Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 340527 |
|---|---|
| ensemblid | ENSG00000204131.11 |
| hgncid | 33737 |
| symbol | NHSL2 |
| name | NHS like 2 |
| refseq_nuc | NM_001013627.3 |
| refseq_prot | NP_001013649.2 |
| ensembl_nuc | ENST00000633930.2 |
| ensembl_prot | ENSP00000488668.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 71910845 |
| end | 72153286 |
| strand | + |
| ver | v1.2 |
| region | chrX:71910845-72153286 |
| region5000 | chrX:71905845-72158286 |
| regionname0 | NHSL2_chrX_71910845_72153286 |
| regionname5000 | NHSL2_chrX_71905845_72158286 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1225 | 134 | 41 | 17 | 59 | 5 | 12 | 39 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002 | 0/0 | 1225 | 26 | 14 | 1 | 3 | 0 | 8 | 3 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003 | 0/0 | 1225 | 12 | 0 | 0 | 12 | 0 | 0 | 11 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0004 | 0/0 | 1225 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0005 | 0/0 | 1225 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0006 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0007 | 0/0 | 1225 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0008 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0009 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0010 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0011 | 0/0 | 1117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0012 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3678 | 113 | 24 | 15 | 59 | 4 | 11 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0002 | 0/0 | 3678 | 26 | 14 | 1 | 3 | 0 | 8 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0003 | 0/0 | 3678 | 14 | 14 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0004 | 0/0 | 3678 | 12 | 0 | 0 | 12 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0005 | 0/0 | 3678 | 4 | 0 | 0 | 4 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0006 | 0/0 | 3678 | 4 | 0 | 4 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0007 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0008 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0009 | 0/0 | 3681 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0010 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0011 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0012 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0013 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0014 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0015 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0016 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0017 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0018 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0019 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| c0020 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9929 | 48 | 7 | 4 | 36 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0002 | 0/0 | 9950 | 17 | 13 | 0 | 0 | 0 | 4 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0003 | 0/0 | 9950 | 11 | 1 | 7 | 0 | 2 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0004 | 0/0 | 9929 | 6 | 0 | 0 | 3 | 0 | 3 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0005 | 0/0 | 9946 | 4 | 3 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0006 | 0/0 | 9929 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0007 | 0/0 | 9940 | 3 | 0 | 0 | 0 | 0 | 3 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0008 | 0/0 | 9929 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0009 | 0/0 | 9928 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0010 | 0/0 | 9930 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0011 | 0/0 | 9949 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0012 | 0/0 | 9958 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0013 | 0/0 | 9946 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0014 | 0/0 | 9948 | 2 | 0 | 0 | 0 | 1 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0015 | 0/0 | 9949 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0016 | 0/0 | 9952 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0017 | 0/0 | 9954 | 2 | 0 | 1 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0018 | 0/0 | 9952 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0019 | 0/0 | 9956 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0020 | 0/0 | 9931 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0021 | 0/0 | 9931 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0022 | 0/0 | 9931 | 2 | 1 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0023 | 0/0 | 9955 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0024 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0025 | 0/0 | 9929 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0026 | 0/0 | 9931 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0027 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0028 | 0/0 | 9933 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0029 | 0/0 | 9935 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0030 | 0/0 | 9948 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0031 | 0/0 | 9949 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0032 | 0/0 | 9961 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0033 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0034 | 0/0 | 9949 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0035 | 0/0 | 9962 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0036 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0037 | 0/0 | 9938 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0038 | 0/0 | 9936 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0039 | 0/0 | 9940 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0040 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0041 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0042 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0043 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0044 | 0/0 | 9944 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0045 | 0/0 | 9952 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0046 | 0/0 | 9956 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0047 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0048 | 0/0 | 9955 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0049 | 0/0 | 9952 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0050 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0051 | 0/0 | 9950 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0052 | 0/0 | 9949 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0053 | 0/0 | 9954 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0054 | 0/0 | 9962 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0055 | 0/0 | 9960 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0056 | 0/0 | 9960 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0057 | 0/0 | 9945 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0058 | 0/0 | 9953 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0059 | 0/0 | 9928 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0060 | 0/0 | 9948 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0061 | 0/0 | 9928 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0062 | 0/0 | 9929 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0063 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0064 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0065 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0066 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0067 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0068 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0069 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0070 | 0/0 | 9939 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0071 | 0/0 | 9928 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0072 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0073 | 0/0 | 9945 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0074 | 0/0 | 9930 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0075 | 0/0 | 9947 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0076 | 0/0 | 9954 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0077 | 0/0 | 9952 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0078 | 0/0 | 9952 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0079 | 0/0 | 9954 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0080 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0081 | 0/0 | 9928 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0082 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0083 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| t0084 | 0/0 | 9939 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3678 | 113 | 24 | 15 | 59 | 4 | 11 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003 | 0/0 | 3678 | 14 | 14 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0011 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0012 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0013 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0014 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0015 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0019 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0020 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002 | 0/0 | 3678 | 26 | 14 | 1 | 3 | 0 | 8 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004 | 0/0 | 3678 | 12 | 0 | 0 | 12 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0004c0005 | 0/0 | 3678 | 4 | 0 | 0 | 4 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0005c0006 | 0/0 | 3678 | 4 | 0 | 4 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0006c0007 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0007c0008 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0008c0017 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0009c0010 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0010c0016 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0011c0009 | 0/0 | 3681 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0012c0018 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13606 | 41 | 6 | 3 | 31 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0003 | 0/0 | 13627 | 6 | 1 | 4 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0004 | 0/0 | 13606 | 5 | 0 | 0 | 2 | 0 | 3 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0005 | 0/0 | 13623 | 3 | 2 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0009 | 0/0 | 13605 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0010 | 0/0 | 13607 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0014 | 0/0 | 13625 | 2 | 0 | 0 | 0 | 1 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0015 | 0/0 | 13626 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0016 | 0/0 | 13629 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0017 | 0/0 | 13631 | 2 | 0 | 1 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0018 | 0/0 | 13629 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0019 | 0/0 | 13633 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0020 | 0/0 | 13608 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0021 | 0/0 | 13608 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0022 | 0/0 | 13608 | 2 | 1 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0023 | 0/0 | 13632 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0024 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0025 | 0/0 | 13606 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0026 | 0/0 | 13608 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0027 | 0/0 | 13604 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0037 | 0/0 | 13615 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0038 | 0/0 | 13613 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0039 | 0/0 | 13617 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0041 | 0/0 | 13608 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0042 | 0/0 | 13608 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0044 | 0/0 | 13621 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0045 | 0/0 | 13629 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0046 | 0/0 | 13633 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0047 | 0/0 | 13631 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0048 | 0/0 | 13632 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0049 | 0/0 | 13629 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0050 | 0/0 | 13631 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0051 | 0/0 | 13627 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0055 | 0/0 | 13637 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0056 | 0/0 | 13637 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0057 | 0/0 | 13622 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0060 | 0/0 | 13625 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0062 | 0/0 | 13606 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0064 | 0/0 | 13608 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0065 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0066 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0067 | 0/0 | 13596 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0068 | 0/0 | 13602 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0069 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0072 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0073 | 0/0 | 13622 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0074 | 0/0 | 13607 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0080 | 0/0 | 13604 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0081 | 0/0 | 13605 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0001t0083 | 0/0 | 13602 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0011 | 0/0 | 13626 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0012 | 0/0 | 13635 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0028 | 0/0 | 13610 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0029 | 0/0 | 13612 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0030 | 0/0 | 13625 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0031 | 0/0 | 13626 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0033 | 0/0 | 13635 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0034 | 0/0 | 13626 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0035 | 0/0 | 13639 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0036 | 0/0 | 13634 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0070 | 0/0 | 13616 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0003t0084 | 0/0 | 13616 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0011t0003 | 0/0 | 13627 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0012t0003 | 0/0 | 13627 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0013t0003 | 0/0 | 13627 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0014t0040 | 0/0 | 13604 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0015t0032 | 0/0 | 13638 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0019t0054 | 0/0 | 13639 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0001c0020t0005 | 0/0 | 13623 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0002 | 0/0 | 13627 | 17 | 13 | 0 | 0 | 0 | 4 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0007 | 0/0 | 13617 | 3 | 0 | 0 | 0 | 0 | 3 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0013 | 0/0 | 13623 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0059 | 0/0 | 13605 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0076 | 0/0 | 13631 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0077 | 0/0 | 13629 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0078 | 0/0 | 13629 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0002c0002t0079 | 0/0 | 13631 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0001 | 0/0 | 13606 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0004 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0006 | 0/0 | 13606 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0008 | 0/0 | 13606 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0061 | 0/0 | 13605 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0063 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0003c0004t0071 | 0/0 | 13605 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0004c0005t0001 | 0/0 | 13606 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0004c0005t0043 | 0/0 | 13608 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0004c0005t0082 | 0/0 | 13606 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0005c0006t0003 | 0/0 | 13627 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0005c0006t0016 | 0/0 | 13629 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0005c0006t0058 | 0/0 | 13630 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0006c0007t0013 | 0/0 | 13623 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0007c0008t0001 | 0/0 | 13606 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0008c0017t0053 | 0/0 | 13631 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0009c0010t0052 | 0/0 | 13626 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0010c0016t0075 | 0/0 | 13624 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0011c0009t0001 | 0/0 | 13609 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| a0012c0018t0001 | 0/0 | 13606 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | copy fasta | chrX | 71905845 | 72158286 