535Leu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2042/4839 | 1605/2157 | 535/718 | chr4 | 40808387 | |||
| chr4:40808390 | T | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1608T>A | p.Gly536Gly | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2045/4839 | 1608/2157 | 536/718 | chr4 | 40808390 | |||
| chr4:40808403 | C | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1621C>A | p.Arg541Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2058/4839 | 1621/2157 | 541/718 | chr4 | 40808403 | |||
| chr4:40808405 | G | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1623G>A | p.Arg541Arg | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2060/4839 | 1623/2157 | 541/718 | chr4 | 40808405 | |||
| chr4:40808408 | G | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1626G>A | p.Glu542Glu | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2063/4839 | 1626/2157 | 542/718 | chr4 | 40808408 | |||
| chr4:40808411 | G | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1629G>A | p.Lys543Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2066/4839 | 1629/2157 | 543/718 | chr4 | 40808411 | |||
| chr4:40808417 | G | A | 1 | a0014c0012 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1635G>A | p.Lys545Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2072/4839 | 1635/2157 | 545/718 | chr4 | 40808417 | |||
| chr4:40808606 | G | A | 1 | a0001c0013 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1824G>A | p.Lys608Lys | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2261/4839 | 1824/2157 | 608/718 | chr4 | 40808606 | |||
| chr4:40808717 | T | C | 1 | a0004c0014 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1935T>C | p.Ala645Ala | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2372/4839 | 1935/2157 | 645/718 | chr4 | 40808717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:40750042 | C | T | 1 | a0001c0001t0019 | 2 | HG02258.hp1 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-350C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 652 | chr4 | 40750042 | ||||||
| chr4:40750081 | C | T | 2 | a0003c0003t0016 a0006c0007t0048 |
4 | HG01358.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-311C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 613 | chr4 | 40750081 | ||||||
| chr4:40750105 | C | T | 5 | a0001c0001t0045 a0001c0001t0047 a0004c0004t0008 others(2): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-287C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 589 | chr4 | 40750105 | ||||||
| chr4:40750136 | A | AC | 11 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0020 others(8): Show |
21 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-250dupC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 551 | INFO_REALIGN_3_PRIME | chr4 | 40750136 | |||||
| chr4:40750233 | A | G | 1 | a0003c0003t0044 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/12 | 461 | chr4 | 40750233 | ||||||
| chr4:40750687 | G | A | 1 | a0002c0002t0026 | 1 | HG01975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/12 | 7 | chr4 | 40750687 | ||||||
| chr4:40808961 | G | A | 6 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0013 others(3): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*22G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 22 | chr4 | 40808961 | ||||||
| chr4:40809193 | G | C | 1 | a0006c0007t0028 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 254 | chr4 | 40809193 | ||||||
| chr4:40809196 | C | T | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG02602.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*257C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 257 | chr4 | 40809196 | ||||||
| chr4:40809216 | T | G | 1 | a0001c0001t0029 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 277 | chr4 | 40809216 | ||||||
| chr4:40809259 | G | A | 3 | a0004c0004t0008 a0004c0004t0046 a0004c0014t0008 |
8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*320G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 320 | chr4 | 40809259 | ||||||
| chr4:40809389 | C | T | 3 | a0001c0001t0007 a0001c0001t0041 a0013c0009t0007 |
8 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 450 | chr4 | 40809389 | ||||||
| chr4:40809664 | A | G | 13 | a0001c0001t0045 a0001c0001t0047 a0003c0003t0011 others(10): Show |
24 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*725A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 725 | chr4 | 40809664 | ||||||
| chr4:40809726 | A | AATT | 10 | a0003c0003t0003 a0003c0003t0006 a0003c0003t0021 others(7): Show |
41 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*790dupATT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 791 | INFO_REALIGN_3_PRIME | chr4 | 40809726 | |||||
| chr4:40809832 | A | G | 1 | a0001c0001t0039 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 893 | chr4 | 40809832 | ||||||
| chr4:40809902 | A | C | 1 | a0001c0001t0038 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 963 | chr4 | 40809902 | ||||||
| chr4:40809936 | A | T | 3 | a0001c0001t0007 a0001c0001t0041 a0013c0009t0007 |
8 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*997A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 997 | chr4 | 40809936 | ||||||
| chr4:40810154 | C | T | 1 | a0001c0001t0027 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1215C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1215 | chr4 | 40810154 | ||||||
| chr4:40810348 | C | T | 1 | a0006c0007t0028 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1409C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1409 | chr4 | 40810348 | ||||||
| chr4:40810357 | C | T | 1 | a0001c0001t0037 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1418 | chr4 | 40810357 | ||||||
| chr4:40810494 | CTT | C | 3 | a0004c0004t0008 a0004c0004t0046 a0004c0014t0008 |
8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1556_*1557delTT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1556 | chr4 | 40810494 | ||||||
| chr4:40810577 | C | CA | 19 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0045 others(16): Show |
74 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1662dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1663 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | |||||
| chr4:40810577 | C | CAA | 13 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0020 others(10): Show |
25 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1661_*1662dupAA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1663 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | |||||
| chr4:40810577 | C | CAAA | 4 | a0001c0001t0009 a0001c0001t0017 a0006c0007t0030 others(1): Show |
10 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1660_*1662dupAAA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1663 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | |||||
| chr4:40810577 | CA | C | 12 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0019 others(9): Show |
58 | HG00140.hp2 HG00621.hp2 HG00738.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1662delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1662 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | |||||
| chr4:40810577 | CAA | C | 2 | a0001c0001t0010 a0002c0002t0010 |
6 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1661_*1662delAA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1661 | INFO_REALIGN_3_PRIME | chr4 | 40810577 | |||||
| chr4:40810619 | A | C | 1 | a0002c0002t0035 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1680 | chr4 | 40810619 | ||||||
| chr4:40810652 | T | C | 23 | a0001c0001t0045 a0001c0001t0047 a0003c0003t0003 others(20): Show |
65 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1713T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1713 | chr4 | 40810652 | ||||||
| chr4:40810705 | A | G | 1 | a0007c0006t0034 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1766 | chr4 | 40810705 | ||||||
| chr4:40810723 | T | G | 1 | a0001c0001t0018 | 2 | NA18983.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1784T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1784 | chr4 | 40810723 | ||||||
| chr4:40810849 | G | A | 1 | a0003c0003t0031 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1910G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1910 | chr4 | 40810849 | ||||||
| chr4:40810892 | G | C | 1 | a0001c0001t0033 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1953G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1953 | chr4 | 40810892 | ||||||
| chr4:40810933 | A | G | 1 | a0001c0001t0036 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1994A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 1994 | chr4 | 40810933 | ||||||
| chr4:40811100 | T | TATC | 6 | a0001c0001t0045 a0001c0001t0047 a0004c0004t0008 others(3): Show |
11 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2162_*2164dupATC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 12/12 | 2165 | INFO_REALIGN_3_PRIME | chr4 | 40811100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:40750367 | T | C | 1 | a0008c0008t0005g0022 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-92+67T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | chr4 | 40750367 | |||||||
| chr4:40750444 | C | CT | 15 | a0001c0001t0002g0353 a0002c0002t0001g0349 a0002c0002t0001g0351 others(12): Show |
15 | HG02071.hp2 HG03471.hp1 HG03486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-91-143dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 40750444 | ||||||
| chr4:40750444 | CT | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(142): Show |
153 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(150): Show |
intron_variant | MODIFIER | c.-91-143delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 40750444 | ||||||
| chr4:40750444 | CTT | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(23): Show |
27 | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.-91-144_-91-143del others(2): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 40750444 | ||||||
| chr4:40751079 | T | G | 1 | a0004c0014t0008g0046 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.298+88T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751079 | |||||||
| chr4:40751085 | A | G | 1 | a0003c0003t0006g0363 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.298+94A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751085 | |||||||
| chr4:40751138 | A | G | 1 | a0003c0003t0016g0348 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+147A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751138 | |||||||
| chr4:40751155 | A | T | 1 | a0001c0001t0002g0347 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.298+164A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751155 | |||||||
| chr4:40751232 | G | T | 1 | a0003c0022t0003g0346 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298+241G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751232 | |||||||
| chr4:40751289 | T | C | 4 | a0002c0002t0001g0349 a0002c0002t0001g0351 a0002c0002t0001g0352 others(1): Show |
4 | NA18968.hp1 NA19009.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+298T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751289 | |||||||
| chr4:40751380 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298+389C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751380 | |||||||
| chr4:40751421 | GC | G | 6 | a0001c0001t0002g0342 a0003c0003t0003g0340 a0003c0003t0003g0341 others(3): Show |
6 | HG01074.hp2 HG01081.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+432delC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40751421 | ||||||
| chr4:40751466 | G | A | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.298+475G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751466 | |||||||
| chr4:40751505 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
256 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.298+514G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751505 | |||||||
| chr4:40751549 | G | A | 24 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0048 others(21): Show |
24 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.298+558G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751549 | |||||||
| chr4:40751569 | A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.298+578A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751569 | |||||||
| chr4:40751610 | A | T | 1 | a0002c0002t0010g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.298+619A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751610 | |||||||
| chr4:40751754 | G | A | 65 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(62): Show |
66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.298+763G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751754 | |||||||
| chr4:40751763 | G | A | 3 | a0002c0002t0001g0355 a0007c0006t0015g0168 a0007c0006t0034g0356 |
3 | HG02559.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.298+772G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751763 | |||||||
| chr4:40751819 | C | T | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+828C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40751819 | |||||||
| chr4:40752011 | GACCAAAT others(10): Show |
G | 1 | a0001c0001t0001g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.298+1021_298+1037d others(19): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752011 | |||||||
| chr4:40752068 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0004g0008 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1077G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752068 | |||||||
| chr4:40752132 | A | G | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(65): Show |
69 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.298+1141A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752132 | |||||||
| chr4:40752137 | C | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.298+1146C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752137 | |||||||
| chr4:40752189 | C | CCTAAAGA others(3): Show |
1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1206_298+1207i others(12): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40752189 | ||||||
| chr4:40752200 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1209A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752200 | |||||||
| chr4:40752206 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1215A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752206 | |||||||
| chr4:40752230 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1239A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752230 | |||||||
| chr4:40752231 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1240T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752231 | |||||||
| chr4:40752235 | C | G | 1 | a0002c0002t0004g0326 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.298+1244C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752235 | |||||||
| chr4:40752260 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1269T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752260 | |||||||
| chr4:40752268 | C | T | 1 | a0008c0008t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.298+1277C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752268 | |||||||
| chr4:40752274 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1283A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752274 | |||||||
| chr4:40752275 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1284G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752275 | |||||||
| chr4:40752299 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1308A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752299 | |||||||
| chr4:40752300 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1309G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752300 | |||||||
| chr4:40752301 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1310A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752301 | |||||||
| chr4:40752303 | G | T | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1312G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752303 | |||||||
| chr4:40752307 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1316T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752307 | |||||||
| chr4:40752308 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1317G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752308 | |||||||
| chr4:40752309 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1318G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752309 | |||||||
| chr4:40752311 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1320T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752311 | |||||||
| chr4:40752312 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.298+1321T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752312 | |||||||
| chr4:40752334 | T | C | 4 | a0002c0002t0001g0253 a0002c0002t0001g0254 a0002c0002t0001g0355 others(1): Show |
4 | HG03834.hp1 HG04115.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1343T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752334 | |||||||
| chr4:40752339 | G | A | 1 | a0002c0002t0001g0255 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.298+1348G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752339 | |||||||
| chr4:40752485 | A | G | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(71): Show |
75 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.298+1494A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752485 | |||||||
| chr4:40752608 | G | A | 65 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(62): Show |
66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.298+1617G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752608 | |||||||
| chr4:40752609 | A | G | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+1618A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752609 | |||||||
| chr4:40752743 | A | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
8 | HG01891.hp2 HG02723.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+1752A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752743 | |||||||
| chr4:40752821 | A | ATAATGTA others(58): Show |
275 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(272): Show |
285 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.298+1830_298+1831i others(67): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752821 | |||||||
| chr4:40752821 | A | ATAATGTG others(58): Show |
1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+1830_298+1831i others(67): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752821 | |||||||
| chr4:40752822 | G | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(273): Show |
286 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.298+1831G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752822 | |||||||
| chr4:40752899 | C | G | 1 | a0001c0001t0047g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.298+1908C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40752899 | |||||||
| chr4:40753010 | C | T | 1 | a0002c0002t0004g0322 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.298+2019C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753010 | |||||||
| chr4:40753280 | CT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
30 | HG00408.hp1 HG01070.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.298+2304delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40753280 | ||||||
| chr4:40753309 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+2318C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753309 | |||||||
| chr4:40753388 | G | A | 1 | a0002c0002t0001g0257 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.298+2397G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753388 | |||||||
| chr4:40753488 | G | T | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+2497G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753488 | |||||||
| chr4:40753507 | G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+2516G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753507 | |||||||
| chr4:40753536 | G | C | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.298+2545G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753536 | |||||||
| chr4:40753695 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.298+2704G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753695 | |||||||