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0014g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0014g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0015g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0016g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0017g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0017g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0018g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0018g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0019g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0019g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0020g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0021g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0021g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0022g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0022g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0023g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0025g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0026g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0027g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0037g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0038g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0039g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0041g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0042g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0044g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0045g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0046g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0047g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0048g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0049g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0050g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0051g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0055g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0056g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0057g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0060g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0062g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0064g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0065g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0066g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0067g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0068g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0069g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0072g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0073g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0074g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0080g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0081g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0001t0083g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0011g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0028g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0029g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0030g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0031g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0033g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0034g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0035g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0036g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0070g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0003t0084g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0011t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0012t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0013t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0014t0040g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0015t0032g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0019t0054g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0001c0020t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0007g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0059g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0076g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0077g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0078g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0002c0002t0079g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0008g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0061g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0063g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0003c0004t0071g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0004c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0004c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0004c0005t0043g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0004c0005t0082g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0005c0006t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0005c0006t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0005c0006t0016g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0005c0006t0058g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0006c0007t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0007c0008t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0008c0017t0053g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0009c0010t0052g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0010c0016t0075g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0011c0009t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| a0012c0018t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0125 | EUR | GBR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0120 | EUR | FIN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | CHS | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00642 | hp1 | a0001 | c0001 | t0016 | g0175 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00673 | hp1 | a0003 | c0004 | t0008 | g0085 | EAS | CHS | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG00738 | hp1 | a0002 | c0002 | t0078 | g0069 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01069 | hp1 | a0001 | c0001 | t0017 | g0166 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01074 | hp1 | a0001 | c0013 | t0003 | g0122 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01099 | hp1 | a0001 | c0001 | t0044 | g0164 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01167 | hp1 | a0001 | c0001 | t0019 | g0161 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01169 | hp1 | a0001 | c0001 | t0019 | g0160 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01169 | hp2 | a0005 | c0006 | t0003 | g0180 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01192 | hp1 | a0001 | c0001 | t0026 | g0172 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01258 | hp1 | a0007 | c0008 | t0001 | g0110 | AMR | CLM | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01358 | hp1 | a0001 | c0014 | t0040 | g0167 | AMR | CLM | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01515 | hp1 | a0001 | c0001 | t0048 | g0168 | EUR | IBS | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01928 | hp1 | a0001 | c0001 | t0046 | g0123 | AMR | PEL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01934 | hp1 | a0005 | c0006 | t0058 | g0079 | AMR | PEL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01943 | hp1 | a0005 | c0006 | t0016 | g0078 | AMR | PEL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG01952 | hp1 | a0005 | c0006 | t0003 | g0179 | AMR | PEL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02027 | hp1 | a0001 | c0001 | t0020 | g0042 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02055 | hp1 | a0006 | c0007 | t0013 | g0090 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02129 | hp1 | a0001 | c0001 | t0081 | g0081 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02135 | hp1 | a0001 | c0001 | t0068 | g0130 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02155 | hp1 | a0001 | c0001 | t0041 | g0044 | EAS | CDX | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02257 | hp1 | a0010 | c0016 | t0075 | g0137 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02257 | hp2 | a0012 | c0018 | t0001 | g0147 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0096 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02280 | hp2 | a0001 | c0001 | t0073 | g0134 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02451 | hp1 | a0001 | c0001 | t0038 | g0158 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02451 | hp2 | a0001 | c0001 | t0055 | g0068 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02523 | hp2 | a0001 | c0001 | t0066 | g0046 | EAS | KHV | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0105 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02602 | hp1 | a0001 | c0011 | t0003 | g0013 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02615 | hp1 | a0001 | c0015 | t0032 | g0031 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02615 | hp2 | a0001 | c0003 | t0029 | g0149 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02630 | hp1 | a0009 | c0010 | t0052 | g0185 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02698 | hp1 | a0001 | c0001 | t0018 | g0132 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02717 | hp1 | a0008 | c0017 | t0053 | g0059 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0173 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0145 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02809 | hp2 | a0001 | c0003 | t0012 | g0058 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02818 | hp2 | a0001 | c0003 | t0033 | g0093 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02886 | hp1 | a0001 | c0003 | t0012 | g0057 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02886 | hp2 | a0002 | c0002 | t0013 | g0102 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02895 | hp1 | a0001 | c0003 | t0035 | g0133 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02896 | hp1 | a0001 | c0001 | t0023 | g0055 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02965 | hp1 | a0001 | c0003 | t0084 | g0150 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0056 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02970 | hp2 | a0001 | c0001 | t0074 | g0142 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0157 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02976 | hp2 | a0001 | c0003 | t0030 | g0152 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0141 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03130 | hp1 | a0001 | c0003 | t0011 | g0156 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03209 | hp1 | a0001 | c0001 | t0056 | g0092 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03225 | hp1 | a0001 | c0003 | t0028 | g0159 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0171 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03453 | hp2 | a0001 | c0001 | t0039 | g0151 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0135 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03490 | hp1 | a0001 | c0001 | t0025 | g0015 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03492 | hp1 | a0002 | c0002 | t0076 | g0075 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03540 | hp1 | a0001 | c0001 | t0051 | g0187 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03540 | hp2 | a0001 | c0001 | t0022 | g0052 | AFR | GWD | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03579 | hp1 | a0001 | c0020 | t0005 | g0012 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03654 | hp1 | a0002 | c0002 | t0007 | g0129 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03688 | hp1 | a0001 | c0001 | t0045 | g0174 | SAS | STU | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03710 | hp1 | a0002 | c0002 | t0007 | g0106 | SAS | PJL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03834 | hp1 | a0001 | c0001 | t0047 | g0117 | SAS | BEB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | BEB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03942 | hp1 | a0001 | c0001 | t0018 | g0076 | SAS | BEB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG04199 | hp1 | a0001 | c0001 | t0062 | g0036 | SAS | STU | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG04204 | hp1 | a0002 | c0002 | t0007 | g0077 | SAS | STU | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0124 | SAS | STU | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18612 | hp1 | a0001 | c0001 | t0080 | g0073 | EAS | CHB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18747 | hp1 | a0001 | c0001 | t0022 | g0127 | EAS | CHB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18940 | hp1 | a0002 | c0002 | t0059 | g0029 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18943 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0121 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18945 | hp1 | a0003 | c0004 | t0006 | g0083 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18952 | hp1 | a0001 | c0001 | t0021 | g0006 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18953 | hp1 | a0003 | c0004 | t0006 | g0082 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18959 | hp1 | a0001 | c0001 | t0050 | g0119 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18960 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18961 | hp1 | a0001 | c0001 | t0049 | g0019 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18965 | hp1 | a0001 | c0001 | t0027 | g0025 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18967 | hp1 | a0001 | c0001 | t0083 | g0113 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18977 | hp1 | a0011 | c0009 | t0001 | g0176 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18982 | hp1 | a0003 | c0004 | t0063 | g0063 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18984 | hp1 | a0001 | c0001 | t0009 | g0184 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18985 | hp1 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18986 | hp1 | a0003 | c0004 | t0071 | g0011 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18989 | hp1 | a0002 | c0002 | t0077 | g0183 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18994 | hp1 | a0001 | c0001 | t0020 | g0139 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18995 | hp1 | a0004 | c0005 | t0001 | g0088 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19007 | hp1 | a0001 | c0001 | t0064 | g0009 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19009 | hp1 | a0001 | c0001 | t0021 | g0007 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19012 | hp1 | a0003 | c0004 | t0001 | g0043 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19043 | hp1 | a0001 | c0003 | t0031 | g0140 | AFR | LWK | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19060 | hp1 | a0002 | c0002 | t0079 | g0165 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19062 | hp1 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19063 | hp1 | a0003 | c0004 | t0061 | g0136 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19065 | hp1 | a0001 | c0001 | t0042 | g0109 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19065 | hp2 | a0001 | c0001 | t0069 | g0048 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19068 | hp1 | a0001 | c0001 | t0072 | g0038 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19074 | hp2 | a0003 | c0004 | t0008 | g0071 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19079 | hp1 | a0003 | c0004 | t0004 | g0186 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19082 | hp1 | a0001 | c0001 | t0065 | g0163 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19083 | hp1 | a0004 | c0005 | t0043 | g0061 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19085 | hp1 | a0003 | c0004 | t0008 | g0003 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0084 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19088 | hp1 | a0004 | c0005 | t0082 | g0062 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19091 | hp1 | a0003 | c0004 | t0006 | g0112 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | YRI | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA19240 | hp2 | a0001 | c0001 | t0057 | g0103 | AFR | YRI | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20129 | hp1 | a0001 | c0001 | t0037 | g0154 | AFR | ASW | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20129 | hp2 | a0001 | c0003 | t0011 | g0155 | AFR | ASW | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | TSI | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20805 | hp1 | a0001 | c0012 | t0003 | g0169 | EUR | TSI | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | GIH | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0049 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02109 | hp2 | a0001 | c0001 | t0067 | g0148 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02559 | hp1 | a0001 | c0003 | t0034 | g0153 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG02559 | hp2 | a0001 | c0019 | t0054 | g0070 | AFR | ACB | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0101 | AFR | MSL | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG06807 | hp1 | a0001 | c0003 | t0070 | g0027 | AFR | USA | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| HG06807 | hp2 | a0001 | c0003 | t0036 | g0054 | AFR | USA | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA18955 | hp1 | a0004 | c0005 | t0001 | g0087 | EAS | JPT | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20300 | hp1 | a0001 | c0001 | t0060 | g0080 | AFR | USA | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | USA | NHSL2_chrX_71905845_72158286 | NHSL2 | chrX | 71905845 | 72158286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71911275
|
G | A | 1 | a0004 | 4 | NA18955.hp1 NA18995.hp1 NA19083.hp1 others(1): Show |
missense_variant | MODERATE | c.188G>A | p.Arg63His | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/8 | 431/13633 | 188/3678 | 63/1225 | chrX | 71911275 | ||
| chrX:72132104
|
T | G | 1 | a0006 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.306T>G | p.Asn102Lys | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/8 | 549/13633 | 306/3678 | 102/1225 | chrX | 72132104 | ||
| chrX:72132121
|
A | C | 1 | a0012 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.323A>C | p.His108Pro | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/8 | 566/13633 | 323/3678 | 108/1225 | chrX | 72132121 | ||
| chrX:72134136
|
C | A | 1 | a0007 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.482C>A | p.Thr161Asn | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 3/8 | 725/13633 | 482/3678 | 161/1225 | chrX | 72134136 | ||