| chr4:40753718 | C | T | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+2727C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753718 | |||||||
| chr4:40753894 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+2903C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40753894 | |||||||
| chr4:40754042 | A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.298+3051A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754042 | |||||||
| chr4:40754134 | CCTG | C | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+3146_298+3148d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40754134 | ||||||
| chr4:40754146 | C | CT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
89 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.298+3170dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40754146 | ||||||
| chr4:40754216 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298+3225C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754216 | |||||||
| chr4:40754217 | G | A | 1 | a0001c0001t0038g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.298+3226G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754217 | |||||||
| chr4:40754319 | G | A | 1 | a0003c0003t0003g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.298+3328G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754319 | |||||||
| chr4:40754639 | G | A | 2 | a0001c0013t0002g0153 a0015c0015t0040g0174 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+3648G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754639 | |||||||
| chr4:40754694 | C | G | 4 | a0003c0003t0015g0240 a0003c0003t0016g0239 a0003c0003t0016g0348 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+3703C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754694 | |||||||
| chr4:40754738 | A | G | 3 | a0002c0002t0001g0319 a0002c0002t0001g0320 a0002c0002t0004g0318 |
3 | HG02129.hp1 NA18965.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.298+3747A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754738 | |||||||
| chr4:40754864 | CCTT | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG01346.hp2 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+3875_298+3877d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40754864 | ||||||
| chr4:40754881 | A | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(163): Show |
171 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.298+3890A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754881 | |||||||
| chr4:40754939 | C | A | 8 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(5): Show |
8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+3948C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754939 | |||||||
| chr4:40754952 | T | C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0330 a0001c0001t0002g0176 others(13): Show |
17 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.298+3961T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40754952 | |||||||
| chr4:40755016 | G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+4025G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755016 | |||||||
| chr4:40755143 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.298+4152G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755143 | |||||||
| chr4:40755151 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
78 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+4160G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755151 | |||||||
| chr4:40755203 | C | T | 3 | a0001c0013t0002g0153 a0003c0003t0006g0165 a0015c0015t0040g0174 |
3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+4212C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755203 | |||||||
| chr4:40755244 | C | T | 1 | a0001c0001t0004g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.298+4253C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755244 | |||||||
| chr4:40755250 | C | T | 1 | a0002c0002t0026g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.298+4259C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755250 | |||||||
| chr4:40755279 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.298+4288C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755279 | |||||||
| chr4:40755332 | C | T | 1 | a0003c0003t0015g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.298+4341C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755332 | |||||||
| chr4:40755418 | AT | A | 16 | a0001c0001t0001g0229 a0001c0001t0002g0186 a0001c0001t0002g0187 others(13): Show |
16 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.298+4436delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40755418 | ||||||
| chr4:40755491 | T | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+4500T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40755491 | |||||||
| chr4:40756062 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-4372C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756062 | |||||||
| chr4:40756109 | T | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
180 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.299-4325T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756109 | |||||||
| chr4:40756205 | C | T | 3 | a0001c0013t0002g0153 a0003c0003t0006g0165 a0015c0015t0040g0174 |
3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-4229C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756205 | |||||||
| chr4:40756211 | A | G | 3 | a0001c0013t0002g0153 a0003c0003t0006g0165 a0015c0015t0040g0174 |
3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-4223A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756211 | |||||||
| chr4:40756257 | C | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-4177C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756257 | |||||||
| chr4:40756289 | G | A | 1 | a0002c0002t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-4145G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756289 | |||||||
| chr4:40756380 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-4054C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756380 | |||||||
| chr4:40756398 | A | G | 1 | a0001c0001t0013g0339 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-4036A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756398 | |||||||
| chr4:40756499 | A | G | 1 | a0003c0003t0003g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.299-3935A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756499 | |||||||
| chr4:40756508 | A | G | 22 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(19): Show |
22 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-3926A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756508 | |||||||
| chr4:40756686 | A | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-3748A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756686 | |||||||
| chr4:40756741 | T | C | 1 | a0002c0002t0001g0355 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-3693T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40756741 | |||||||
| chr4:40756845 | AAAAGCT | A | 6 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-3587_299-3582d others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40756845 | ||||||
| chr4:40757178 | G | A | 1 | a0001c0001t0007g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.299-3256G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757178 | |||||||
| chr4:40757231 | TAAATAAA others(5): Show |
T | 1 | a0001c0001t0001g0013 | 2 | NA19083.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.299-3184_299-3173d others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757231 | ||||||
| chr4:40757298 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-3136G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757298 | |||||||
| chr4:40757493 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-2941A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757493 | |||||||
| chr4:40757535 | TTA | T | 3 | a0001c0001t0001g0259 a0003c0003t0006g0363 a0003c0003t0015g0240 |
3 | HG01099.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-2884_299-2883d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757535 | ||||||
| chr4:40757544 | TATATATA others(25): Show |
T | 8 | a0004c0004t0008g0068 a0004c0004t0008g0069 a0004c0004t0008g0070 others(5): Show |
8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-2882_299-2851d others(34): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757544 | ||||||
| chr4:40757552 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-2882A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757552 | |||||||
| chr4:40757556 | T | TTA | 3 | a0001c0013t0002g0153 a0003c0003t0006g0165 a0015c0015t0040g0174 |
3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-2865_299-2864d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757556 | ||||||
| chr4:40757579 | ATATATAT others(12): Show |
A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-2846_299-2828d others(21): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757579 | ||||||
| chr4:40757588 | C | CACATTGT others(12): Show |
1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-2825_299-2807d others(21): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757588 | ||||||
| chr4:40757588 | CACATTGT others(33): Show |
C | 1 | a0001c0001t0007g0245 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-2817_299-2778d others(42): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757588 | ||||||
| chr4:40757594 | GTGTGTAT others(50): Show |
G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299-2806_299-2750d others(59): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757594 | ||||||
| chr4:40757628 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
177 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.299-2806T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757628 | |||||||
| chr4:40757651 | T | TTGTGTGT others(35): Show |
1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-2778_299-2777i others(44): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757651 | ||||||
| chr4:40757657 | A | G | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-2777A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757657 | |||||||
| chr4:40757664 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-2770T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757664 | |||||||
| chr4:40757668 | T | C | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2766T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757668 | |||||||
| chr4:40757689 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-2745C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757689 | |||||||
| chr4:40757697 | A | T | 1 | a0007c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-2737A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757697 | |||||||
| chr4:40757725 | T | C | 2 | a0002c0002t0001g0257 a0002c0002t0001g0260 |
2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.299-2709T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757725 | |||||||
| chr4:40757725 | T | TATAC | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2708_299-2707i others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757725 | ||||||
| chr4:40757725 | TAC | T | 20 | a0001c0001t0001g0021 a0001c0001t0001g0330 a0001c0001t0002g0176 others(17): Show |
21 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-2685_299-2684d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757725 | ||||||
| chr4:40757725 | TACAC | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(238): Show |
250 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.299-2687_299-2684d others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757725 | ||||||
| chr4:40757727 | C | T | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-2707C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757727 | |||||||
| chr4:40757729 | C | T | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-2705C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757729 | |||||||
| chr4:40757731 | C | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
168 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.299-2703C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757731 | |||||||
| chr4:40757902 | T | G | 4 | a0001c0013t0002g0153 a0003c0003t0006g0165 a0015c0015t0040g0174 others(1): Show |
4 | HG02559.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-2532T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40757902 | |||||||
| chr4:40757902 | T | TTTTG | 33 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0139 others(30): Show |
34 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.299-2504_299-2501d others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757902 | ||||||
| chr4:40757902 | T | TTTTGTTT others(1): Show |
203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(200): Show |
212 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.299-2508_299-2501d others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757902 | ||||||
| chr4:40757902 | T | TTTTGTTT others(5): Show |
27 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0179 others(24): Show |
27 | HG00735.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.299-2512_299-2501d others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 40757902 | ||||||
| chr4:40758135 | G | A | 2 | a0002c0002t0001g0262 a0002c0002t0004g0261 |
2 | NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.299-2299G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758135 | |||||||
| chr4:40758142 | A | G | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-2292A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758142 | |||||||
| chr4:40758157 | T | C | 1 | a0001c0001t0013g0327 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.299-2277T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758157 | |||||||
| chr4:40758316 | A | C | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-2118A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758316 | |||||||
| chr4:40758426 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.299-2008C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758426 | |||||||
| chr4:40758654 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299-1780A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758654 | |||||||
| chr4:40758717 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0195 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.299-1717A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40758717 | |||||||
| chr4:40759028 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-1406C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759028 | |||||||
| chr4:40759075 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-1359C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759075 | |||||||
| chr4:40759096 | G | A | 2 | a0001c0013t0002g0153 a0015c0015t0040g0174 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-1338G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759096 | |||||||
| chr4:40759281 | G | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-1153G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759281 | |||||||
| chr4:40759285 | G | A | 3 | a0003c0003t0003g0029 a0003c0003t0003g0030 a0003c0003t0003g0231 |
3 | HG00733.hp2 HG01261.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.299-1149G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759285 | |||||||
| chr4:40759302 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.299-1132C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759302 | |||||||
| chr4:40759329 | A | T | 6 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-1105A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759329 | |||||||
| chr4:40759415 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.299-1019A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759415 | |||||||
| chr4:40759715 | C | G | 1 | a0002c0002t0001g0317 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-719C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759715 | |||||||
| chr4:40759792 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.299-642G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759792 | |||||||
| chr4:40759926 | A | C | 1 | a0001c0001t0004g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.299-508A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759926 | |||||||
| chr4:40759969 | C | T | 3 | a0001c0013t0002g0153 a0003c0003t0006g0165 a0015c0015t0040g0174 |
3 | HG02559.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299-465C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759969 | |||||||
| chr4:40759979 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(270): Show |
283 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.299-455A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40759979 | |||||||
| chr4:40760027 | G | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(258): Show |
271 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.299-407G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760027 | |||||||
| chr4:40760184 | G | T | 3 | a0001c0001t0010g0225 a0001c0001t0019g0223 a0001c0001t0019g0224 |
3 | HG02258.hp1 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.299-250G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760184 | |||||||
| chr4:40760217 | T | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-217T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760217 | |||||||
| chr4:40760228 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-206G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760228 | |||||||
| chr4:40760400 | A | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-34A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 2/11 | chr4 | 40760400 | |||||||
| chr4:40760610 | C | T | 3 | a0002c0002t0010g0136 a0002c0002t0010g0145 a0002c0002t0010g0166 |
3 | HG02717.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.357+118C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760610 | |||||||
| chr4:40760687 | A | AC | 18 | a0001c0001t0039g0230 a0001c0001t0045g0066 a0001c0001t0047g0074 others(15): Show |
18 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+197dupC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760687 | ||||||
| chr4:40760692 | G | T | 17 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0001c0013t0002g0153 others(14): Show |
17 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+200G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760692 | |||||||
| chr4:40760730 | A | C | 1 | a0002c0002t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.357+238A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760730 | |||||||
| chr4:40760730 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
152 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.357+238A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760730 | |||||||
| chr4:40760732 | A | G | 1 | a0003c0003t0003g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.357+240A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760732 | |||||||
| chr4:40760778 | T | C | 7 | a0001c0001t0002g0184 a0001c0001t0002g0190 a0001c0001t0002g0191 others(4): Show |
7 | HG01070.hp1 HG01074.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+286T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760778 | |||||||
| chr4:40760816 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.357+324T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760816 | |||||||
| chr4:40760819 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(137): Show |
145 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(142): Show |
intron_variant | MODIFIER | c.357+327G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760819 | |||||||
| chr4:40760862 | C | CA | 31 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0096 others(28): Show |
31 | HG00642.hp2 HG00733.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.358-290dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760862 | ||||||
| chr4:40760862 | CA | C | 21 | a0001c0001t0001g0112 a0001c0001t0001g0144 a0001c0001t0002g0219 others(18): Show |
21 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.358-290delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760862 | ||||||
| chr4:40760911 | CTCTTAAA | C | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-251_358-245del others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760911 | ||||||
| chr4:40760983 | C | G | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-188C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40760983 | |||||||
| chr4:40760996 | G | GT | 10 | a0001c0001t0001g0095 a0001c0001t0007g0241 a0001c0001t0007g0244 others(7): Show |
10 | HG02055.hp2 HG02486.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-165dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 40760996 | ||||||
| chr4:40761121 | G | A | 6 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(3): Show |
6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-50G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40761121 | |||||||
| chr4:40761151 | T | A | 1 | a0002c0002t0004g0274 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.358-20T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40761151 | |||||||
| chr4:40761153 | T | A | 1 | a0002c0002t0004g0274 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.358-18T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 3/11 | chr4 | 40761153 | |||||||
| chr4:40761305 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.488+4A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761305 | |||||||
| chr4:40761449 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.488+148A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761449 | |||||||
| chr4:40761600 | A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+299A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761600 | |||||||
| chr4:40761750 | A | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+449A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761750 | |||||||
| chr4:40761757 | T | C | 63 | a0001c0001t0001g0016 a0001c0001t0001g0138 a0001c0001t0001g0199 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.488+456T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40761757 | |||||||
| chr4:40762143 | A | T | 8 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(5): Show |
8 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+842A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40762143 | |||||||
| chr4:40762402 | C | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(251): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.488+1101C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40762402 | |||||||
| chr4:40762773 | T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+1472T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40762773 | |||||||
| chr4:40762798 | G | GATTGTGA others(28): Show |
1 | a0003c0003t0003g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.488+1500_488+1534d others(37): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40762798 | ||||||
| chr4:40762869 | A | AGATGATC others(22): Show |
18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+1605_488+1633d others(31): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40762869 | ||||||
| chr4:40763119 | G | T | 1 | a0002c0002t0014g0307 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.488+1818G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763119 | |||||||
| chr4:40763318 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.488+2017T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763318 | |||||||
| chr4:40763403 | T | TTGG | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(281): Show |
295 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.488+2103_488+2105d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40763403 | ||||||
| chr4:40763413 | A | T | 1 | a0001c0001t0002g0218 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.488+2112A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763413 | |||||||
| chr4:40763447 | C | T | 9 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(6): Show |
9 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.488+2146C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763447 | |||||||
| chr4:40763448 | G | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.488+2147G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763448 | |||||||
| chr4:40763448 | G | C | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+2147G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763448 | |||||||
| chr4:40763455 | T | C | 1 | a0002c0002t0001g0349 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.488+2154T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763455 | |||||||
| chr4:40763609 | A | T | 1 | a0001c0001t0013g0334 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.488+2308A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763609 | |||||||
| chr4:40763640 | A | C | 8 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(5): Show |
8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+2339A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763640 | |||||||
| chr4:40763735 | C | T | 1 | a0002c0002t0001g0352 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.488+2434C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40763735 | |||||||
| chr4:40764049 | T | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+2748T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764049 | |||||||
| chr4:40764056 | T | A | 18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+2755T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764056 | |||||||
| chr4:40764064 | T | A | 1 | a0001c0001t0018g0025 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.488+2763T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764064 | |||||||
| chr4:40764074 | AT | A | 8 | a0004c0004t0008g0068 a0004c0004t0008g0069 a0004c0004t0008g0070 others(5): Show |
8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+2780delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40764074 | ||||||
| chr4:40764081 | T | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.488+2780T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764081 | |||||||
| chr4:40764113 | C | A | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+2812C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764113 | |||||||
| chr4:40764227 | C | A | 18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.488+2926C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764227 | |||||||
| chr4:40764228 | T | C | 2 | a0002c0002t0001g0257 a0002c0002t0001g0275 |
2 | HG00544.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.488+2927T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764228 | |||||||
| chr4:40764228 | T | TC | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0259 others(6): Show |
9 | HG01099.hp2 HG01255.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.488+2933dupC | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40764228 | ||||||
| chr4:40764348 | C | T | 7 | a0003c0003t0003g0217 a0003c0003t0003g0226 a0003c0003t0015g0240 others(4): Show |
7 | HG00140.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+3047C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764348 | |||||||
| chr4:40764350 | A | C | 4 | a0003c0003t0015g0240 a0003c0003t0016g0239 a0003c0003t0016g0348 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+3049A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764350 | |||||||
| chr4:40764455 | A | T | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.488+3154A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764455 | |||||||
| chr4:40764480 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0154 a0001c0001t0001g0155 others(14): Show |
17 | HG01891.hp2 HG02280.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.488+3179C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764480 | |||||||
| chr4:40764481 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.488+3180G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764481 | |||||||
| chr4:40764597 | T | A | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.488+3296T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764597 | |||||||
| chr4:40764598 | A | C | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.488+3297A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764598 | |||||||
| chr4:40764600 | C | T | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+3299C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764600 | |||||||
| chr4:40764698 | A | G | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+3397A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764698 | |||||||
| chr4:40764765 | T | C | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.488+3464T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764765 | |||||||
| chr4:40764766 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488+3465G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764766 | |||||||
| chr4:40764900 | A | G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488+3599A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764900 | |||||||
| chr4:40764921 | G | A | 1 | a0006c0007t0048g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.488+3620G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764921 | |||||||
| chr4:40764960 | A | G | 1 | a0002c0002t0001g0360 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.488+3659A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40764960 | |||||||
| chr4:40765035 | G | A | 2 | a0003c0003t0003g0237 a0003c0003t0031g0031 |
2 | HG01255.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.488+3734G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765035 | |||||||
| chr4:40765087 | A | G | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+3786A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765087 | |||||||
| chr4:40765138 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.488+3837G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765138 | |||||||
| chr4:40765221 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(251): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.488+3920G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765221 | |||||||
| chr4:40765307 | A | C | 1 | a0003c0003t0011g0163 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.488+4006A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765307 | |||||||
| chr4:40765362 | C | G | 1 | a0003c0003t0016g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488+4061C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765362 | |||||||
| chr4:40765402 | G | A | 2 | a0001c0001t0004g0243 a0001c0001t0007g0242 |
2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.488+4101G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765402 | |||||||
| chr4:40765513 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.488+4212G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765513 | |||||||
| chr4:40765670 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.488+4369G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765670 | |||||||
| chr4:40765688 | C | T | 1 | a0002c0002t0005g0316 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.488+4387C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765688 | |||||||
| chr4:40765734 | C | G | 1 | a0001c0001t0009g0338 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.488+4433C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765734 | |||||||
| chr4:40765737 | G | T | 1 | a0001c0001t0009g0338 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.488+4436G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765737 | |||||||
| chr4:40765790 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.488+4489C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765790 | |||||||
| chr4:40765864 | A | G | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+4563A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765864 | |||||||
| chr4:40765873 | C | T | 1 | a0002c0002t0001g0303 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.488+4572C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765873 | |||||||
| chr4:40765893 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.488+4592G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765893 | |||||||
| chr4:40765943 | C | T | 71 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.488+4642C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40765943 | |||||||
| chr4:40766064 | A | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+4763A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766064 | |||||||
| chr4:40766286 | C | T | 2 | a0001c0001t0009g0193 a0001c0001t0017g0180 |
2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.488+4985C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766286 | |||||||
| chr4:40766291 | AG | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(251): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.488+4993delG | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40766291 | ||||||
| chr4:40766416 | A | G | 10 | a0001c0001t0039g0230 a0003c0003t0006g0049 a0003c0003t0006g0059 others(7): Show |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+5115A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766416 | |||||||
| chr4:40766506 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488+5205G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766506 | |||||||
| chr4:40766673 | G | A | 4 | a0003c0003t0015g0240 a0003c0003t0016g0239 a0003c0003t0016g0348 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.488+5372G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766673 | |||||||
| chr4:40766705 | C | T | 1 | a0003c0003t0006g0362 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.488+5404C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766705 | |||||||
| chr4:40766752 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(251): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.488+5451G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40766752 | |||||||
| chr4:40767061 | G | C | 2 | a0002c0002t0001g0355 a0002c0002t0010g0097 |
2 | HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.488+5760G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767061 | |||||||
| chr4:40767310 | G | A | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+6009G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767310 | |||||||
| chr4:40767367 | T | C | 2 | a0001c0001t0002g0198 a0001c0001t0002g0219 |
2 | NA19063.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.488+6066T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767367 | |||||||
| chr4:40767412 | C | T | 1 | a0002c0002t0001g0355 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.488+6111C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767412 | |||||||
| chr4:40767893 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.489-6372C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767893 | |||||||
| chr4:40767918 | G | A | 1 | a0003c0003t0003g0340 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.489-6347G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40767918 | |||||||
| chr4:40768109 | G | T | 4 | a0002c0002t0001g0015 a0002c0002t0001g0169 a0002c0002t0002g0015 others(1): Show |
4 | NA18993.hp2 NA19011.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-6156G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768109 | |||||||
| chr4:40768204 | C | CT | 9 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0140 others(6): Show |
9 | NA18944.hp1 NA18985.hp2 NA18988.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-6046dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40768204 | ||||||
| chr4:40768204 | CT | C | 71 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0050 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.489-6046delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40768204 | ||||||
| chr4:40768208 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.489-6057T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768208 | |||||||
| chr4:40768209 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(4): Show |
7 | HG02257.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-6056T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768209 | |||||||
| chr4:40768240 | C | T | 2 | a0003c0003t0006g0165 a0003c0003t0006g0363 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.489-6025C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768240 | |||||||
| chr4:40768436 | C | T | 14 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(11): Show |
14 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.489-5829C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768436 | |||||||
| chr4:40768486 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489-5779G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768486 | |||||||
| chr4:40768669 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(251): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.489-5596G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768669 | |||||||
| chr4:40768966 | C | G | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489-5299C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40768966 | |||||||
| chr4:40769076 | C | G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489-5189C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769076 | |||||||
| chr4:40769253 | T | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.489-5012T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769253 | |||||||
| chr4:40769322 | T | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.489-4943T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769322 | |||||||
| chr4:40769347 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489-4918A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769347 | |||||||
| chr4:40769375 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.489-4890C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769375 | |||||||
| chr4:40769376 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.489-4889G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769376 | |||||||
| chr4:40769519 | G | A | 2 | a0003c0003t0006g0165 a0003c0003t0006g0363 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.489-4746G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769519 | |||||||
| chr4:40769673 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(125): Show |
138 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.489-4592T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769673 | |||||||
| chr4:40769714 | A | G | 8 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(5): Show |
8 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-4551A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769714 | |||||||
| chr4:40769815 | C | T | 1 | a0008c0008t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489-4450C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769815 | |||||||
| chr4:40769908 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-4357C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769908 | |||||||
| chr4:40769975 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489-4290C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769975 | |||||||
| chr4:40769983 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489-4282G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769983 | |||||||
| chr4:40769990 | T | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.489-4275T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769990 | |||||||
| chr4:40769997 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489-4268G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769997 | |||||||
| chr4:40769997 | G | T | 1 | a0003c0003t0003g0030 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.489-4268G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40769997 | |||||||
| chr4:40770012 | C | A | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.489-4253C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770012 | |||||||
| chr4:40770070 | C | T | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-4195C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770070 | |||||||
| chr4:40770094 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.489-4171T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770094 | |||||||
| chr4:40770188 | T | A | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.489-4077T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770188 | |||||||
| chr4:40770210 | C | CA | 12 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0002c0002t0001g0278 others(9): Show |