| chrX:72134198
|
C | T | 1 | a0008 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.544C>T | p.Arg182Cys | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 3/8 | 787/13633 | 544/3678 | 182/1225 | chrX | 72134198 | ||
| chrX:72134530
|
G | A | 2 | a0003a0011 | 13 | HG00673.hp1 NA18944.hp1 NA18945.hp1 others(10): Show |
missense_variant | MODERATE | c.586G>A | p.Glu196Lys | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/8 | 829/13633 | 586/3678 | 196/1225 | chrX | 72134530 | ||
| chrX:72140042
|
C | T | 1 | a0005 | 4 | HG01169.hp2 HG01934.hp1 HG01943.hp1 others(1): Show |
missense_variant | MODERATE | c.2494C>T | p.Arg832Cys | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 2737/13633 | 2494/3678 | 832/1225 | chrX | 72140042 | ||
| chrX:72140250
|
C | T | 1 | a0002 | 26 | HG00738.hp1 HG02486.hp1 HG02572.hp1 others(23): Show |
missense_variant | MODERATE | c.2702C>T | p.Thr901Ile | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 2945/13633 | 2702/3678 | 901/1225 | chrX | 72140250 | ||
| chrX:72140282
|
C | T | 1 | a0010 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.2734C>T | p.His912Tyr | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 2977/13633 | 2734/3678 | 912/1225 | chrX | 72140282 | ||
| chrX:72140758
|
G | T | 1 | a0009 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.3210G>T | p.Glu1070Asp | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 3453/13633 | 3210/3678 | 1070/1225 | chrX | 72140758 | ||
| chrX:72142338
|
T | TGAAGA | 1 | a0011 | 1 | NA18977.hp1 | frameshift_variant | HIGH | c.3331_3335dupGAAGA | p.Asp1112fs | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/8 | 3579/13633 | 3336/3678 | 1112/1225 | INFO_REALIGN_3_PRIME | chrX | 72142338 | |
| chrX:72143256
|
CA | C | 1 | a0011 | 1 | NA18977.hp1 | frameshift_variant | HIGH | c.3364delA | p.Arg1122fs | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3607/13633 | 3364/3678 | 1122/1225 | INFO_REALIGN_3_PRIME | chrX | 72143256 | |
| chrX:72143300
|
TG | T | 1 | a0011 | 1 | NA18977.hp1 | frameshift_variant | HIGH | c.3407delG | p.Gly1136fs | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3650/13633 | 3407/3678 | 1136/1225 | INFO_REALIGN_3_PRIME | chrX | 72143300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71911225
|
C | T | 1 | a0001c0020 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.138C>T | p.His46His | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/8 | 381/13633 | 138/3678 | 46/1225 | chrX | 71911225 | ||
| chrX:72132098
|
G | T | 1 | a0001c0019 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.300G>T | p.Arg100Arg | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/8 | 543/13633 | 300/3678 | 100/1225 | chrX | 72132098 | ||
| chrX:72134595
|
C | T | 1 | a0010c0016 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.651C>T | p.Ala217Ala | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/8 | 894/13633 | 651/3678 | 217/1225 | chrX | 72134595 | ||
| chrX:72138994
|
G | A | 1 | a0009c0010 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1446G>A | p.Ser482Ser | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 1689/13633 | 1446/3678 | 482/1225 | chrX | 72138994 | ||
| chrX:72140128
|
C | T | 1 | a0001c0015 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.2580C>T | p.Phe860Phe | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 2823/13633 | 2580/3678 | 860/1225 | chrX | 72140128 | ||
| chrX:72140293
|
A | C | 1 | a0001c0014 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.2745A>C | p.Pro915Pro | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 2988/13633 | 2745/3678 | 915/1225 | chrX | 72140293 | ||
| chrX:72140335
|
C | T | 1 | a0001c0013 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.2787C>T | p.Pro929Pro | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 3030/13633 | 2787/3678 | 929/1225 | chrX | 72140335 | ||
| chrX:72140398
|
G | A | 1 | a0001c0011 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.2850G>A | p.Thr950Thr | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/8 | 3093/13633 | 2850/3678 | 950/1225 | chrX | 72140398 | ||
| chrX:72143463
|
A | C | 1 | a0001c0012 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.3567A>C | p.Pro1189Pro | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3810/13633 | 3567/3678 | 1189/1225 | chrX | 72143463 | ||
| chrX:72143565
|
C | T | 18 | a0001c0001a0001c0011a0001c0012others(15): Show | 172 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
synonymous_variant | LOW | c.3669C>T | p.Pro1223Pro | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3912/13633 | 3669/3678 | 1223/1225 | chrX | 72143565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71910924
|
C | G | 1 | a0001c0003t0084 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-164C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/8 | 164 | chrX | 71910924 | |||||
| chrX:72143639
|
T | TC | 1 | a0001c0001t0023 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 67 | INFO_REALIGN_3_PRIME | chrX | 72143639 | ||||
| chrX:72143825
|
TC | T | 1 | a0001c0001t0024 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*256delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 256 | INFO_REALIGN_3_PRIME | chrX | 72143825 | ||||
| chrX:72144014
|
G | A | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG01192.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*440G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 440 | chrX | 72144014 | |||||
| chrX:72144082
|
TC | T | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 512 | INFO_REALIGN_3_PRIME | chrX | 72144082 | ||||
| chrX:72144089
|
C | T | 1 | a0004c0005t0082 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 515 | chrX | 72144089 | |||||
| chrX:72144141
|
TG | T | 1 | a0001c0001t0027 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 569 | INFO_REALIGN_3_PRIME | chrX | 72144141 | ||||
| chrX:72144214
|
A | G | 46 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(43): Show | 119 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*640A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 640 | chrX | 72144214 | |||||
| chrX:72144233
|
G | GT | 1 | a0001c0001t0024 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*662dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 663 | INFO_REALIGN_3_PRIME | chrX | 72144233 | ||||
| chrX:72144253
|
G | GC | 2 | a0001c0001t0010a0005c0006t0058 | 4 | HG01934.hp1 NA18943.hp1 NA18979.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*686dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 687 | INFO_REALIGN_3_PRIME | chrX | 72144253 | ||||
| chrX:72144375
|
G | T | 1 | a0001c0001t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 801 | chrX | 72144375 | |||||
| chrX:72144472
|
TA | T | 2 | a0001c0001t0080a0001c0001t0081 | 2 | HG02129.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*902delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 902 | INFO_REALIGN_3_PRIME | chrX | 72144472 | ||||
| chrX:72144483
|
A | G | 1 | a0001c0001t0019 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*909A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 909 | chrX | 72144483 | |||||
| chrX:72144504
|
G | T | 4 | a0001c0001t0055a0001c0001t0056a0001c0019t0054others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*930G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 930 | chrX | 72144504 | |||||
| chrX:72144629
|
A | C | 86 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(83): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1055A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1055 | chrX | 72144629 | |||||
| chrX:72144692
|
A | G | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1118A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1118 | chrX | 72144692 | |||||
| chrX:72144704
|
G | GCA | 7 | a0001c0003t0011a0001c0003t0012a0001c0003t0033others(4): Show | 9 | HG00738.hp1 HG02559.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1171_*1172dupCA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1173 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
G | GCACA | 1 | a0001c0001t0019 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1169_*1172dupCACA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1173 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
G | GCACACAC others(1): Show |
1 | a0001c0003t0036 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165_*1172dupCACA others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1173 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCA | G | 5 | a0001c0001t0049a0001c0001t0050a0001c0003t0029others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1171_*1172delCA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1171 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCACA | G | 6 | a0001c0001t0018a0001c0001t0045a0001c0001t0046others(3): Show | 7 | HG01928.hp1 HG01934.hp1 HG02698.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1169_*1172delCACA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1169 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCACACA | G | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0014others(13): Show | 27 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1172delCACA others(2): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1167 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCACACAC others(1): Show |
G | 8 | a0001c0001t0021a0001c0001t0022a0001c0001t0055others(5): Show | 10 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1165_*1172delCACA others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1165 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCACACAC others(3): Show |
G | 39 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(36): Show | 96 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1163_*1172delCACA others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1163 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCACACAC others(5): Show |
G | 1 | a0002c0002t0059 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1161_*1172delCACA others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1161 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144704
|
GCACACAC others(7): Show |
G | 5 | a0001c0001t0037a0001c0001t0038a0001c0001t0039others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1172delCACA others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1159 | INFO_REALIGN_3_PRIME | chrX | 72144704 | ||||
| chrX:72144737
|
CACACACA others(2): Show |
C | 1 | a0001c0001t0074 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165_*1173delCACA others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1165 | INFO_REALIGN_3_PRIME | chrX | 72144737 | ||||
| chrX:72144741
|
CACACA | C | 1 | a0001c0001t0048 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169_*1173delCACA others(1): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1169 | INFO_REALIGN_3_PRIME | chrX | 72144741 | ||||
| chrX:72144866
|
C | T | 4 | a0001c0001t0055a0001c0001t0056a0001c0019t0054others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1292C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1292 | chrX | 72144866 | |||||
| chrX:72145023
|
A | C | 1 | a0001c0001t0019 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1449A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1449 | chrX | 72145023 | |||||
| chrX:72145225
|
G | A | 86 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(83): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1651G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1651 | chrX | 72145225 | |||||
| chrX:72145570
|
A | G | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 1996 | chrX | 72145570 | |||||
| chrX:72145745
|
T | C | 23 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(20): Show | 34 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2171T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2171 | chrX | 72145745 | |||||
| chrX:72145815
|
TC | T | 2 | a0001c0001t0027a0001c0001t0083 | 2 | NA18965.hp1 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2245delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2245 | INFO_REALIGN_3_PRIME | chrX | 72145815 | ||||
| chrX:72146012
|
C | A | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2438C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2438 | chrX | 72146012 | |||||
| chrX:72146102
|
A | G | 1 | a0001c0001t0019 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2528A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2528 | chrX | 72146102 | |||||
| chrX:72146164
|
AG | A | 1 | a0010c0016t0075 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2591delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2591 | chrX | 72146164 | |||||
| chrX:72146181
|
A | AG | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2608dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2609 | INFO_REALIGN_3_PRIME | chrX | 72146181 | ||||
| chrX:72146301
|
C | A | 86 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(83): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2727C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2727 | chrX | 72146301 | |||||
| chrX:72146307
|
A | T | 4 | a0001c0001t0055a0001c0001t0056a0001c0019t0054others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2733A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 2733 | chrX | 72146307 | |||||
| chrX:72146826
|
CCAGCCCC others(11): Show |
C | 2 | a0001c0003t0028a0001c0003t0029 | 2 | HG02615.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3267_*3284delTCCT others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3267 | INFO_REALIGN_3_PRIME | chrX | 72146826 | ||||
| chrX:72146929
|
G | A | 1 | a0001c0003t0033 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3355G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3355 | chrX | 72146929 | |||||
| chrX:72147309
|
G | A | 2 | a0003c0004t0006a0003c0004t0061 | 4 | NA18945.hp1 NA18953.hp1 NA19063.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3735G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3735 | chrX | 72147309 | |||||
| chrX:72147310
|
T | C | 93 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(90): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*3736T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3736 | chrX | 72147310 | |||||
| chrX:72147447
|
G | A | 1 | a0010c0016t0075 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3873G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3873 | chrX | 72147447 | |||||
| chrX:72147479
|
A | G | 1 | a0001c0003t0034 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3905A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 3905 | chrX | 72147479 | |||||
| chrX:72148007
|
C | T | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4433C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 4433 | chrX | 72148007 | |||||
| chrX:72148063
|
A | G | 2 | a0001c0001t0072a0001c0001t0083 | 2 | NA18967.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4489A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 4489 | chrX | 72148063 | |||||
| chrX:72148069
|
T | G | 1 | a0001c0001t0062 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 4495 | chrX | 72148069 | |||||
| chrX:72148094
|
T | A | 11 | a0001c0001t0005a0001c0001t0051a0001c0001t0073others(8): Show | 31 | HG00738.hp1 HG01109.hp1 HG02257.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4520T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 4520 | chrX | 72148094 | |||||
| chrX:72148494
|
G | A | 86 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(83): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*4920G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 4920 | chrX | 72148494 | |||||
| chrX:72148571
|
T | C | 1 | a0001c0001t0037 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4997T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 4997 | chrX | 72148571 | |||||
| chrX:72148610
|
T | C | 1 | a0003c0004t0063 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5036T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5036 | chrX | 72148610 | |||||
| chrX:72148734
|
T | C | 1 | a0002c0002t0076 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5160T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5160 | chrX | 72148734 | |||||
| chrX:72148820
|
AAG | A | 1 | a0001c0001t0044 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5261_*5262delAG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5261 | INFO_REALIGN_3_PRIME | chrX | 72148820 | ||||
| chrX:72148835
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0073 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5265_*5266insGTGT others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5266 | INFO_REALIGN_3_PRIME | chrX | 72148835 | ||||
| chrX:72148835
|
A | T | 1 | a0001c0001t0044 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5261A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5261 | chrX | 72148835 | |||||
| chrX:72148835
|
AGTGTAT | A | 2 | a0001c0001t0026a0001c0001t0064 | 2 | HG01192.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5266_*5271delATGT others(2): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5266 | INFO_REALIGN_3_PRIME | chrX | 72148835 | ||||
| chrX:72148835
|
AGTGTATG others(1): Show |
A | 40 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(37): Show | 97 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*5266_*5273delATGT others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5266 | INFO_REALIGN_3_PRIME | chrX | 72148835 | ||||
| chrX:72148838
|
G | A | 1 | a0001c0001t0044 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5264G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5264 | chrX | 72148838 | |||||
| chrX:72148840
|
A | ATG | 8 | a0001c0001t0014a0001c0001t0039a0001c0001t0049others(5): Show | 27 | HG00140.hp1 HG00738.hp1 HG02486.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5304_*5305dupGT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | ATGTG | 14 | a0001c0001t0003a0001c0001t0015a0001c0001t0018others(11): Show | 22 | HG01074.hp1 HG01106.hp1 HG01169.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5302_*5305dupGTGT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | ATGTGTG | 5 | a0001c0001t0016a0001c0001t0046a0001c0001t0047others(2): Show | 5 | HG00642.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5300_*5305dupGTGT others(2): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0005a0001c0001t0017a0001c0001t0023others(4): Show | 10 | HG00280.hp1 HG01069.hp1 HG01109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5298_*5305dupGTGT others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | ATGTGTGT others(3): Show |
2 | a0008c0017t0053a0010c0016t0075 | 2 | HG02257.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5296_*5305dupGTGT others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | ATGTGTGT others(11): Show |
2 | a0001c0001t0055a0001c0019t0054 | 2 | HG02451.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5288_*5305dupGTGT others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0056 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5286_*5305dupGTGT others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5306 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148840
|
A | G | 3 | a0001c0001t0019a0001c0001t0044a0001c0001t0073 | 4 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5266A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5266 | chrX | 72148840 | |||||
| chrX:72148840
|
ATG | A | 4 | a0001c0001t0038a0001c0003t0028a0001c0003t0029others(1): Show | 4 | HG02451.hp1 HG02615.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5304_*5305delGT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5304 | INFO_REALIGN_3_PRIME | chrX | 72148840 | ||||
| chrX:72148843
|
T | A | 2 | a0001c0001t0026a0001c0001t0064 | 2 | HG01192.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5269T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5269 | chrX | 72148843 | |||||
| chrX:72148845
|
T | A | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(38): Show | 98 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*5271T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5271 | chrX | 72148845 | |||||
| chrX:72148848
|
G | A | 1 | a0001c0001t0026 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5274G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5274 | chrX | 72148848 | |||||
| chrX:72148850
|
G | A | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(38): Show | 98 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*5276G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5276 | chrX | 72148850 | |||||
| chrX:72149119
|
A | G | 2 | a0001c0003t0028a0001c0003t0029 | 2 | HG02615.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5545A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5545 | chrX | 72149119 | |||||
| chrX:72149170
|
A | AAC | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5596_*5597insAC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5597 | chrX | 72149170 | |||||
| chrX:72149171
|
C | A | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5597C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5597 | chrX | 72149171 | |||||
| chrX:72149172
|
T | C | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5598T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5598 | chrX | 72149172 | |||||
| chrX:72149175
|
GCC | G | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5602_*5603delCC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5602 | chrX | 72149175 | |||||
| chrX:72149179
|
G | T | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5605G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5605 | chrX | 72149179 | |||||
| chrX:72149181
|
C | G | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5607C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5607 | chrX | 72149181 | |||||
| chrX:72149183
|
A | G | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5609A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5609 | chrX | 72149183 | |||||
| chrX:72149185
|
C | G | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5611C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5611 | chrX | 72149185 | |||||
| chrX:72149186
|
TG | T | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5614delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5614 | INFO_REALIGN_3_PRIME | chrX | 72149186 | ||||
| chrX:72149188
|
G | T | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5614G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5614 | chrX | 72149188 | |||||
| chrX:72149202
|
T | TA | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5642dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5643 | INFO_REALIGN_3_PRIME | chrX | 72149202 | ||||
| chrX:72149202
|
TA | T | 4 | a0001c0001t0009a0001c0001t0073a0003c0004t0061others(1): Show | 6 | HG02280.hp2 NA18960.hp1 NA18984.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5642delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5642 | INFO_REALIGN_3_PRIME | chrX | 72149202 | ||||
| chrX:72149501
|
A | G | 1 | a0001c0001t0045 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5927A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5927 | chrX | 72149501 | |||||
| chrX:72149532
|
G | A | 1 | a0001c0001t0065 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5958G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5958 | chrX | 72149532 | |||||
| chrX:72149548
|
A | G | 5 | a0001c0001t0037a0001c0001t0038a0001c0001t0039others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5974A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 5974 | chrX | 72149548 | |||||
| chrX:72149725
|
C | T | 85 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(82): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*6151C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 6151 | chrX | 72149725 | |||||
| chrX:72149752
|
G | C | 39 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(36): Show | 96 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*6178G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 6178 | chrX | 72149752 | |||||
| chrX:72149900
|
CTT | C | 1 | a0001c0014t0040 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6327_*6328delTT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 6327 | chrX | 72149900 | |||||
| chrX:72149954
|
G | T | 1 | a0001c0001t0069 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6380G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 6380 | chrX | 72149954 | |||||
| chrX:72150520
|
C | G | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6946C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 6946 | chrX | 72150520 | |||||
| chrX:72151026
|
C | CT | 8 | a0001c0001t0051a0002c0002t0002a0002c0002t0007others(5): Show | 26 | HG00738.hp1 HG02486.hp1 HG02572.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*7461dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 7462 | INFO_REALIGN_3_PRIME | chrX | 72151026 | ||||
| chrX:72151183
|
A | AT | 4 | a0001c0003t0028a0001c0003t0029a0001c0003t0030others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7623dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 7624 | INFO_REALIGN_3_PRIME | chrX | 72151183 | ||||
| chrX:72151183
|
AT | A | 4 | a0001c0001t0015a0001c0001t0057a0001c0001t0080others(1): Show | 5 | HG02109.hp1 HG02630.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7623delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 7623 | INFO_REALIGN_3_PRIME | chrX | 72151183 | ||||
| chrX:72151275
|
C | T | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7701C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 7701 | chrX | 72151275 | |||||
| chrX:72151545
|
A | C | 4 | a0001c0001t0005a0001c0001t0073a0001c0020t0005others(1): Show | 6 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7971A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 7971 | chrX | 72151545 | |||||
| chrX:72151750
|
C | CCCACCCT others(3): Show |
2 | a0001c0003t0070a0001c0003t0084 | 2 | HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8185_*8194dupGTCC others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8195 | INFO_REALIGN_3_PRIME | chrX | 72151750 | ||||
| chrX:72151807
|
T | C | 85 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(82): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*8233T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8233 | chrX | 72151807 | |||||
| chrX:72151874
|
G | A | 85 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(82): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*8300G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8300 | chrX | 72151874 | |||||
| chrX:72151959
|
G | A | 1 | a0001c0001t0041 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8385G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8385 | chrX | 72151959 | |||||
| chrX:72152196
|
G | A | 5 | a0001c0001t0037a0001c0001t0038a0001c0001t0039others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8622G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8622 | chrX | 72152196 | |||||
| chrX:72152295
|
A | G | 1 | a0008c0017t0053 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8721A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8721 | chrX | 72152295 | |||||
| chrX:72152339
|
G | A | 1 | a0001c0001t0066 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8765G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8765 | chrX | 72152339 | |||||
| chrX:72152340
|
T | C | 86 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(83): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*8766T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8766 | chrX | 72152340 | |||||
| chrX:72152348
|
TGCGCGC | T | 2 | a0001c0001t0046a0001c0001t0060 | 2 | HG01928.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8779_*8784delGCGC others(2): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8779 | INFO_REALIGN_3_PRIME | chrX | 72152348 | ||||
| chrX:72152351
|
GCGCGCGC others(1): Show |
G | 28 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(25): Show | 39 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*8779_*8786delGCGC others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8779 | INFO_REALIGN_3_PRIME | chrX | 72152351 | ||||
| chrX:72152351
|
GCGCGCGC others(3): Show |
G | 1 | a0001c0001t0055 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8779_*8788delGCGC others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8779 | INFO_REALIGN_3_PRIME | chrX | 72152351 | ||||
| chrX:72152351
|
GCGCGCGC others(5): Show |
G | 1 | a0001c0001t0056 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8779_*8790delGCGC others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8779 | INFO_REALIGN_3_PRIME | chrX | 72152351 | ||||
| chrX:72152353
|
GCGCGCA | G | 3 | a0001c0001t0020a0001c0001t0041a0001c0001t0042 | 4 | HG02027.hp1 HG02155.hp1 NA18994.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8781_*8786delGCGC others(2): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8781 | INFO_REALIGN_3_PRIME | chrX | 72152353 | ||||
| chrX:72152353
|
GCGCGCAC others(1): Show |
G | 48 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(45): Show | 124 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*8781_*8788delGCGC others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8781 | INFO_REALIGN_3_PRIME | chrX | 72152353 | ||||
| chrX:72152353
|
GCGCGCAC others(3): Show |
G | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8781_*8790delGCGC others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8781 | INFO_REALIGN_3_PRIME | chrX | 72152353 | ||||
| chrX:72152353
|
GCGCGCAC others(5): Show |
G | 1 | a0001c0001t0068 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8781_*8792delGCGC others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8781 | INFO_REALIGN_3_PRIME | chrX | 72152353 | ||||
| chrX:72152357
|
G | GCACA | 1 | a0001c0015t0032 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8814_*8817dupCACA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8818 | INFO_REALIGN_3_PRIME | chrX | 72152357 | ||||
| chrX:72152357
|
GCA | G | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8816_*8817delCA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8816 | INFO_REALIGN_3_PRIME | chrX | 72152357 | ||||
| chrX:72152357
|
GCACACAC others(1): Show |
G | 5 | a0001c0003t0011a0001c0003t0030a0001c0003t0031others(2): Show | 6 | HG02559.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8810_*8817delCACA others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8810 | INFO_REALIGN_3_PRIME | chrX | 72152357 | ||||
| chrX:72152363
|
A | G | 4 | a0001c0001t0020a0001c0001t0042a0001c0001t0046others(1): Show | 5 | HG01928.hp1 HG02027.hp1 NA18994.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8789A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8789 | chrX | 72152363 | |||||
| chrX:72152365
|
A | G | 76 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(73): Show | 163 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*8791A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8791 | chrX | 72152365 | |||||
| chrX:72152367
|
A | G | 2 | a0001c0001t0055a0001c0001t0083 | 2 | HG02451.hp2 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8793A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8793 | chrX | 72152367 | |||||
| chrX:72152369
|
A | G | 2 | a0001c0001t0056a0001c0001t0068 | 2 | HG02135.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8795A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8795 | chrX | 72152369 | |||||
| chrX:72152418
|
T | TTTAGG | 32 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(29): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*8846_*8850dupTAGG others(1): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8851 | INFO_REALIGN_3_PRIME | chrX | 72152418 | ||||
| chrX:72152476
|
T | A | 1 | a0001c0001t0021 | 2 | NA18952.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8902T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8902 | chrX | 72152476 | |||||
| chrX:72152481
|
C | T | 1 | a0001c0001t0019 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8907C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 8907 | chrX | 72152481 | |||||
| chrX:72152793
|
GA | G | 1 | a0001c0001t0083 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9221delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9221 | INFO_REALIGN_3_PRIME | chrX | 72152793 | ||||
| chrX:72152891
|
C | A | 88 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(85): Show | 177 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*9317C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9317 | chrX | 72152891 | |||||
| chrX:72153039
|
G | A | 1 | a0009c0010t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9465G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9465 | chrX | 72153039 | |||||
| chrX:72153060
|
CAAG | C | 4 | a0001c0001t0005a0001c0001t0073a0001c0020t0005others(1): Show | 6 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9493_*9495delAAG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9493 | INFO_REALIGN_3_PRIME | chrX | 72153060 | ||||
| chrX:72153159
|
TTTTTCTT others(3): Show |
T | 1 | a0001c0001t0067 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9589_*9598delTCTT others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9589 | INFO_REALIGN_3_PRIME | chrX | 72153159 | ||||
| chrX:72153176
|
T | TA | 2 | a0001c0003t0031a0001c0003t0036 | 2 | HG06807.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9613dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9614 | INFO_REALIGN_3_PRIME | chrX | 72153176 | ||||
| chrX:72153176
|
TA | T | 88 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(85): Show | 177 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*9613delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9613 | INFO_REALIGN_3_PRIME | chrX | 72153176 | ||||
| chrX:72153242
|
G | A | 5 | a0003c0004t0006a0003c0004t0008a0003c0004t0061others(2): Show | 9 | HG00673.hp1 NA18945.hp1 NA18953.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9668G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 8/8 | 9668 | chrX | 72153242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71911449
|
A | AC | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+85dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71911449 | |||||
| chrX:71911524
|
C | G | 1 | a0001c0001t0051g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280+157C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71911524 | ||||||
| chrX:71911598
|
C | G | 1 | a0003c0004t0004g0186 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.280+231C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71911598 | ||||||
| chrX:71911634
|
C | T | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+267C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71911634 | ||||||
| chrX:71911711
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(6): Show | 9 | HG00438.hp1 NA18943.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+344C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71911711 | ||||||
| chrX:71911844
|
A | G | 23 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0177others(20): Show | 23 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.280+477A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71911844 | ||||||
| chrX:71911921
|
G | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(15): Show | 18 | HG02132.hp1 HG02523.hp1 HG02602.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+554G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71911921 | ||||||
| chrX:71912012
|
C | G | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+645C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912012 | ||||||
| chrX:71912025
|
A | AC | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+663dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71912025 | |||||