12 | HG02071.hp2 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.489-4036dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40770210 | ||||||
| chr4:40770210 | CA | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
247 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.489-4036delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40770210 | ||||||
| chr4:40770210 | CAA | C | 14 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0001g0108 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.489-4037_489-4036d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40770210 | ||||||
| chr4:40770230 | G | A | 1 | a0002c0002t0001g0277 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.489-4035G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770230 | |||||||
| chr4:40770284 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.489-3981G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770284 | |||||||
| chr4:40770446 | A | G | 1 | a0003c0003t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.489-3819A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770446 | |||||||
| chr4:40770497 | C | T | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-3768C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770497 | |||||||
| chr4:40770532 | G | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
130 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.489-3733G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770532 | |||||||
| chr4:40770934 | C | T | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-3331C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770934 | |||||||
| chr4:40770942 | T | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
193 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.489-3323T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770942 | |||||||
| chr4:40770983 | G | A | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-3282G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40770983 | |||||||
| chr4:40771046 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.489-3219C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771046 | |||||||
| chr4:40771183 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.489-3082G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771183 | |||||||
| chr4:40771241 | T | C | 9 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(6): Show |
9 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.489-3024T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771241 | |||||||
| chr4:40771260 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-3005C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771260 | |||||||
| chr4:40771265 | A | G | 1 | a0002c0002t0001g0260 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.489-3000A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771265 | |||||||
| chr4:40771500 | A | C | 1 | a0001c0001t0009g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.489-2765A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771500 | |||||||
| chr4:40771591 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.489-2674T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771591 | |||||||
| chr4:40771648 | C | A | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.489-2617C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771648 | |||||||
| chr4:40771662 | A | C | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.489-2603A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771662 | |||||||
| chr4:40771745 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.489-2520A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771745 | |||||||
| chr4:40771842 | T | C | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489-2423T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771842 | |||||||
| chr4:40771952 | A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.489-2313A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40771952 | |||||||
| chr4:40772059 | C | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(253): Show |
266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.489-2206C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772059 | |||||||
| chr4:40772073 | C | A | 2 | a0002c0002t0001g0253 a0002c0002t0001g0254 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.489-2192C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772073 | |||||||
| chr4:40772665 | A | T | 2 | a0001c0001t0001g0007 a0012c0023t0001g0007 |
2 | HG00408.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.489-1600A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772665 | |||||||
| chr4:40772716 | C | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.489-1549C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772716 | |||||||
| chr4:40772815 | A | C | 1 | a0003c0003t0003g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.489-1450A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40772815 | |||||||
| chr4:40773020 | G | A | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.489-1245G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773020 | |||||||
| chr4:40773117 | C | T | 3 | a0002c0002t0001g0262 a0002c0002t0001g0314 a0002c0002t0004g0261 |
3 | NA18961.hp1 NA19004.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.489-1148C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773117 | |||||||
| chr4:40773176 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(277): Show |
290 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.489-1089C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773176 | |||||||
| chr4:40773420 | C | T | 2 | a0002c0002t0001g0355 a0002c0002t0010g0097 |
2 | HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.489-845C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773420 | |||||||
| chr4:40773421 | G | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
193 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.489-844G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773421 | |||||||
| chr4:40773503 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.489-762C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773503 | |||||||
| chr4:40773661 | C | T | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.489-604C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773661 | |||||||
| chr4:40773682 | C | CA | 11 | a0001c0001t0002g0205 a0001c0001t0045g0066 a0001c0001t0047g0074 others(8): Show |
11 | HG02280.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.489-568dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40773682 | ||||||
| chr4:40773682 | CA | C | 11 | a0001c0001t0001g0058 a0001c0001t0001g0183 a0001c0001t0004g0243 others(8): Show |
11 | HG01934.hp2 HG02486.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.489-568delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 40773682 | ||||||
| chr4:40773724 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(259): Show |
272 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.489-541C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773724 | |||||||
| chr4:40773947 | C | T | 10 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-318C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773947 | |||||||
| chr4:40773991 | T | G | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.489-274T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40773991 | |||||||
| chr4:40774084 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.489-181C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 4/11 | chr4 | 40774084 | |||||||
| chr4:40774511 | C | A | 1 | a0002c0002t0005g0304 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.641+94C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/11 | chr4 | 40774511 | |||||||
| chr4:40774516 | C | T | 1 | a0003c0003t0016g0239 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.641+99C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/11 | chr4 | 40774516 | |||||||
| chr4:40774686 | T | G | 4 | a0001c0001t0001g0229 a0001c0001t0002g0186 a0001c0001t0002g0187 others(1): Show |
4 | NA18944.hp2 NA18975.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-81T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 5/11 | chr4 | 40774686 | |||||||
| chr4:40774961 | A | G | 7 | a0002c0002t0001g0355 a0002c0002t0010g0097 a0002c0002t0010g0120 others(4): Show |
7 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.825+11A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40774961 | |||||||
| chr4:40775063 | G | A | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.825+113G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775063 | |||||||
| chr4:40775130 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(264): Show |
277 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.825+180G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775130 | |||||||
| chr4:40775194 | T | A | 1 | a0005c0005t0001g0280 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.825+244T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775194 | |||||||
| chr4:40775229 | C | T | 8 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(5): Show |
8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.825+279C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775229 | |||||||
| chr4:40775318 | A | G | 1 | a0002c0002t0001g0278 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.825+368A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775318 | |||||||
| chr4:40775332 | A | C | 4 | a0003c0003t0003g0340 a0003c0003t0003g0343 a0003c0003t0003g0344 others(1): Show |
4 | HG01081.hp2 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+382A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775332 | |||||||
| chr4:40775430 | T | A | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.825+480T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775430 | |||||||
| chr4:40775442 | G | A | 1 | a0003c0003t0006g0363 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.825+492G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775442 | |||||||
| chr4:40775453 | G | A | 4 | a0002c0002t0010g0120 a0002c0002t0010g0136 a0002c0002t0010g0145 others(1): Show |
4 | HG02486.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.825+503G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775453 | |||||||
| chr4:40775785 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.826-264A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775785 | |||||||
| chr4:40775928 | C | G | 1 | a0003c0003t0022g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.826-121C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775928 | |||||||
| chr4:40775929 | T | C | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826-120T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775929 | |||||||
| chr4:40775944 | C | A | 83 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.826-105C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40775944 | |||||||
| chr4:40776009 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.826-40C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 6/11 | chr4 | 40776009 | |||||||
| chr4:40776315 | G | A | 3 | a0006c0007t0028g0043 a0006c0007t0030g0045 a0006c0007t0048g0236 |
3 | HG01243.hp1 HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1036+56G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776315 | |||||||
| chr4:40776333 | A | G | 2 | a0001c0001t0039g0230 a0001c0013t0002g0153 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1036+74A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776333 | |||||||
| chr4:40776391 | T | C | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1036+132T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776391 | |||||||
| chr4:40776444 | G | A | 8 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(5): Show |
8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+185G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776444 | |||||||
| chr4:40776529 | GTATCATT others(17): Show |
G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+287_1036+310d others(26): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40776529 | ||||||
| chr4:40776622 | C | CT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0133 others(2): Show |
6 | NA18946.hp1 NA18956.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+374dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40776622 | ||||||
| chr4:40776693 | A | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+434A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776693 | |||||||
| chr4:40776841 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1036+582C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776841 | |||||||
| chr4:40776898 | G | A | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1036+639G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40776898 | |||||||
| chr4:40777094 | C | T | 1 | a0003c0003t0006g0363 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1036+835C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777094 | |||||||
| chr4:40777328 | T | A | 31 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0121 others(28): Show |
32 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1036+1069T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777328 | |||||||
| chr4:40777329 | T | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(154): Show |
167 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.1036+1070T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777329 | |||||||
| chr4:40777341 | T | G | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1036+1082T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777341 | |||||||
| chr4:40777379 | C | T | 7 | a0002c0002t0001g0355 a0002c0002t0010g0097 a0002c0002t0010g0120 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+1120C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777379 | |||||||
| chr4:40777462 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+1203C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777462 | |||||||
| chr4:40777579 | G | A | 4 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(1): Show |
4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+1320G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777579 | |||||||
| chr4:40777591 | C | T | 1 | a0003c0003t0003g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1036+1332C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777591 | |||||||
| chr4:40777783 | T | G | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+1524T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777783 | |||||||
| chr4:40777784 | G | T | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+1525G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777784 | |||||||
| chr4:40777839 | A | G | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+1580A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777839 | |||||||
| chr4:40777839 | ATCC | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+1585_1036+158 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40777839 | ||||||
| chr4:40777951 | G | A | 71 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1036+1692G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40777951 | |||||||
| chr4:40778093 | T | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1036+1834T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778093 | |||||||
| chr4:40778106 | C | T | 1 | a0001c0001t0047g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1036+1847C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778106 | |||||||
| chr4:40778159 | G | GA | 7 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(4): Show |
7 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+1903dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40778159 | ||||||
| chr4:40778347 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
187 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.1036+2088T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778347 | |||||||
| chr4:40778420 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1036+2161G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778420 | |||||||
| chr4:40778444 | G | A | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1036+2185G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778444 | |||||||
| chr4:40778493 | G | A | 2 | a0003c0003t0006g0165 a0003c0003t0006g0363 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1036+2234G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778493 | |||||||
| chr4:40778623 | CCT | C | 6 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(3): Show |
6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+2365_1036+236 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778623 | |||||||
| chr4:40778626 | A | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+2367A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778626 | |||||||
| chr4:40778627 | G | A | 6 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(3): Show |
6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+2368G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778627 | |||||||
| chr4:40778932 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1036+2673T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778932 | |||||||
| chr4:40778971 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(275): Show |
288 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1036+2712G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40778971 | |||||||
| chr4:40779017 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1036+2758G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779017 | |||||||
| chr4:40779094 | A | C | 2 | a0002c0002t0001g0311 a0002c0002t0004g0301 |
2 | NA18956.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1036+2835A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779094 | |||||||
| chr4:40779164 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1036+2905A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779164 | |||||||
| chr4:40779381 | A | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+3122A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779381 | |||||||
| chr4:40779601 | C | G | 6 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(3): Show |
6 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+3342C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779601 | |||||||
| chr4:40779601 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
183 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.1036+3342C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779601 | |||||||
| chr4:40779738 | A | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(24): Show |
29 | HG00558.hp1 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1036+3479A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779738 | |||||||
| chr4:40779896 | A | G | 8 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(5): Show |
8 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+3637A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40779896 | |||||||
| chr4:40780051 | C | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
130 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1036+3792C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780051 | |||||||
| chr4:40780066 | C | T | 1 | a0001c0001t0020g0324 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1036+3807C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780066 | |||||||
| chr4:40780234 | C | T | 4 | a0001c0001t0002g0220 a0001c0001t0010g0225 a0001c0001t0019g0223 others(1): Show |
4 | HG02258.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+3975C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780234 | |||||||
| chr4:40780269 | G | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+4010G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780269 | |||||||
| chr4:40780282 | A | AAATC | 18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1036+4047_1036+405 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780282 | ||||||
| chr4:40780284 | A | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1036+4025A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780284 | |||||||
| chr4:40780317 | A | G | 1 | a0001c0001t0004g0117 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1036+4058A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780317 | |||||||
| chr4:40780489 | C | T | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1036+4230C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780489 | |||||||
| chr4:40780630 | G | A | 1 | a0001c0001t0004g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1036+4371G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780630 | |||||||
| chr4:40780668 | G | A | 10 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(7): Show |
10 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+4409G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780668 | |||||||
| chr4:40780669 | G | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+4410G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780669 | |||||||
| chr4:40780728 | A | G | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+4469A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780728 | |||||||
| chr4:40780754 | T | TAC | 34 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
35 | HG00735.hp2 HG01358.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.1036+4527_1036+452 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | ||||||
| chr4:40780754 | T | TACAC | 13 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0090 others(10): Show |
14 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.1036+4525_1036+452 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | ||||||
| chr4:40780754 | T | TACACAC | 8 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0100 others(5): Show |
8 | HG00544.hp1 HG01928.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036+4523_1036+452 others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | ||||||
| chr4:40780754 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0099 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1036+4519_1036+452 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | ||||||
| chr4:40780754 | TAC | T | 6 | a0002c0002t0001g0254 a0002c0002t0001g0255 a0002c0002t0001g0257 others(3): Show |
6 | HG00544.hp2 HG01978.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4527_1036+452 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | ||||||
| chr4:40780754 | TACAC | T | 2 | a0002c0002t0001g0300 a0002c0002t0002g0018 |
3 | HG02886.hp2 NA18906.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1036+4525_1036+452 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780754 | ||||||
| chr4:40780774 | CACACACA others(7): Show |
C | 7 | a0001c0001t0047g0074 a0004c0004t0008g0070 a0004c0004t0008g0071 others(4): Show |
7 | HG02280.hp2 HG02630.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+4521_1036+453 others(18): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780774 | ||||||
| chr4:40780776 | CACACACA others(5): Show |
C | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1036+4523_1036+453 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780776 | ||||||
| chr4:40780778 | CACACACA others(9): Show |
C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+4521_1036+453 others(20): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780778 | ||||||
| chr4:40780782 | CACACAT | C | 6 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(3): Show |
6 | HG02074.hp1 NA18943.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4531_1036+453 others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780782 | ||||||
| chr4:40780782 | CACACATA others(5): Show |
C | 1 | a0003c0003t0003g0237 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1036+4525_1036+453 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780782 | ||||||
| chr4:40780782 | CACACATA others(7): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1036+4525_1036+453 others(18): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780782 | ||||||
| chr4:40780784 | CACAT | C | 37 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(34): Show |
37 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.1036+4529_1036+453 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780784 | ||||||
| chr4:40780784 | CACATACA others(3): Show |
C | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1036+4527_1036+453 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780784 | ||||||
| chr4:40780784 | CACATACA others(9): Show |
C | 5 | a0001c0001t0002g0208 a0001c0001t0002g0210 a0001c0001t0002g0216 others(2): Show |
5 | HG01192.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+4527_1036+454 others(20): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780784 | ||||||
| chr4:40780786 | C | T | 1 | a0002c0002t0001g0321 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1036+4527C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780786 | |||||||
| chr4:40780786 | CAT | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(41): Show |
45 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1036+4529_1036+453 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780786 | ||||||
| chr4:40780786 | CATACACA others(5): Show |
C | 3 | a0001c0001t0002g0207 a0001c0001t0002g0219 a0011c0021t0002g0084 |
3 | HG02080.hp2 NA19063.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1036+4531_1036+454 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780786 | ||||||
| chr4:40780786 | CATACACA others(7): Show |
C | 11 | a0001c0001t0002g0203 a0001c0001t0002g0342 a0001c0001t0002g0353 others(8): Show |
11 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036+4531_1036+454 others(18): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780786 | ||||||
| chr4:40780788 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
160 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1036+4529T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780788 | |||||||
| chr4:40780788 | TACAC | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0256 |
3 | NA18949.hp2 NA18957.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1036+4531_1036+453 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780788 | ||||||
| chr4:40780790 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0033g0082 a0002c0002t0001g0270 |
3 | HG03139.hp2 HG03540.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1036+4531C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780790 | |||||||
| chr4:40780790 | CACATATA others(3): Show |
C | 1 | a0001c0001t0002g0113 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1036+4533_1036+454 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780790 | ||||||
| chr4:40780790 | CACATATA others(5): Show |
C | 1 | a0001c0001t0001g0202 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1036+4533_1036+454 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780790 | ||||||
| chr4:40780792 | C | CAT | 6 | a0002c0002t0001g0004 a0002c0002t0001g0276 a0002c0002t0001g0285 others(3): Show |
8 | HG00438.hp2 HG04115.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036+4554_1036+455 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780792 | ||||||
| chr4:40780792 | C | T | 6 | a0001c0001t0039g0230 a0001c0001t0045g0066 a0002c0002t0001g0270 others(3): Show |
6 | HG00438.hp1 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+4533C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780792 | |||||||
| chr4:40780792 | CATAT | C | 3 | a0001c0001t0001g0179 a0003c0003t0011g0162 a0003c0003t0025g0161 |
3 | HG01123.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1036+4552_1036+455 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780792 | ||||||
| chr4:40780794 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
129 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.1036+4535T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780794 | |||||||
| chr4:40780796 | T | C | 91 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1036+4537T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780796 | |||||||
| chr4:40780798 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
108 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1036+4539T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780798 | |||||||
| chr4:40780800 | T | C | 37 | a0001c0001t0001g0076 a0001c0001t0001g0093 a0001c0001t0001g0099 others(34): Show |
37 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1036+4541T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780800 | |||||||
| chr4:40780802 | T | C | 5 | a0001c0001t0001g0310 a0001c0001t0002g0353 a0001c0001t0018g0026 others(2): Show |
5 | HG00423.hp1 HG01074.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+4543T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780802 | |||||||
| chr4:40780803 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+4546_1036+455 others(17): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780803 | ||||||
| chr4:40780804 | T | C | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1036+4545T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780804 | |||||||
| chr4:40780804 | TATATATA others(2): Show |
T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(28): Show |
31 | HG00597.hp2 HG01070.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1036+4546_1036+455 others(13): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780804 | |||||||
| chr4:40780805 | ATATATAT others(2): Show |
A | 8 | a0001c0001t0002g0063 a0001c0001t0002g0196 a0001c0001t0002g0197 others(5): Show |
8 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036+4548_1036+455 others(13): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780805 | ||||||
| chr4:40780805 | ATATATAT others(3): Show |
A | 1 | a0003c0003t0003g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1036+4548_1036+455 others(14): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780805 | ||||||
| chr4:40780805 | ATATATAT others(5): Show |
A | 3 | a0001c0001t0007g0241 a0001c0001t0007g0246 a0001c0001t0007g0247 |
3 | NA18995.hp2 NA19004.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1036+4548_1036+455 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780805 | ||||||
| chr4:40780807 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0007g0245 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1036+4550_1036+456 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780807 | ||||||
| chr4:40780809 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0007g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1036+4552_1036+456 others(16): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780809 | ||||||
| chr4:40780811 | A | T | 1 | a0002c0002t0001g0005 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1036+4552A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780811 | |||||||
| chr4:40780811 | ATAT | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0003c0003t0003g0028 others(12): Show |
15 | HG00408.hp1 HG00733.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1036+4554_1036+455 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780811 | ||||||
| chr4:40780812 | TA | T | 15 | a0001c0001t0001g0057 a0001c0001t0001g0172 a0001c0001t0002g0203 others(12): Show |
15 | HG00738.hp1 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1036+4554delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780812 | |||||||
| chr4:40780813 | A | AT | 8 | a0002c0002t0001g0253 a0002c0002t0001g0254 a0002c0002t0001g0283 others(5): Show |
8 | HG02559.hp2 HG03834.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+4578dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | ||||||
| chr4:40780813 | A | T | 16 | a0001c0001t0002g0113 a0001c0001t0002g0219 a0001c0001t0036g0209 others(13): Show |
17 | HG00597.hp1 HG01192.hp1 HG03209.hp2 others(14): Show |
intron_variant | MODIFIER | c.1036+4554A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780813 | |||||||
| chr4:40780813 | AT | A | 24 | a0001c0001t0001g0146 a0001c0001t0002g0101 a0001c0001t0002g0342 others(21): Show |
24 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1036+4578delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | ||||||
| chr4:40780813 | ATT | A | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(39): Show |
45 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1036+4577_1036+457 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | ||||||
| chr4:40780813 | ATTT | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0144 others(3): Show |
6 | HG00558.hp1 HG01358.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+4576_1036+457 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | ||||||
| chr4:40780813 | ATTTT | A | 6 | a0002c0002t0001g0355 a0002c0002t0010g0097 a0002c0002t0010g0136 others(3): Show |
6 | HG02055.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4575_1036+457 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40780813 | ||||||
| chr4:40780814 | T | TA | 5 | a0001c0001t0001g0093 a0001c0001t0004g0117 a0001c0001t0009g0332 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+4555_1036+455 others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780814 | |||||||
| chr4:40780814 | T | TATA | 3 | a0001c0001t0001g0076 a0001c0001t0001g0310 a0002c0002t0001g0293 |
3 | HG00423.hp1 HG01346.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1036+4555_1036+455 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780814 | |||||||
| chr4:40780815 | T | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(63): Show |
70 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1036+4556T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780815 | |||||||
| chr4:40780816 | T | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0310 a0001c0001t0004g0117 others(4): Show |
7 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+4557T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780816 | |||||||
| chr4:40780817 | T | A | 25 | a0001c0001t0001g0114 a0001c0001t0001g0125 a0001c0001t0001g0126 others(22): Show |
25 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1036+4558T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780817 | |||||||
| chr4:40780818 | T | A | 2 | a0001c0001t0009g0332 a0002c0002t0010g0120 |
2 | HG02004.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1036+4559T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780818 | |||||||
| chr4:40780819 | T | A | 3 | a0001c0001t0012g0175 a0013c0009t0007g0325 a0015c0015t0040g0174 |
3 | HG02280.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1036+4560T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780819 | |||||||
| chr4:40780820 | T | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1036+4561T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780820 | |||||||
| chr4:40780859 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+4600G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780859 | |||||||
| chr4:40780868 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+4609G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780868 | |||||||
| chr4:40780889 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+4630G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780889 | |||||||
| chr4:40780922 | C | A | 2 | a0001c0001t0002g0196 a0001c0001t0002g0197 |
2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1036+4663C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780922 | |||||||
| chr4:40780926 | T | G | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1036+4667T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40780926 | |||||||
| chr4:40781064 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1036+4805C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781064 | |||||||
| chr4:40781098 | C | A | 1 | a0002c0002t0002g0018 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1036+4839C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781098 | |||||||
| chr4:40781181 | C | T | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+4922C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781181 | |||||||
| chr4:40781256 | G | T | 1 | a0003c0003t0022g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1036+4997G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781256 | |||||||
| chr4:40781263 | T | C | 14 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(11): Show |
14 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1036+5004T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781263 | |||||||
| chr4:40781447 | T | G | 1 | a0001c0001t0002g0196 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1036+5188T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781447 | |||||||
| chr4:40781520 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1036+5261C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781520 | |||||||
| chr4:40781553 | A | C | 2 | a0003c0003t0006g0165 a0003c0003t0006g0363 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1036+5294A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781553 | |||||||
| chr4:40781612 | A | G | 1 | a0002c0002t0001g0321 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1036+5353A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781612 | |||||||
| chr4:40781824 | AG | A | 7 | a0002c0002t0001g0355 a0002c0002t0010g0097 a0002c0002t0010g0120 others(4): Show |
7 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+5566delG | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40781824 | |||||||
| chr4:40782139 | C | T | 7 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(4): Show |
7 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+5880C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782139 | |||||||
| chr4:40782236 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1036+5977A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782236 | |||||||
| chr4:40782327 | C | A | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1036+6068C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782327 | |||||||
| chr4:40782327 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA19064.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1036+6068C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782327 | |||||||
| chr4:40782392 | C | T | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+6133C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782392 | |||||||
| chr4:40782430 | T | G | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+6171T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782430 | |||||||
| chr4:40782547 | CA | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
156 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1036+6303delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40782547 | ||||||
| chr4:40782564 | A | G | 1 | a0001c0001t0041g0248 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1036+6305A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782564 | |||||||
| chr4:40782609 | C | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+6350C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782609 | |||||||
| chr4:40782791 | C | T | 1 | a0003c0003t0003g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1036+6532C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782791 | |||||||
| chr4:40782921 | G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1036+6662G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40782921 | |||||||
| chr4:40783088 | T | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1036+6829T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783088 | |||||||
| chr4:40783157 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1036+6898C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783157 | |||||||
| chr4:40783229 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
187 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.1036+6970A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783229 | |||||||
| chr4:40783404 | T | C | 8 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(5): Show |
8 | HG02486.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+7145T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783404 | |||||||
| chr4:40783487 | G | GA | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(262): Show |
275 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.1037-7109dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40783487 | ||||||
| chr4:40783545 | T | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
5 | HG01891.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-7057T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783545 | |||||||
| chr4:40783715 | G | A | 1 | a0003c0003t0006g0363 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1037-6887G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783715 | |||||||