| chrX:71912075
|
C | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+708C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912075 | ||||||
| chrX:71912428
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+1061G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912428 | ||||||
| chrX:71912633
|
A | C | 3 | a0001c0003t0011g0155a0001c0003t0011g0156a0002c0002t0002g0157 | 3 | HG02976.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280+1266A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912633 | ||||||
| chrX:71912745
|
C | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+1378C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912745 | ||||||
| chrX:71912799
|
GT | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.280+1436delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71912799 | |||||
| chrX:71912913
|
T | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(173): Show | 176 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.280+1546T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912913 | ||||||
| chrX:71912918
|
G | A | 1 | a0001c0001t0044g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.280+1551G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71912918 | ||||||
| chrX:71913553
|
C | T | 7 | a0001c0001t0003g0144a0001c0001t0005g0146a0001c0001t0074g0142others(4): Show | 7 | HG02258.hp1 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.280+2186C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71913553 | ||||||
| chrX:71913567
|
G | A | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+2200G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71913567 | ||||||
| chrX:71913585
|
A | AT | 1 | a0001c0001t0020g0139 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280+2219dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71913585 | |||||
| chrX:71913829
|
A | AG | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(174): Show | 177 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.280+2466dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71913829 | |||||
| chrX:71913960
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+2593T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71913960 | ||||||
| chrX:71914006
|
G | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+2639G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71914006 | ||||||
| chrX:71914056
|
T | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+2689T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71914056 | ||||||
| chrX:71914248
|
T | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+2881T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71914248 | ||||||
| chrX:71914585
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+3218G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71914585 | ||||||
| chrX:71914947
|
C | T | 3 | a0001c0001t0001g0138a0009c0010t0052g0185a0010c0016t0075g0137 | 3 | HG02257.hp1 HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+3580C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71914947 | ||||||
| chrX:71915073
|
TG | T | 1 | a0003c0004t0061g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.280+3708delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71915073 | |||||
| chrX:71915255
|
TG | T | 1 | a0003c0004t0061g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.280+3890delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71915255 | |||||
| chrX:71915448
|
G | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG02015.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+4081G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71915448 | ||||||
| chrX:71915662
|
T | C | 14 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0003g0050others(11): Show | 14 | HG01243.hp1 HG02109.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+4295T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71915662 | ||||||
| chrX:71916089
|
C | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+4722C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71916089 | ||||||
| chrX:71916232
|
G | A | 1 | a0001c0001t0015g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.280+4865G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71916232 | ||||||
| chrX:71916372
|
G | A | 1 | a0002c0002t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.280+5005G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71916372 | ||||||
| chrX:71916391
|
G | C | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+5024G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71916391 | ||||||
| chrX:71916525
|
C | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+5158C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71916525 | ||||||
| chrX:71916710
|
A | G | 1 | a0001c0001t0009g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.280+5343A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71916710 | ||||||
| chrX:71917018
|
A | G | 1 | a0001c0001t0069g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.280+5651A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917018 | ||||||
| chrX:71917146
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+5779G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917146 | ||||||
| chrX:71917252
|
T | TC | 1 | a0003c0004t0061g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.280+5888dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71917252 | |||||
| chrX:71917256
|
T | TC | 3 | a0001c0001t0009g0184a0002c0002t0079g0165a0004c0005t0043g0061 | 3 | NA18984.hp1 NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.280+5895dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71917256 | |||||
| chrX:71917259
|
C | CCCCT | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+5915_280+5918d others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71917259 | |||||
| chrX:71917259
|
CCCCT | C | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.280+5915_280+5918d others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71917259 | |||||
| chrX:71917280
|
C | G | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+5913C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917280 | ||||||
| chrX:71917494
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.280+6127C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917494 | ||||||
| chrX:71917495
|
T | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.280+6128T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917495 | ||||||
| chrX:71917558
|
A | G | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.280+6191A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917558 | ||||||
| chrX:71917587
|
A | T | 12 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(9): Show | 12 | HG02109.hp1 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+6220A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917587 | ||||||
| chrX:71917709
|
G | T | 1 | a0001c0001t0001g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.280+6342G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71917709 | ||||||
| chrX:71918022
|
A | G | 1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280+6655A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918022 | ||||||
| chrX:71918358
|
G | GA | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+6993dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71918358 | |||||
| chrX:71918360
|
A | AT | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+7009dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71918360 | |||||
| chrX:71918375
|
TTA | T | 3 | a0002c0002t0002g0064a0003c0004t0063g0063a0004c0005t0082g0062 | 3 | HG03239.hp1 NA18982.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.280+7009_280+7010d others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918375 | ||||||
| chrX:71918376
|
T | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+7009T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918376 | ||||||
| chrX:71918376
|
TA | T | 52 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0065others(49): Show | 52 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.280+7013delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71918376 | |||||
| chrX:71918377
|
A | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.280+7010A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918377 | ||||||
| chrX:71918378
|
A | T | 1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280+7011A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918378 | ||||||
| chrX:71918456
|
G | T | 85 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(82): Show | 85 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.280+7089G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918456 | ||||||
| chrX:71918643
|
C | T | 5 | a0001c0001t0003g0144a0001c0001t0005g0146a0001c0001t0074g0142others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+7276C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918643 | ||||||
| chrX:71918800
|
G | A | 85 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(82): Show | 85 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.280+7433G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71918800 | ||||||
| chrX:71919122
|
C | T | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+7755C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71919122 | ||||||
| chrX:71919301
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+7934A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71919301 | ||||||
| chrX:71919812
|
G | A | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+8445G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71919812 | ||||||
| chrX:71919861
|
G | T | 3 | a0001c0001t0001g0138a0009c0010t0052g0185a0010c0016t0075g0137 | 3 | HG02257.hp1 HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+8494G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71919861 | ||||||
| chrX:71919875
|
T | C | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+8508T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71919875 | ||||||
| chrX:71919915
|
A | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+8548A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71919915 | ||||||
| chrX:71920060
|
G | A | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+8693G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920060 | ||||||
| chrX:71920355
|
G | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(174): Show | 177 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.280+8988G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920355 | ||||||
| chrX:71920472
|
TA | T | 1 | a0001c0001t0004g0131 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.280+9118delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71920472 | |||||
| chrX:71920586
|
C | T | 39 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(36): Show | 39 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.280+9219C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920586 | ||||||
| chrX:71920735
|
C | CA | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+9377dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71920735 | |||||
| chrX:71920814
|
G | GT | 52 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0072others(49): Show | 52 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(49): Show |
intron_variant | MODIFIER | c.280+9455dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71920814 | |||||
| chrX:71920894
|
C | G | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+9527C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920894 | ||||||
| chrX:71920938
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.280+9571G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920938 | ||||||
| chrX:71920950
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+9583A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920950 | ||||||
| chrX:71920965
|
C | T | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+9598C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71920965 | ||||||
| chrX:71920971
|
AT | A | 1 | a0001c0001t0017g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.280+9609delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71920971 | |||||
| chrX:71921398
|
T | C | 1 | a0001c0014t0040g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.280+10031T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71921398 | ||||||
| chrX:71921399
|
G | A | 1 | a0001c0014t0040g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.280+10032G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71921399 | ||||||
| chrX:71921503
|
A | G | 2 | a0004c0005t0001g0087a0004c0005t0001g0088 | 2 | NA18955.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.280+10136A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71921503 | ||||||
| chrX:71921849
|
CTG | C | 1 | a0001c0001t0004g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.280+10485_280+1048 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71921849 | |||||
| chrX:71921858
|
C | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(31): Show | 34 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.280+10491C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71921858 | ||||||
| chrX:71921877
|
C | G | 1 | a0001c0001t0020g0139 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280+10510C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71921877 | ||||||
| chrX:71922248
|
G | T | 1 | a0001c0001t0068g0130 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.280+10881G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922248 | ||||||
| chrX:71922355
|
C | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+10988C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922355 | ||||||
| chrX:71922359
|
GA | G | 1 | a0001c0001t0005g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280+10995delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71922359 | |||||
| chrX:71922365
|
C | T | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.280+10998C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922365 | ||||||
| chrX:71922687
|
A | G | 2 | a0001c0001t0004g0128a0002c0002t0007g0129 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.280+11320A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922687 | ||||||
| chrX:71922785
|
T | A | 49 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0072others(46): Show | 49 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(46): Show |
intron_variant | MODIFIER | c.280+11418T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922785 | ||||||
| chrX:71922807
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.280+11440C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922807 | ||||||
| chrX:71922956
|
T | C | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280+11589T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71922956 | ||||||
| chrX:71923041
|
T | C | 1 | a0002c0002t0002g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.280+11674T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71923041 | ||||||
| chrX:71923047
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.280+11680A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71923047 | ||||||
| chrX:71923546
|
C | G | 1 | a0001c0001t0022g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.280+12179C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71923546 | ||||||
| chrX:71923575
|
C | A | 2 | a0001c0001t0001g0053a0001c0001t0015g0049 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.280+12208C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71923575 | ||||||
| chrX:71923742
|
C | T | 1 | a0008c0017t0053g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.280+12375C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71923742 | ||||||
| chrX:71924014
|
T | C | 2 | a0001c0001t0069g0048a0002c0002t0059g0029 | 2 | NA18940.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.280+12647T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71924014 | ||||||
| chrX:71924255
|
A | G | 112 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.280+12888A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71924255 | ||||||
| chrX:71924657
|
C | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(31): Show | 34 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.280+13290C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71924657 | ||||||
| chrX:71924928
|
C | G | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+13561C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71924928 | ||||||
| chrX:71925420
|
C | CT | 1 | a0003c0004t0061g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.280+14069dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71925420 | |||||
| chrX:71925420
|
CT | C | 4 | a0001c0001t0019g0160a0001c0001t0019g0161a0001c0001t0037g0154others(1): Show | 4 | HG01167.hp1 HG01169.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+14069delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71925420 | |||||
| chrX:71925626
|
T | C | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+14259T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71925626 | ||||||
| chrX:71926008
|
G | A | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+14641G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71926008 | ||||||
| chrX:71926150
|
TG | T | 2 | a0001c0001t0037g0154a0001c0001t0051g0187 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+14784delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71926150 | ||||||
| chrX:71926374
|
A | G | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+15007A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71926374 | ||||||
| chrX:71926625
|
A | AAT | 5 | a0001c0001t0001g0126a0001c0001t0014g0125a0001c0001t0038g0158others(2): Show | 5 | HG00140.hp1 HG02451.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+15262_280+1526 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71926625 | |||||
| chrX:71926625
|
A | AATAT | 1 | a0001c0001t0005g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280+15260_280+1526 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71926625 | |||||
| chrX:71926631
|
C | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(170): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.280+15264C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71926631 | ||||||
| chrX:71926740
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0080g0073others(3): Show | 6 | NA18612.hp1 NA18971.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+15373G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71926740 | ||||||
| chrX:71927192
|
C | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+15825C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71927192 | ||||||
| chrX:71927549
|
C | CT | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+16194dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71927549 | |||||
| chrX:71927549
|
CT | C | 5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(2): Show | 5 | HG02071.hp1 HG03239.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+16194delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71927549 | |||||
| chrX:71927549
|
CTTTT | C | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.280+16191_280+1619 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71927549 | |||||
| chrX:71927701
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+16334G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71927701 | ||||||
| chrX:71927828
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+16461G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71927828 | ||||||
| chrX:71928091
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0009g0184others(3): Show | 6 | NA18965.hp1 NA18984.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+16724A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71928091 | ||||||
| chrX:71928151
|
G | A | 1 | a0004c0005t0001g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.280+16784G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71928151 | ||||||
| chrX:71928409
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.280+17042A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71928409 | ||||||
| chrX:71929222
|
T | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(173): Show | 176 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.280+17855T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71929222 | ||||||
| chrX:71929238
|
T | G | 6 | a0001c0001t0057g0103a0002c0002t0002g0086a0002c0002t0002g0101others(3): Show | 6 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+17871T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71929238 | ||||||
| chrX:71929582
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+18215G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71929582 | ||||||
| chrX:71929646
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+18279T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71929646 | ||||||
| chrX:71929748
|
C | CT | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+18391dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71929748 | |||||
| chrX:71930213
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.280+18846C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71930213 | ||||||
| chrX:71930214
|
G | A | 1 | a0004c0005t0082g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.280+18847G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71930214 | ||||||
| chrX:71930406
|
A | G | 1 | a0001c0001t0010g0002 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.280+19039A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71930406 | ||||||
| chrX:71930628
|
A | G | 2 | a0001c0001t0001g0094a0002c0002t0002g0095 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.280+19261A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71930628 | ||||||
| chrX:71930699
|
C | T | 1 | a0001c0003t0033g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.280+19332C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71930699 | ||||||
| chrX:71931019
|
A | G | 1 | a0001c0001t0022g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280+19652A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71931019 | ||||||
| chrX:71931256
|
G | A | 3 | a0001c0001t0001g0138a0009c0010t0052g0185a0012c0018t0001g0147 | 3 | HG02257.hp2 HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+19889G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71931256 | ||||||
| chrX:71931270
|
G | C | 1 | a0001c0001t0051g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280+19903G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71931270 | ||||||
| chrX:71931520
|
T | C | 13 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(10): Show | 13 | HG02109.hp1 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.280+20153T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71931520 | ||||||
| chrX:71932013
|
A | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(11): Show | 14 | HG02132.hp1 HG02523.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.280+20646A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71932013 | ||||||
| chrX:71933117
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.280+21750G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71933117 | ||||||
| chrX:71933384
|
CT | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0072others(26): Show | 29 | HG01934.hp1 HG01943.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+22031delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71933384 | |||||
| chrX:71933843
|
G | C | 2 | a0001c0001t0037g0154a0001c0001t0051g0187 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+22476G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71933843 | ||||||
| chrX:71934363
|
A | G | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+22996A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71934363 | ||||||
| chrX:71934401
|
C | T | 1 | a0002c0002t0002g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280+23034C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71934401 | ||||||
| chrX:71934426
|
G | A | 1 | a0001c0001t0004g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280+23059G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71934426 | ||||||
| chrX:71935003
|
G | A | 13 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(10): Show | 13 | HG02109.hp1 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.280+23636G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71935003 | ||||||
| chrX:71935212
|
T | G | 2 | a0001c0001t0014g0125a0002c0002t0002g0124 | 2 | HG00140.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.280+23845T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71935212 | ||||||
| chrX:71935438
|
C | A | 6 | a0001c0001t0057g0103a0002c0002t0002g0086a0002c0002t0002g0101others(3): Show | 6 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+24071C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71935438 | ||||||
| chrX:71935680
|
TG | T | 1 | a0001c0001t0001g0182 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.280+24315delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71935680 | |||||
| chrX:71935850
|
G | A | 90 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.280+24483G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71935850 | ||||||
| chrX:71936040
|
G | A | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+24673G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71936040 | ||||||
| chrX:71936388
|
TC | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+25024delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71936388 | |||||
| chrX:71936393
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.280+25026T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71936393 | ||||||
| chrX:71936752
|
G | A | 90 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.280+25385G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71936752 | ||||||
| chrX:71936823
|
T | C | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+25456T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71936823 | ||||||
| chrX:71937314
|
G | T | 1 | a0001c0001t0046g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.280+25947G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71937314 | ||||||
| chrX:71937478
|
A | T | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(171): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.280+26111A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71937478 | ||||||
| chrX:71937490
|
C | T | 1 | a0001c0013t0003g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.280+26123C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71937490 | ||||||
| chrX:71937882
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.280+26515G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71937882 | ||||||
| chrX:71937892
|
G | C | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+26525G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71937892 | ||||||
| chrX:71938096
|
G | A | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+26729G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71938096 | ||||||
| chrX:71938435
|
A | T | 1 | a0003c0004t0001g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.280+27068A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71938435 | ||||||
| chrX:71938628
|
T | C | 2 | a0001c0001t0067g0148a0001c0003t0029g0149 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.280+27261T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71938628 | ||||||
| chrX:71938809
|
G | A | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+27442G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71938809 | ||||||
| chrX:71938894
|
A | G | 2 | a0003c0004t0063g0063a0004c0005t0082g0062 | 2 | NA18982.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.280+27527A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71938894 | ||||||
| chrX:71939140
|
T | A | 35 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(32): Show | 35 | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.280+27773T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71939140 | ||||||
| chrX:71939140
|
T | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.280+27773T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71939140 | ||||||
| chrX:71939180
|
G | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+27813G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71939180 | ||||||
| chrX:71940072
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.280+28705A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71940072 | ||||||
| chrX:71940142
|
G | A | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+28775G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71940142 | ||||||
| chrX:71940387
|
A | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+29020A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71940387 | ||||||
| chrX:71940456
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+29089G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71940456 | ||||||
| chrX:71940580
|
G | A | 2 | a0001c0001t0048g0168a0001c0012t0003g0169 | 2 | HG01515.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.280+29213G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71940580 | ||||||
| chrX:71940759
|
T | TG | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+29393dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71940759 | |||||
| chrX:71941006
|
G | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(25): Show | 28 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.280+29639G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71941006 | ||||||
| chrX:71941232
|
C | G | 92 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.280+29865C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71941232 | ||||||
| chrX:71941720
|
G | C | 1 | a0001c0001t0080g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.280+30353G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71941720 | ||||||
| chrX:71942025
|
G | C | 92 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.280+30658G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942025 | ||||||
| chrX:71942431
|
C | A | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+31064C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942431 | ||||||
| chrX:71942515
|
G | T | 94 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.280+31148G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942515 | ||||||
| chrX:71942836
|
A | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(25): Show | 28 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.280+31469A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942836 | ||||||
| chrX:71942849
|
A | G | 2 | a0001c0001t0010g0008a0001c0001t0064g0009 | 2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.280+31482A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942849 | ||||||
| chrX:71942925
|
A | G | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.280+31558A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942925 | ||||||
| chrX:71942934
|
C | T | 1 | a0002c0002t0002g0145 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.280+31567C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942934 | ||||||
| chrX:71942947
|
GCT | G | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280+31605_280+3160 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942947 | |||||
| chrX:71942964
|
C | G | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+31597C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942964 | ||||||
| chrX:71942966
|
C | A | 1 | a0002c0002t0076g0075 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.280+31599C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942966 | ||||||
| chrX:71942966
|
CTCTCTCT others(9): Show |
C | 6 | a0001c0001t0057g0103a0002c0002t0002g0086a0002c0002t0002g0101others(3): Show | 6 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+31601_280+3161 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942966 | |||||
| chrX:71942970
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+31604_280+3160 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942970 | |||||
| chrX:71942970
|
CTCTG | C | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+31605_280+3160 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942970 | |||||
| chrX:71942970
|
CTCTGTG | C | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+31605_280+3161 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942970 | |||||
| chrX:71942972
|
C | CTCTCTCT others(5): Show |
1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+31606_280+3160 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTCTCTG | 2 | a0001c0001t0001g0138a0001c0003t0029g0149 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.280+31606_280+3160 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTCTCTGT others(3): Show |
4 | a0001c0001t0001g0072a0001c0001t0001g0074a0003c0004t0008g0071others(1): Show | 4 | NA18971.hp1 NA18982.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+31606_280+3160 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTCTGTG | 2 | a0001c0001t0067g0148a0001c0003t0084g0150 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+31606_280+3160 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTCTGTGT others(3): Show |
19 | a0001c0001t0004g0066a0001c0001t0005g0146a0001c0001t0015g0135others(16): Show | 19 | HG01934.hp1 HG01943.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.280+31606_280+3160 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTCTGTGT others(5): Show |
1 | a0002c0002t0002g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280+31606_280+3160 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTCTGTGT others(9): Show |
1 | a0002c0002t0002g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.280+31606_280+3160 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTG | 1 | a0002c0002t0078g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.280+31639_280+3164 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTGTG | 6 | a0001c0001t0019g0160a0001c0001t0019g0161a0001c0001t0037g0154others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+31637_280+3164 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTGTGTGT others(1): Show |
1 | a0004c0005t0001g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.280+31633_280+3164 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.280+31631_280+3164 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTGTGTGT others(11): Show |
1 | a0002c0002t0002g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.280+31623_280+3164 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | CTGTGTGT others(13): Show |
1 | a0001c0019t0054g0070 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280+31621_280+3164 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0005g0096 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.280+31605C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942972 | ||||||
| chrX:71942972
|
CTG | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(39): Show | 42 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.280+31639_280+3164 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
CTGTG | C | 73 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(70): Show | 73 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.280+31637_280+3164 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
CTGTGTG | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+31635_280+3164 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
CTGTGTGT others(1): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.280+31633_280+3164 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942972
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0017g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.280+31631_280+3164 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71942972 | |||||
| chrX:71942974
|