| chr4:40783724 | G | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-6878G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783724 | |||||||
| chr4:40783846 | TA | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0133 a0001c0001t0002g0219 others(7): Show |
10 | HG01074.hp1 HG01074.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-6741delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40783846 | ||||||
| chr4:40783847 | A | T | 66 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1037-6755A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783847 | |||||||
| chr4:40783848 | A | T | 4 | a0001c0001t0002g0219 a0001c0001t0002g0342 a0001c0001t0041g0248 others(1): Show |
4 | HG01074.hp1 HG01074.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-6754A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40783848 | |||||||
| chr4:40784092 | T | C | 1 | a0003c0003t0003g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1037-6510T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784092 | |||||||
| chr4:40784175 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1037-6427G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784175 | |||||||
| chr4:40784318 | T | C | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1037-6284T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784318 | |||||||
| chr4:40784331 | A | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(24): Show |
29 | HG00558.hp1 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1037-6271A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784331 | |||||||
| chr4:40784439 | C | T | 5 | a0001c0001t0002g0205 a0001c0001t0002g0220 a0001c0001t0010g0225 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-6163C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784439 | |||||||
| chr4:40784562 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1037-6040C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784562 | |||||||
| chr4:40784816 | T | C | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-5786T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784816 | |||||||
| chr4:40784834 | G | A | 6 | a0001c0001t0039g0230 a0003c0003t0014g0167 a0003c0003t0015g0240 others(3): Show |
6 | HG02965.hp1 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-5768G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784834 | |||||||
| chr4:40784942 | A | G | 11 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(8): Show |
11 | HG02486.hp2 HG02970.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.1037-5660A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40784942 | |||||||
| chr4:40785035 | A | AGTT | 5 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-5551_1037-554 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40785035 | ||||||
| chr4:40785129 | G | T | 1 | a0003c0003t0022g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1037-5473G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785129 | |||||||
| chr4:40785138 | C | G | 1 | a0002c0002t0002g0306 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1037-5464C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785138 | |||||||
| chr4:40785201 | A | AT | 9 | a0001c0001t0001g0023 a0001c0001t0001g0099 a0002c0002t0001g0254 others(6): Show |
9 | HG01258.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1037-5387dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40785201 | ||||||
| chr4:40785212 | T | G | 1 | a0001c0001t0005g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1037-5390T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785212 | |||||||
| chr4:40785294 | G | A | 4 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(1): Show |
4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-5308G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785294 | |||||||
| chr4:40785362 | T | C | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-5240T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785362 | |||||||
| chr4:40785518 | G | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(269): Show |
282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1037-5084G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785518 | |||||||
| chr4:40785561 | A | G | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-5041A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785561 | |||||||
| chr4:40785607 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-4995C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785607 | |||||||
| chr4:40785641 | G | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-4961G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785641 | |||||||
| chr4:40785676 | A | AATGAC | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(267): Show |
280 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1037-4924_1037-492 others(9): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40785676 | ||||||
| chr4:40785736 | G | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(275): Show |
288 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1037-4866G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785736 | |||||||
| chr4:40785928 | C | T | 4 | a0003c0003t0015g0240 a0003c0003t0016g0239 a0003c0003t0016g0348 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-4674C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40785928 | |||||||
| chr4:40786123 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1037-4479G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786123 | |||||||
| chr4:40786193 | T | C | 75 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1037-4409T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786193 | |||||||
| chr4:40786527 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(269): Show |
282 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1037-4075A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786527 | |||||||
| chr4:40786662 | A | G | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-3940A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786662 | |||||||
| chr4:40786730 | T | C | 1 | a0002c0002t0001g0269 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1037-3872T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40786730 | |||||||
| chr4:40787036 | G | GA | 32 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(29): Show |
32 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1037-3554dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787036 | ||||||
| chr4:40787036 | G | GAA | 27 | a0001c0001t0001g0229 a0001c0001t0002g0113 a0001c0001t0002g0186 others(24): Show |
27 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1037-3555_1037-355 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787036 | ||||||
| chr4:40787036 | G | GAAA | 6 | a0001c0001t0002g0203 a0001c0001t0002g0208 a0001c0001t0002g0210 others(3): Show |
6 | HG00738.hp1 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-3556_1037-355 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787036 | ||||||
| chr4:40787044 | A | G | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-3558A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787044 | |||||||
| chr4:40787185 | G | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-3417G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787185 | |||||||
| chr4:40787324 | C | G | 1 | a0006c0007t0048g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1037-3278C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787324 | |||||||
| chr4:40787352 | A | T | 18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1037-3250A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787352 | |||||||
| chr4:40787353 | AG | A | 18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1037-3248delG | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787353 | |||||||
| chr4:40787375 | AAG | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-3225_1037-322 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40787375 | ||||||
| chr4:40787676 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1037-2926C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787676 | |||||||
| chr4:40787858 | G | A | 1 | a0003c0003t0016g0348 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1037-2744G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787858 | |||||||
| chr4:40787897 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1037-2705C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787897 | |||||||
| chr4:40787968 | G | A | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1037-2634G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787968 | |||||||
| chr4:40787971 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
185 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.1037-2631A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787971 | |||||||
| chr4:40787983 | G | C | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-2619G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40787983 | |||||||
| chr4:40788447 | A | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-2155A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788447 | |||||||
| chr4:40788664 | T | A | 18 | a0001c0001t0001g0330 a0001c0001t0009g0193 a0001c0001t0009g0328 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1037-1938T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788664 | |||||||
| chr4:40788737 | C | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-1865C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788737 | |||||||
| chr4:40788828 | T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1037-1774T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788828 | |||||||
| chr4:40788943 | C | T | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-1659C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40788943 | |||||||
| chr4:40789043 | G | C | 5 | a0001c0001t0001g0229 a0001c0001t0002g0186 a0001c0001t0002g0187 others(2): Show |
5 | NA18944.hp2 NA18975.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-1559G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789043 | |||||||
| chr4:40789135 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
202 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.1037-1467C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789135 | |||||||
| chr4:40789139 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(151): Show |
164 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.1037-1463C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789139 | |||||||
| chr4:40789253 | T | C | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1037-1349T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789253 | |||||||
| chr4:40789348 | A | G | 4 | a0003c0003t0003g0340 a0003c0003t0003g0343 a0003c0003t0003g0344 others(1): Show |
4 | HG01081.hp2 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-1254A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789348 | |||||||
| chr4:40789355 | G | A | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-1247G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789355 | |||||||
| chr4:40789491 | G | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-1111G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789491 | |||||||
| chr4:40789615 | T | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(270): Show |
283 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1037-987T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789615 | |||||||
| chr4:40789705 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1037-897A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789705 | |||||||
| chr4:40789930 | A | G | 5 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-672A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789930 | |||||||
| chr4:40789934 | A | C | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-668A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789934 | |||||||
| chr4:40789990 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(255): Show |
268 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1037-612G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40789990 | |||||||
| chr4:40790013 | T | C | 1 | a0002c0002t0001g0287 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1037-589T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790013 | |||||||
| chr4:40790064 | C | CT | 11 | a0001c0001t0001g0053 a0001c0001t0001g0085 a0001c0001t0001g0088 others(8): Show |
11 | HG01169.hp2 HG02818.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1037-520dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | ||||||
| chr4:40790064 | C | CTT | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
156 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1037-521_1037-520d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | ||||||
| chr4:40790064 | C | CTTT | 12 | a0001c0001t0001g0110 a0001c0001t0001g0154 a0001c0001t0001g0157 others(9): Show |
12 | HG01099.hp2 HG02965.hp1 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.1037-522_1037-520d others(5): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | ||||||
| chr4:40790064 | C | CTTTT | 15 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(12): Show |
15 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037-523_1037-520d others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | ||||||
| chr4:40790064 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0033g0082 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1037-538C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790064 | |||||||
| chr4:40790064 | CT | C | 64 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1037-520delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 40790064 | ||||||
| chr4:40790135 | C | G | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-467C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790135 | |||||||
| chr4:40790233 | T | C | 11 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(8): Show |
11 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1037-369T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790233 | |||||||
| chr4:40790323 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1037-279G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790323 | |||||||
| chr4:40790324 | T | C | 1 | a0002c0002t0004g0301 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1037-278T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790324 | |||||||
| chr4:40790446 | G | A | 62 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1037-156G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790446 | |||||||
| chr4:40790482 | T | A | 13 | a0001c0001t0018g0025 a0001c0001t0018g0026 a0001c0001t0045g0066 others(10): Show |
13 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1037-120T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 7/11 | chr4 | 40790482 | |||||||
| chr4:40790780 | T | G | 1 | a0002c0002t0001g0298 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1180+35T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40790780 | |||||||
| chr4:40790797 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1180+52A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40790797 | |||||||
| chr4:40790908 | A | G | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1180+163A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40790908 | |||||||
| chr4:40791181 | C | T | 1 | a0001c0001t0019g0223 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1180+436C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791181 | |||||||
| chr4:40791214 | A | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1180+469A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791214 | |||||||
| chr4:40791432 | T | C | 1 | a0004c0004t0008g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1180+687T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791432 | |||||||
| chr4:40791614 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
139 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1180+869T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791614 | |||||||
| chr4:40791691 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1180+946C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791691 | |||||||
| chr4:40791743 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1180+998G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40791743 | |||||||
| chr4:40792039 | C | T | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1180+1294C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792039 | |||||||
| chr4:40792440 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+1695A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792440 | |||||||
| chr4:40792443 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(122): Show |
135 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1180+1698G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792443 | |||||||
| chr4:40792445 | A | G | 1 | a0002c0002t0001g0284 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1180+1700A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792445 | |||||||
| chr4:40792477 | A | C | 36 | a0001c0001t0001g0083 a0001c0001t0001g0229 a0001c0001t0002g0113 others(33): Show |
36 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1180+1732A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792477 | |||||||
| chr4:40792480 | G | C | 4 | a0003c0003t0006g0361 a0003c0003t0006g0362 a0003c0003t0021g0037 others(1): Show |
4 | HG00438.hp1 NA18947.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+1735G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792480 | |||||||
| chr4:40792489 | C | T | 1 | a0002c0002t0001g0235 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1180+1744C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792489 | |||||||
| chr4:40792517 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0007g0241 a0001c0001t0007g0245 others(3): Show |
6 | HG01952.hp1 NA18969.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+1772C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792517 | |||||||
| chr4:40792522 | A | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
212 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.1180+1777A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792522 | |||||||
| chr4:40792545 | C | A | 13 | a0001c0001t0001g0064 a0001c0001t0001g0179 a0001c0001t0001g0181 others(10): Show |
13 | HG01123.hp2 HG01928.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180+1800C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792545 | |||||||
| chr4:40792546 | T | C | 1 | a0013c0009t0007g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1180+1801T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792546 | |||||||
| chr4:40792547 | C | T | 1 | a0011c0021t0002g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1180+1802C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792547 | |||||||
| chr4:40792579 | G | A | 1 | a0002c0002t0001g0298 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1181-1796G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792579 | |||||||
| chr4:40792608 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-1767G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792608 | |||||||
| chr4:40792613 | A | C | 2 | a0003c0003t0015g0158 a0003c0003t0015g0240 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1181-1762A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792613 | |||||||
| chr4:40792637 | G | C | 3 | a0002c0002t0001g0019 a0002c0002t0001g0277 a0017c0011t0004g0358 |
4 | HG02015.hp1 NA18984.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-1738G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792637 | |||||||
| chr4:40792668 | T | C | 1 | a0003c0003t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1181-1707T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792668 | |||||||
| chr4:40792668 | T | G | 5 | a0001c0001t0039g0230 a0003c0003t0003g0340 a0003c0003t0003g0343 others(2): Show |
5 | HG01081.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181-1707T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792668 | |||||||
| chr4:40792679 | G | A | 22 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(19): Show |
22 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1181-1696G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792679 | |||||||
| chr4:40792689 | C | T | 1 | a0002c0002t0002g0306 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1181-1686C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792689 | |||||||
| chr4:40792707 | G | C | 13 | a0001c0001t0039g0230 a0001c0001t0045g0066 a0001c0001t0047g0074 others(10): Show |
13 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181-1668G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792707 | |||||||
| chr4:40792722 | A | G | 1 | a0002c0002t0001g0262 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1181-1653A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792722 | |||||||
| chr4:40792723 | G | C | 1 | a0003c0003t0011g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1181-1652G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792723 | |||||||
| chr4:40792731 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(206): Show |
219 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.1181-1644G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792731 | |||||||
| chr4:40792763 | A | AAAG | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(208): Show |
221 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.1181-1611_1181-160 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 40792763 | ||||||
| chr4:40792763 | A | G | 2 | a0001c0001t0012g0323 a0001c0001t0020g0324 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1181-1612A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40792763 | |||||||
| chr4:40793181 | C | G | 1 | a0002c0002t0001g0295 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1181-1194C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793181 | |||||||
| chr4:40793199 | T | C | 1 | a0002c0002t0001g0288 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1181-1176T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793199 | |||||||
| chr4:40793311 | G | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-1064G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793311 | |||||||
| chr4:40793415 | C | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1181-960C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793415 | |||||||
| chr4:40793441 | C | CA | 14 | a0001c0001t0039g0230 a0001c0001t0045g0066 a0001c0001t0047g0074 others(11): Show |
14 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1181-927dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 40793441 | ||||||
| chr4:40793523 | G | A | 1 | a0002c0002t0001g0289 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1181-852G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793523 | |||||||
| chr4:40793658 | T | C | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1181-717T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793658 | |||||||
| chr4:40793723 | A | G | 11 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(8): Show |
11 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1181-652A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793723 | |||||||
| chr4:40793730 | G | A | 3 | a0003c0003t0003g0217 a0003c0003t0003g0226 a0003c0022t0003g0346 |
3 | HG00140.hp1 HG03654.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1181-645G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793730 | |||||||
| chr4:40793761 | T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-614T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793761 | |||||||
| chr4:40793791 | T | C | 4 | a0001c0001t0002g0220 a0001c0001t0010g0225 a0001c0001t0019g0223 others(1): Show |
4 | HG02258.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181-584T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793791 | |||||||
| chr4:40793822 | T | C | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1181-553T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793822 | |||||||
| chr4:40793836 | A | G | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1181-539A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793836 | |||||||
| chr4:40793841 | T | C | 1 | a0003c0003t0006g0363 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1181-534T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793841 | |||||||
| chr4:40793868 | A | C | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1181-507A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40793868 | |||||||
| chr4:40794290 | A | C | 2 | a0001c0013t0002g0153 a0006c0007t0028g0043 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1181-85A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40794290 | |||||||
| chr4:40794346 | A | G | 1 | a0002c0002t0005g0359 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1181-29A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 8/11 | chr4 | 40794346 | |||||||
| chr4:40794542 | C | T | 6 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(3): Show |
6 | HG02559.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+66C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794542 | |||||||
| chr4:40794555 | T | C | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+79T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794555 | |||||||
| chr4:40794695 | G | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(25): Show |
30 | HG00558.hp1 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282+219G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794695 | |||||||
| chr4:40794830 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
210 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1282+354C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794830 | |||||||
| chr4:40794876 | G | C | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1282+400G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794876 | |||||||
| chr4:40794990 | C | T | 7 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282+514C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40794990 | |||||||
| chr4:40795235 | A | G | 1 | a0001c0001t0007g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1282+759A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795235 | |||||||
| chr4:40795350 | C | T | 5 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282+874C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795350 | |||||||
| chr4:40795478 | T | A | 1 | a0003c0003t0011g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1282+1002T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795478 | |||||||
| chr4:40795676 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(210): Show |
223 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1282+1200A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795676 | |||||||
| chr4:40795733 | C | T | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1282+1257C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795733 | |||||||
| chr4:40795734 | G | C | 1 | a0002c0002t0005g0316 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1282+1258G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795734 | |||||||
| chr4:40795744 | C | T | 1 | a0002c0002t0001g0294 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1282+1268C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795744 | |||||||
| chr4:40795792 | G | T | 5 | a0002c0002t0010g0097 a0002c0002t0010g0120 a0002c0002t0010g0136 others(2): Show |
5 | HG02486.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282+1316G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795792 | |||||||
| chr4:40795806 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1282+1330C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795806 | |||||||
| chr4:40795910 | T | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(210): Show |
223 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1282+1434T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40795910 | |||||||
| chr4:40796095 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(210): Show |
223 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1282+1619T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796095 | |||||||
| chr4:40796211 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(210): Show |
223 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1282+1735G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796211 | |||||||
| chr4:40796244 | C | T | 7 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282+1768C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796244 | |||||||
| chr4:40796399 | G | A | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1282+1923G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796399 | |||||||
| chr4:40796490 | A | C | 8 | a0001c0001t0009g0331 a0001c0001t0009g0332 a0001c0001t0009g0338 others(5): Show |
8 | HG00735.hp2 HG01123.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282+2014A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796490 | |||||||
| chr4:40796522 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282+2046C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796522 | |||||||
| chr4:40796640 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1283-2147A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796640 | |||||||
| chr4:40796680 | C | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1283-2107C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796680 | |||||||
| chr4:40796716 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1283-2071C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796716 | |||||||
| chr4:40796718 | G | A | 6 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(3): Show |
6 | HG02559.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1283-2069G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796718 | |||||||
| chr4:40796791 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0053 a0001c0001t0001g0058 others(1): Show |
4 | HG03490.hp1 HG03704.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283-1996C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796791 | |||||||
| chr4:40796988 | G | A | 3 | a0001c0001t0018g0025 a0001c0001t0018g0026 a0003c0003t0014g0167 |
3 | NA18983.hp2 NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1283-1799G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796988 | |||||||
| chr4:40796993 | T | C | 1 | a0003c0003t0003g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1283-1794T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796993 | |||||||
| chr4:40796999 | G | A | 1 | a0002c0002t0001g0265 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1283-1788G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40796999 | |||||||
| chr4:40797006 | A | G | 1 | a0011c0021t0002g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1283-1781A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797006 | |||||||
| chr4:40797026 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1283-1761G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797026 | |||||||
| chr4:40797082 | C | G | 1 | a0001c0001t0002g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1283-1705C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797082 | |||||||
| chr4:40797366 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1283-1421C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797366 | |||||||
| chr4:40797514 | C | T | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1283-1273C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797514 | |||||||
| chr4:40797821 | C | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): Show |
140 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1283-966C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797821 | |||||||
| chr4:40797833 | G | A | 1 | a0003c0003t0003g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1283-954G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797833 | |||||||
| chr4:40797838 | C | G | 26 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(23): Show |
26 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1283-949C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797838 | |||||||
| chr4:40797896 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1283-891A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40797896 | |||||||
| chr4:40798060 | T | C | 1 | a0015c0015t0040g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1283-727T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798060 | |||||||
| chr4:40798107 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1283-680C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798107 | |||||||
| chr4:40798112 | G | T | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1283-675G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798112 | |||||||
| chr4:40798128 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1283-659A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798128 | |||||||
| chr4:40798130 | A | G | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283-657A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798130 | |||||||
| chr4:40798170 | A | G | 12 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0003c0003t0014g0167 others(9): Show |
12 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1283-617A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798170 | |||||||
| chr4:40798492 | C | T | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1283-295C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 9/11 | chr4 | 40798492 | |||||||
| chr4:40799073 | C | CT | 28 | a0001c0001t0001g0330 a0002c0002t0001g0005 a0002c0002t0001g0254 others(25): Show |
29 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1400+198dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799073 | C | CTTTTTG | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(123): Show |
135 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1400+174_1400+175i others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799073 | C | CTTTTTGT | 66 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(63): Show |
67 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1400+174_1400+175i others(9): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799073 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0002g0018 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1400+189_1400+198d others(12): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799073 | CT | C | 8 | a0001c0001t0009g0331 a0001c0001t0012g0337 a0001c0001t0013g0327 others(5): Show |
8 | HG00735.hp2 HG02055.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1400+198delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799073 | CTT | C | 13 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(10): Show |
13 | HG01123.hp1 HG01192.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1400+197_1400+198d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799073 | CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0001g0300 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1400+181_1400+198d others(20): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799073 | ||||||
| chr4:40799074 | T | TTTTTG | 55 | a0001c0001t0001g0089 a0001c0001t0001g0138 a0001c0001t0001g0200 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1400+174_1400+175i others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799074 | ||||||
| chr4:40799081 | T | G | 2 | a0001c0001t0039g0230 a0001c0013t0002g0153 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1400+177T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799081 | |||||||
| chr4:40799084 | T | G | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1400+180T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799084 | |||||||
| chr4:40799087 | T | G | 1 | a0001c0001t0045g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1400+183T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799087 | |||||||
| chr4:40799088 | T | G | 1 | a0007c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1400+184T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799088 | |||||||
| chr4:40799090 | T | G | 1 | a0006c0007t0048g0236 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1400+186T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799090 | |||||||
| chr4:40799102 | T | A | 1 | a0002c0002t0004g0020 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1400+198T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799102 | |||||||
| chr4:40799120 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0002g0194 others(1): Show |
4 | HG00733.hp1 HG01175.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1400+216C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799120 | |||||||
| chr4:40799149 | C | A | 8 | a0004c0004t0008g0068 a0004c0004t0008g0069 a0004c0004t0008g0070 others(5): Show |
8 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1400+245C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799149 | |||||||
| chr4:40799242 | C | CGG | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1400+339_1400+340i others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799242 | ||||||
| chr4:40799243 | G | A | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1400+339G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799243 | |||||||
| chr4:40799496 | TA | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
159 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.1400+607delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40799496 | ||||||
| chr4:40799598 | A | G | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1400+694A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799598 | |||||||
| chr4:40799667 | T | A | 2 | a0003c0003t0006g0165 a0003c0003t0006g0363 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1400+763T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799667 | |||||||
| chr4:40799848 | C | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0138 a0016c0019t0002g0105 |
3 | NA18948.hp2 NA19002.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1400+944C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799848 | |||||||
| chr4:40799881 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+977G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40799881 | |||||||
| chr4:40800076 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1400+1172G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800076 | |||||||
| chr4:40800080 | T | C | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1400+1176T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800080 | |||||||
| chr4:40800102 | T | G | 16 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(13): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+1198T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800102 | |||||||
| chr4:40800175 | T | C | 44 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(41): Show |
44 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1400+1271T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800175 | |||||||
| chr4:40800199 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1400+1295C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800199 | |||||||
| chr4:40800486 | C | A | 60 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1400+1582C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800486 | |||||||
| chr4:40800603 | G | A | 5 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+1699G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800603 | |||||||
| chr4:40800620 | G | A | 18 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1400+1716G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800620 | |||||||
| chr4:40800889 | T | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+1985T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800889 | |||||||
| chr4:40800893 | C | T | 26 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(23): Show |
26 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1400+1989C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40800893 | |||||||
| chr4:40801061 | A | AAGGGAGG others(29): Show |
1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+2172_1400+217 others(40): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801061 | ||||||
| chr4:40801077 | G | A | 5 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+2173G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801077 | |||||||
| chr4:40801079 | G | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): Show |
140 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1400+2175G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801079 | |||||||