G | C | 1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280+31607G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942974 | ||||||
| chrX:71942976
|
G | C | 17 | a0001c0001t0015g0049a0001c0001t0018g0132a0001c0001t0022g0052others(14): Show | 17 | HG02109.hp1 HG02698.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+31609G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942976 | ||||||
| chrX:71942978
|
G | C | 87 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(84): Show | 87 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.280+31611G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942978 | ||||||
| chrX:71942980
|
G | C | 87 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(84): Show | 87 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.280+31613G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942980 | ||||||
| chrX:71942982
|
G | C | 88 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(85): Show | 88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.280+31615G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942982 | ||||||
| chrX:71942984
|
G | C | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+31617G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71942984 | ||||||
| chrX:71943231
|
C | T | 1 | a0005c0006t0003g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.280+31864C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71943231 | ||||||
| chrX:71943237
|
C | A | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+31870C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71943237 | ||||||
| chrX:71943354
|
A | G | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.280+31987A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71943354 | ||||||
| chrX:71943619
|
G | A | 108 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.280+32252G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71943619 | ||||||
| chrX:71943871
|
G | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(28): Show | 31 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+32504G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71943871 | ||||||
| chrX:71943972
|
A | C | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.280+32605A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71943972 | ||||||
| chrX:71944079
|
T | C | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+32712T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944079 | ||||||
| chrX:71944152
|
C | T | 1 | a0004c0005t0082g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.280+32785C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944152 | ||||||
| chrX:71944158
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+32791A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944158 | ||||||
| chrX:71944291
|
G | C | 2 | a0001c0001t0009g0032a0001c0001t0020g0139 | 2 | NA18994.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.280+32924G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944291 | ||||||
| chrX:71944525
|
A | G | 16 | a0001c0001t0001g0053a0001c0001t0005g0091a0001c0001t0015g0049others(13): Show | 16 | HG01109.hp1 HG02109.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.280+33158A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944525 | ||||||
| chrX:71944537
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0065g0163 | 2 | HG02523.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.280+33170G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944537 | ||||||
| chrX:71944605
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+33238G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944605 | ||||||
| chrX:71944770
|
A | G | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0014t0040g0167others(3): Show | 6 | HG01169.hp2 HG01256.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+33403A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71944770 | ||||||
| chrX:71945124
|
T | TG | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+33764dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71945124 | |||||
| chrX:71945126
|
G | C | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+33759G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945126 | ||||||
| chrX:71945217
|
C | T | 3 | a0001c0001t0001g0138a0009c0010t0052g0185a0012c0018t0001g0147 | 3 | HG02257.hp2 HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+33850C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945217 | ||||||
| chrX:71945320
|
C | T | 1 | a0001c0001t0017g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.280+33953C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945320 | ||||||
| chrX:71945485
|
C | T | 1 | a0001c0001t0047g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.280+34118C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945485 | ||||||
| chrX:71945732
|
G | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.280+34365G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945732 | ||||||
| chrX:71945751
|
C | T | 1 | a0001c0013t0003g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.280+34384C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945751 | ||||||
| chrX:71945922
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.280+34555G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71945922 | ||||||
| chrX:71946042
|
A | G | 1 | a0001c0001t0014g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.280+34675A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71946042 | ||||||
| chrX:71946329
|
G | T | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+34962G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71946329 | ||||||
| chrX:71946691
|
C | T | 1 | a0001c0001t0016g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.280+35324C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71946691 | ||||||
| chrX:71946751
|
T | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+35384T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71946751 | ||||||
| chrX:71946966
|
G | C | 2 | a0001c0001t0022g0052a0001c0003t0036g0054 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.280+35599G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71946966 | ||||||
| chrX:71947166
|
G | A | 3 | a0001c0001t0037g0154a0001c0001t0051g0187a0002c0002t0002g0060 | 3 | HG03540.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+35799G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71947166 | ||||||
| chrX:71947319
|
TG | T | 1 | a0001c0001t0001g0033 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.280+35955delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71947319 | |||||
| chrX:71947516
|
A | C | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+36149A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71947516 | ||||||
| chrX:71947716
|
G | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(24): Show | 27 | HG00438.hp1 HG02015.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.280+36349G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71947716 | ||||||
| chrX:71947831
|
G | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+36464G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71947831 | ||||||
| chrX:71948097
|
A | G | 1 | a0001c0001t0041g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.280+36730A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71948097 | ||||||
| chrX:71948379
|
G | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+37012G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71948379 | ||||||
| chrX:71948395
|
A | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.280+37028A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71948395 | ||||||
| chrX:71948827
|
C | CA | 3 | a0001c0001t0019g0160a0001c0001t0019g0161a0001c0003t0070g0027 | 3 | HG01167.hp1 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280+37474dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948827 | |||||
| chrX:71948827
|
CA | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 39 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.280+37474delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948827 | |||||
| chrX:71948827
|
CAA | C | 84 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(81): Show | 84 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.280+37473_280+3747 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948827 | |||||
| chrX:71948846
|
G | GT | 2 | a0001c0001t0001g0115a0001c0001t0004g0116 | 2 | HG00621.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.280+37483dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948846 | |||||
| chrX:71948851
|
G | GT | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(126): Show | 129 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.280+37497dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948851 | |||||
| chrX:71948851
|
G | GTT | 3 | a0001c0001t0001g0098a0001c0001t0047g0117a0003c0004t0001g0043 | 3 | HG03834.hp1 NA19003.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.280+37496_280+3749 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948851 | |||||
| chrX:71948851
|
G | T | 2 | a0001c0001t0001g0115a0001c0001t0004g0116 | 2 | HG00621.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.280+37484G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71948851 | ||||||
| chrX:71948851
|
GT | G | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+37497delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948851 | |||||
| chrX:71948929
|
C | CT | 3 | a0001c0001t0037g0154a0001c0001t0051g0187a0002c0002t0002g0060 | 3 | HG03540.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+37571dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71948929 | |||||
| chrX:71948954
|
C | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(28): Show | 31 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+37587C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71948954 | ||||||
| chrX:71948995
|
T | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.280+37628T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71948995 | ||||||
| chrX:71949035
|
A | C | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+37668A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949035 | ||||||
| chrX:71949047
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+37680C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949047 | ||||||
| chrX:71949261
|
A | C | 31 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(28): Show | 31 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+37894A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949261 | ||||||
| chrX:71949383
|
A | G | 3 | a0001c0001t0060g0080a0005c0006t0016g0078a0005c0006t0058g0079 | 3 | HG01934.hp1 HG01943.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.280+38016A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949383 | ||||||
| chrX:71949526
|
C | T | 5 | a0001c0001t0057g0103a0002c0002t0002g0101a0002c0002t0002g0104others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+38159C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949526 | ||||||
| chrX:71949557
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+38190C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949557 | ||||||
| chrX:71949799
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0004g0116a0001c0001t0022g0127 | 3 | HG00621.hp1 HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.280+38432C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949799 | ||||||
| chrX:71949814
|
A | G | 22 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0015g0049others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.280+38447A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71949814 | ||||||
| chrX:71950254
|
C | A | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+38887C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71950254 | ||||||
| chrX:71950278
|
G | A | 1 | a0001c0001t0009g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.280+38911G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71950278 | ||||||
| chrX:71950346
|
G | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.280+38979G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71950346 | ||||||
| chrX:71950396
|
G | T | 1 | a0001c0012t0003g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.280+39029G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71950396 | ||||||
| chrX:71950668
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0009g0184others(3): Show | 6 | NA18965.hp1 NA18984.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+39301G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71950668 | ||||||
| chrX:71950991
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.280+39624C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71950991 | ||||||
| chrX:71951005
|
T | TAC | 41 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0098others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.280+39672_280+3967 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACAC | 28 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0114others(25): Show | 28 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.280+39670_280+3967 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACAC | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(23): Show | 26 | HG00738.hp1 HG02129.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.280+39668_280+3967 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(1): Show |
13 | a0001c0001t0001g0023a0001c0001t0003g0181a0001c0001t0017g0166others(10): Show | 13 | HG01069.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.280+39666_280+3967 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(3): Show |
11 | a0001c0001t0001g0053a0001c0001t0010g0002a0001c0001t0023g0055others(8): Show | 11 | HG01515.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+39664_280+3967 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0177a0001c0001t0022g0052a0001c0003t0011g0155others(5): Show | 8 | HG01169.hp2 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+39662_280+3967 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(7): Show |
4 | a0001c0001t0037g0154a0001c0015t0032g0031a0003c0004t0008g0003others(1): Show | 4 | HG02055.hp1 HG02615.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+39660_280+3967 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(9): Show |
11 | a0001c0001t0001g0034a0001c0001t0003g0050a0001c0001t0010g0008others(8): Show | 11 | HG01243.hp1 HG01952.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+39658_280+3967 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(11): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0033others(9): Show | 12 | HG00438.hp1 HG02015.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+39656_280+3967 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(13): Show |
12 | a0001c0001t0001g0041a0001c0001t0009g0040a0001c0001t0020g0042others(9): Show | 12 | HG02027.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.280+39654_280+3967 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951005
|
T | TACACACA others(15): Show |
2 | a0001c0001t0001g0010a0001c0001t0069g0048 | 2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.280+39652_280+3967 others(26): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951005 | |||||
| chrX:71951040
|
A | AC | 1 | a0001c0001t0003g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.280+39673_280+3967 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71951040 | ||||||
| chrX:71951040
|
A | ACACACAC | 2 | a0001c0001t0014g0173a0001c0001t0065g0163 | 2 | HG02738.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.280+39673_280+3967 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71951040 | ||||||
| chrX:71951040
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.280+39673_280+3967 others(17): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71951040 | ||||||
| chrX:71951040
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280+39673_280+3967 others(25): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71951040 | ||||||
| chrX:71951079
|
A | G | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+39712A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71951079 | ||||||
| chrX:71951430
|
A | G | 1 | a0001c0003t0012g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.280+40063A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71951430 | ||||||
| chrX:71951898
|
TTC | T | 1 | a0003c0004t0063g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.280+40535_280+4053 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71951898 | |||||
| chrX:71952016
|
C | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+40649C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71952016 | ||||||
| chrX:71952322
|
GC | G | 1 | a0001c0001t0001g0026 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.280+40959delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71952322 | |||||
| chrX:71952745
|
G | A | 6 | a0001c0001t0057g0103a0002c0002t0002g0086a0002c0002t0002g0101others(3): Show | 6 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+41378G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71952745 | ||||||
| chrX:71952760
|
C | T | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280+41393C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71952760 | ||||||
| chrX:71952804
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+41437T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71952804 | ||||||
| chrX:71952952
|
C | T | 4 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+41585C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71952952 | ||||||
| chrX:71953041
|
G | C | 22 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0015g0049others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.280+41674G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71953041 | ||||||
| chrX:71953200
|
A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(177): Show | 180 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.280+41833A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71953200 | ||||||