| chr4:40801081 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+2177G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801081 | |||||||
| chr4:40801186 | A | G | 16 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(13): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+2282A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801186 | |||||||
| chr4:40801353 | T | C | 16 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(13): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+2449T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801353 | |||||||
| chr4:40801409 | A | T | 8 | a0001c0001t0007g0241 a0001c0001t0007g0244 a0001c0001t0007g0245 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1400+2505A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801409 | |||||||
| chr4:40801611 | T | G | 1 | a0002c0002t0001g0294 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1400+2707T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801611 | |||||||
| chr4:40801623 | C | A | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1400+2719C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801623 | |||||||
| chr4:40801723 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1400+2819C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801723 | |||||||
| chr4:40801725 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(271): Show |
284 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1400+2821T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801725 | |||||||
| chr4:40801758 | G | A | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1400+2854G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801758 | |||||||
| chr4:40801759 | T | TGTG | 6 | a0001c0001t0001g0014 a0001c0001t0001g0154 a0001c0001t0001g0155 others(3): Show |
6 | HG01891.hp2 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1400+2865_1400+286 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801759 | ||||||
| chr4:40801795 | G | A | 1 | a0007c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1400+2891G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801795 | |||||||
| chr4:40801816 | T | C | 16 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(13): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1400+2912T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801816 | |||||||
| chr4:40801901 | C | CA | 7 | a0001c0001t0002g0196 a0001c0013t0002g0153 a0002c0002t0001g0260 others(4): Show |
7 | HG00621.hp2 HG02027.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1400+3015dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | ||||||
| chr4:40801901 | C | CAA | 19 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(16): Show |
19 | HG00735.hp2 HG01069.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1400+3014_1400+301 others(6): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | ||||||
| chr4:40801901 | C | CAAA | 22 | a0001c0001t0012g0323 a0003c0003t0003g0237 a0003c0003t0006g0049 others(19): Show |
22 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1400+3013_1400+301 others(7): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | ||||||
| chr4:40801901 | C | CAAAA | 17 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(14): Show |
17 | HG00438.hp1 HG00733.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1400+3012_1400+301 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | ||||||
| chr4:40801901 | CAAAAAA | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
156 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.1400+3010_1400+301 others(10): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40801901 | ||||||
| chr4:40801942 | G | A | 1 | a0007c0006t0015g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1400+3038G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801942 | |||||||
| chr4:40801962 | T | G | 28 | a0001c0001t0001g0229 a0001c0001t0002g0186 a0001c0001t0002g0187 others(25): Show |
28 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1400+3058T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40801962 | |||||||
| chr4:40802117 | A | G | 1 | a0001c0001t0012g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1400+3213A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802117 | |||||||
| chr4:40802338 | AT | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(58): Show |
61 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1400+3443delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802338 | ||||||
| chr4:40802340 | T | A | 3 | a0001c0001t0018g0025 a0001c0001t0018g0026 a0001c0001t0039g0230 |
3 | HG02976.hp2 NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1400+3436T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802340 | |||||||
| chr4:40802520 | A | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(131): Show |
144 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1400+3616A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802520 | |||||||
| chr4:40802575 | C | T | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+3671C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802575 | |||||||
| chr4:40802631 | A | ATGTT | 271 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(268): Show |
281 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.1400+3737_1400+374 others(8): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802631 | ||||||
| chr4:40802641 | G | GTTTGT | 5 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400+3740_1400+374 others(9): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802641 | ||||||
| chr4:40802645 | T | G | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1400+3741T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802645 | |||||||
| chr4:40802691 | A | T | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1400+3787A>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802691 | |||||||
| chr4:40802738 | A | G | 4 | a0003c0003t0006g0049 a0003c0003t0006g0059 a0003c0003t0006g0060 others(1): Show |
4 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1400+3834A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802738 | |||||||
| chr4:40802783 | C | CT | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(135): Show |
148 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.1400+3896dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802783 | ||||||
| chr4:40802783 | CT | C | 48 | a0001c0001t0001g0200 a0001c0001t0009g0193 a0001c0001t0009g0328 others(45): Show |
48 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1400+3896delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40802783 | ||||||
| chr4:40802793 | T | G | 2 | a0003c0003t0014g0167 a0007c0006t0034g0356 |
2 | NA18906.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1400+3889T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802793 | |||||||
| chr4:40802827 | T | C | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1400+3923T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802827 | |||||||
| chr4:40802841 | A | G | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1400+3937A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802841 | |||||||
| chr4:40802994 | T | A | 1 | a0003c0003t0006g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1401-4067T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40802994 | |||||||
| chr4:40803007 | A | G | 1 | a0002c0002t0001g0282 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1401-4054A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803007 | |||||||
| chr4:40803032 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(279): Show |
293 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.1401-4029T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803032 | |||||||
| chr4:40803117 | C | T | 1 | a0003c0003t0016g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1401-3944C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803117 | |||||||
| chr4:40803164 | A | G | 55 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0003c0003t0003g0028 others(52): Show |
55 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1401-3897A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803164 | |||||||
| chr4:40803235 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
161 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1401-3826C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803235 | |||||||
| chr4:40803402 | G | A | 19 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(16): Show |
19 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1401-3659G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803402 | |||||||
| chr4:40803422 | A | G | 7 | a0003c0003t0011g0159 a0003c0003t0011g0162 a0003c0003t0011g0163 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-3639A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803422 | |||||||
| chr4:40803472 | C | T | 1 | a0003c0003t0044g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1401-3589C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803472 | |||||||
| chr4:40803525 | C | A | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1401-3536C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803525 | |||||||
| chr4:40803547 | G | T | 10 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(7): Show |
10 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1401-3514G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803547 | |||||||
| chr4:40803603 | A | G | 44 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0030 others(41): Show |
44 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1401-3458A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803603 | |||||||
| chr4:40803705 | C | T | 7 | a0001c0001t0002g0184 a0001c0001t0002g0190 a0001c0001t0002g0191 others(4): Show |
7 | HG01070.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-3356C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803705 | |||||||
| chr4:40803742 | G | C | 1 | a0005c0005t0001g0291 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1401-3319G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803742 | |||||||
| chr4:40803747 | G | C | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1401-3314G>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803747 | |||||||
| chr4:40803775 | G | T | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1401-3286G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803775 | |||||||
| chr4:40803949 | C | G | 2 | a0001c0001t0018g0025 a0001c0001t0018g0026 |
2 | NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1401-3112C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803949 | |||||||
| chr4:40803993 | G | A | 4 | a0002c0002t0010g0120 a0002c0002t0010g0136 a0002c0002t0010g0145 others(1): Show |
4 | HG02486.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401-3068G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40803993 | |||||||
| chr4:40804137 | G | A | 1 | a0001c0001t0007g0245 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1401-2924G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804137 | |||||||
| chr4:40804208 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1401-2853G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804208 | |||||||
| chr4:40804268 | C | T | 1 | a0003c0003t0031g0031 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1401-2793C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804268 | |||||||
| chr4:40804313 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0122 a0001c0001t0001g0131 others(3): Show |
7 | HG00558.hp1 NA18946.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-2748G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804313 | |||||||
| chr4:40804387 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1401-2674C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804387 | |||||||
| chr4:40804438 | C | CA | 13 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0134 others(10): Show |
13 | HG02055.hp2 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1401-2608dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40804438 | ||||||
| chr4:40804438 | CA | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0041g0248 others(4): Show |
7 | HG01070.hp2 HG01168.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-2608delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 40804438 | ||||||
| chr4:40804539 | A | G | 1 | a0001c0001t0009g0331 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1401-2522A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804539 | |||||||
| chr4:40804670 | A | C | 1 | a0001c0001t0007g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1401-2391A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804670 | |||||||
| chr4:40804841 | T | G | 16 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(13): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1401-2220T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40804841 | |||||||
| chr4:40805001 | A | G | 9 | a0001c0001t0004g0243 a0001c0001t0007g0241 a0001c0001t0007g0242 others(6): Show |
9 | HG02280.hp1 HG02486.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1401-2060A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805001 | |||||||
| chr4:40805224 | T | A | 5 | a0003c0003t0015g0158 a0003c0003t0015g0240 a0003c0003t0016g0239 others(2): Show |
5 | HG02965.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1401-1837T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805224 | |||||||
| chr4:40805282 | G | A | 7 | a0001c0001t0002g0184 a0001c0001t0002g0190 a0001c0001t0002g0191 others(4): Show |
7 | HG01070.hp1 HG01074.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1401-1779G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805282 | |||||||
| chr4:40805401 | G | A | 1 | a0006c0007t0028g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1401-1660G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40805401 | |||||||
| chr4:40806120 | G | A | 1 | a0001c0001t0039g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1401-941G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806120 | |||||||
| chr4:40806148 | C | T | 1 | a0007c0006t0034g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1401-913C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806148 | |||||||
| chr4:40806247 | G | A | 60 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1401-814G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806247 | |||||||
| chr4:40806275 | G | A | 1 | a0003c0003t0014g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1401-786G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806275 | |||||||
| chr4:40806367 | A | G | 2 | a0001c0001t0004g0243 a0001c0001t0007g0242 |
2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1401-694A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806367 | |||||||
| chr4:40806707 | A | G | 1 | a0001c0013t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1401-354A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806707 | |||||||
| chr4:40806749 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
149 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1401-312A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806749 | |||||||
| chr4:40806761 | G | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(277): Show |
290 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1401-300G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806761 | |||||||
| chr4:40806762 | C | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(198): Show |
211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1401-299C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806762 | |||||||
| chr4:40806763 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1401-298C>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806763 | |||||||
| chr4:40806765 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1401-296T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806765 | |||||||
| chr4:40806861 | A | G | 1 | a0003c0003t0006g0363 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1401-200A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 10/11 | chr4 | 40806861 | |||||||
| chr4:40807190 | GA | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(126): Show |
139 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1524+14delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40807190 | ||||||
| chr4:40807211 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1524+27T>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807211 | |||||||
| chr4:40807287 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1524+103T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807287 | |||||||
| chr4:40807296 | A | C | 1 | a0005c0005t0001g0280 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1524+112A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807296 | |||||||
| chr4:40807350 | C | CT | 22 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(19): Show |
22 | HG00735.hp1 HG00735.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+182dupT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40807350 | ||||||
| chr4:40807350 | CT | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(196): Show |
209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1524+182delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40807350 | ||||||
| chr4:40807372 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(271): Show |
284 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1524+188A>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807372 | |||||||
| chr4:40807434 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1524+250C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807434 | |||||||
| chr4:40807628 | G | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1524+444G>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807628 | |||||||
| chr4:40807641 | C | T | 2 | a0001c0001t0012g0323 a0001c0001t0020g0324 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1524+457C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807641 | |||||||
| chr4:40807669 | C | T | 3 | a0001c0001t0018g0025 a0001c0001t0018g0026 a0001c0001t0039g0230 |
3 | HG02976.hp2 NA18983.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1524+485C>T | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807669 | |||||||
| chr4:40807678 | C | G | 10 | a0001c0001t0045g0066 a0001c0001t0047g0074 a0004c0004t0008g0068 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+494C>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807678 | |||||||
| chr4:40807746 | T | C | 1 | a0002c0002t0001g0294 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1525-561T>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807746 | |||||||
| chr4:40807779 | A | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(268): Show |
281 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.1525-528A>C | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807779 | |||||||
| chr4:40807991 | G | A | 16 | a0001c0001t0009g0193 a0001c0001t0009g0328 a0001c0001t0009g0329 others(13): Show |
16 | HG00735.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1525-316G>A | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40807991 | |||||||
| chr4:40808029 | C | CA | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(138): Show |
151 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1525-254dupA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808029 | ||||||
| chr4:40808029 | C | CAA | 32 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0053 others(29): Show |
33 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1525-255_1525-254d others(4): Show |
NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808029 | ||||||
| chr4:40808029 | CA | C | 51 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0200 others(48): Show |
51 | HG00621.hp2 HG00735.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1525-254delA | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808029 | ||||||
| chr4:40808109 | GT | G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(252): Show |
265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1525-188delT | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 40808109 | ||||||
| chr4:40808116 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1525-191T>G | NSUN7 | ENSG00000179299.17 | transcript | ENST00000381782.7 | protein_coding | 11/11 | chr4 | 40808116 |