| chrX:71953282
|
G | A | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+41915G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71953282 | ||||||
| chrX:71953495
|
G | A | 22 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0015g0049others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.280+42128G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71953495 | ||||||
| chrX:71953692
|
G | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(28): Show | 31 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+42325G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71953692 | ||||||
| chrX:71953725
|
CT | C | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.280+42361delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71953725 | |||||
| chrX:71954151
|
G | GT | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+42787dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71954151 | |||||
| chrX:71954350
|
G | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0009g0184others(3): Show | 6 | NA18965.hp1 NA18984.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+42983G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71954350 | ||||||
| chrX:71954557
|
T | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.280+43190T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71954557 | ||||||
| chrX:71954825
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.280+43458G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71954825 | ||||||
| chrX:71955095
|
C | G | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+43728C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71955095 | ||||||
| chrX:71955225
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0021g0006a0001c0001t0021g0007 | 3 | NA18952.hp1 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.280+43858C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71955225 | ||||||
| chrX:71955286
|
T | G | 1 | a0005c0006t0016g0078 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.280+43919T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71955286 | ||||||
| chrX:71955699
|
AGCTGTGA others(13): Show |
A | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+44334_280+4435 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71955699 | |||||
| chrX:71955795
|
C | CT | 2 | a0001c0001t0048g0168a0001c0012t0003g0169 | 2 | HG01515.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.280+44442dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71955795 | |||||
| chrX:71955795
|
CT | C | 2 | a0001c0001t0001g0108a0001c0001t0004g0014 | 2 | NA19072.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.280+44442delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71955795 | |||||
| chrX:71955861
|
G | T | 113 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.280+44494G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71955861 | ||||||
| chrX:71956907
|
A | G | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(142): Show | 145 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.280+45540A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71956907 | ||||||
| chrX:71957129
|
G | A | 3 | a0001c0001t0037g0154a0001c0001t0051g0187a0002c0002t0002g0060 | 3 | HG03540.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+45762G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957129 | ||||||
| chrX:71957197
|
T | C | 3 | a0001c0001t0060g0080a0005c0006t0016g0078a0005c0006t0058g0079 | 3 | HG01934.hp1 HG01943.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.280+45830T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957197 | ||||||
| chrX:71957297
|
G | T | 12 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(9): Show | 12 | HG02109.hp1 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+45930G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957297 | ||||||
| chrX:71957307
|
G | A | 1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280+45940G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957307 | ||||||
| chrX:71957329
|
C | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+45962C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957329 | ||||||
| chrX:71957404
|
C | A | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+46037C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957404 | ||||||
| chrX:71957816
|
T | A | 103 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.280+46449T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957816 | ||||||
| chrX:71957905
|
G | A | 1 | a0003c0004t0008g0071 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.280+46538G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71957905 | ||||||
| chrX:71958034
|
C | T | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+46667C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958034 | ||||||
| chrX:71958110
|
C | T | 4 | a0001c0001t0023g0055a0001c0003t0012g0057a0001c0003t0012g0058others(1): Show | 4 | HG02809.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+46743C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958110 | ||||||
| chrX:71958114
|
C | G | 1 | a0001c0001t0001g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.280+46747C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958114 | ||||||
| chrX:71958171
|
C | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(69): Show | 72 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.280+46804C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958171 | ||||||
| chrX:71958535
|
G | A | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+47168G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958535 | ||||||
| chrX:71958878
|
G | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+47511G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958878 | ||||||
| chrX:71958997
|
G | A | 42 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0074others(39): Show | 42 | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.280+47630G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71958997 | ||||||
| chrX:71959071
|
C | A | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+47704C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959071 | ||||||
| chrX:71959134
|
T | C | 4 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+47767T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959134 | ||||||
| chrX:71959206
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 38 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.280+47839T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959206 | ||||||
| chrX:71959331
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 38 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.280+47964T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959331 | ||||||
| chrX:71959334
|
T | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+47967T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959334 | ||||||
| chrX:71959447
|
TA | T | 1 | a0001c0001t0001g0033 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.280+48086delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71959447 | |||||
| chrX:71959801
|
A | G | 4 | a0001c0019t0054g0070a0001c0020t0005g0012a0002c0002t0002g0067others(1): Show | 4 | HG00738.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+48434A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959801 | ||||||
| chrX:71959991
|
G | A | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.280+48624G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71959991 | ||||||
| chrX:71960380
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 38 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.280+49013T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71960380 | ||||||
| chrX:71960419
|
T | C | 1 | a0001c0015t0032g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.280+49052T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71960419 | ||||||
| chrX:71960578
|
A | G | 4 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+49211A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71960578 | ||||||
| chrX:71960732
|
G | T | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+49365G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71960732 | ||||||
| chrX:71961248
|
GAATTC | G | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+49883_280+4988 others(9): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71961248 | |||||
| chrX:71961310
|
T | C | 1 | a0001c0001t0069g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.280+49943T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71961310 | ||||||
| chrX:71961349
|
G | C | 1 | a0001c0003t0036g0054 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.280+49982G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71961349 | ||||||
| chrX:71961400
|
TCCTC | T | 1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280+50050_280+5005 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71961400 | |||||
| chrX:71961720
|
C | T | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+50353C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71961720 | ||||||
| chrX:71962089
|
C | A | 1 | a0005c0006t0058g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.280+50722C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71962089 | ||||||
| chrX:71962260
|
A | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(25): Show | 28 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.280+50893A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71962260 | ||||||
| chrX:71962627
|
CT | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(11): Show | 14 | HG02523.hp1 HG02647.hp1 HG06807.hp1 others(11): Show |
intron_variant | MODIFIER | c.280+51280delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71962627 | |||||
| chrX:71962627
|
CTT | C | 108 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.280+51279_280+5128 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71962627 | |||||
| chrX:71962627
|
CTTT | C | 5 | a0001c0001t0005g0091a0001c0001t0044g0164a0001c0003t0033g0093others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+51278_280+5128 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71962627 | |||||
| chrX:71962627
|
CTTTT | C | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+51277_280+5128 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71962627 | |||||
| chrX:71962838
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | NA18979.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.280+51471A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71962838 | ||||||
| chrX:71963071
|
T | C | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+51704T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963071 | ||||||
| chrX:71963298
|
AT | A | 1 | a0001c0003t0031g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280+51935delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963298 | |||||
| chrX:71963329
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.280+51962C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963329 | ||||||
| chrX:71963517
|
G | T | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.280+52150G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963517 | ||||||
| chrX:71963593
|
A | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(24): Show | 27 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.280+52226A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963593 | ||||||
| chrX:71963813
|
T | C | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+52446T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963813 | ||||||
| chrX:71963940
|
G | A | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+52573G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963940 | ||||||
| chrX:71963949
|
C | CTATATA | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+52587_280+5259 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963949 | |||||
| chrX:71963949
|
C | CTATATAT others(1): Show |
40 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(37): Show | 40 | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.280+52585_280+5259 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963949 | |||||
| chrX:71963958
|
T | TAC | 3 | a0001c0001t0001g0107a0001c0001t0038g0158a0001c0003t0028g0159 | 3 | HG00438.hp2 HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+52595_280+5259 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963958 | |||||
| chrX:71963960
|
C | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(27): Show | 30 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.280+52593C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963960 | ||||||
| chrX:71963962
|
C | CAT | 10 | a0001c0001t0001g0065a0001c0001t0005g0096a0001c0001t0039g0151others(7): Show | 10 | HG01928.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+52605_280+5260 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963962 | |||||
| chrX:71963962
|
C | CATAT | 6 | a0001c0001t0057g0103a0002c0002t0002g0101a0002c0002t0002g0104others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+52603_280+5260 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963962 | |||||
| chrX:71963962
|
C | CATATATA others(51): Show |
2 | a0001c0001t0003g0016a0001c0001t0065g0163 | 2 | NA19082.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.280+52606_280+5260 others(62): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963962 | |||||
| chrX:71963962
|
C | CATATATA others(51): Show |
1 | a0001c0001t0017g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.280+52606_280+5260 others(62): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963962 | |||||
| chrX:71963962
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+52595C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963962 | ||||||
| chrX:71963968
|
T | TATATATA others(1): Show |
7 | a0001c0001t0001g0099a0001c0001t0001g0115a0001c0001t0004g0116others(4): Show | 7 | HG00621.hp1 HG02055.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+52606_280+5260 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963968 | |||||
| chrX:71963970
|
T | TATATAC | 63 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0030others(60): Show | 63 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.280+52606_280+5260 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963970 | |||||
| chrX:71963970
|
T | TATATACA others(55): Show |
1 | a0001c0001t0004g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280+52606_280+5260 others(66): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963970 | |||||
| chrX:71963972
|
T | C | 2 | a0001c0001t0067g0148a0001c0003t0029g0149 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.280+52605T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963972 | ||||||
| chrX:71963972
|
T | TATAC | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(22): Show | 25 | HG00438.hp1 HG00673.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.280+52606_280+5260 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963972 | |||||
| chrX:71963972
|
T | TATACATA others(53): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(5): Show | 8 | HG02523.hp1 HG03490.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+52606_280+5260 others(64): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963972 | |||||
| chrX:71963973
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+52606A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963973 | ||||||
| chrX:71963974
|
C | CAT | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+52624_280+5262 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963974 | |||||
| chrX:71963974
|
C | CATAT | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.280+52622_280+5262 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963974 | |||||
| chrX:71963974
|
C | T | 138 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(135): Show | 138 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.280+52607C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963974 | ||||||
| chrX:71963975
|
A | G | 40 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(37): Show | 40 | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.280+52608A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963975 | ||||||
| chrX:71963976
|
T | C | 14 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0041others(11): Show | 14 | HG01243.hp1 HG02015.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.280+52609T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963976 | ||||||
| chrX:71963976
|
T | TAC | 1 | a0001c0001t0051g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280+52610_280+5261 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963976 | |||||
| chrX:71963976
|
T | TATATATA others(45): Show |
1 | a0003c0004t0061g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.280+52625_280+5262 others(56): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963976 | |||||
| chrX:71963976
|
T | TATATATA others(51): Show |
1 | a0001c0001t0046g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.280+52625_280+5262 others(62): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963976 | |||||
| chrX:71963978
|
T | TACATATA others(55): Show |
1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+52612_280+5261 others(66): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963978 | |||||
| chrX:71963978
|
T | TATATATA others(49): Show |
1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.280+52625_280+5262 others(60): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963978 | |||||
| chrX:71963979
|
A | ATATATAT others(5): Show |
1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+52621_280+5262 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963979 | |||||
| chrX:71963980
|
T | C | 2 | a0001c0001t0066g0046a0001c0001t0072g0038 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.280+52613T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963980 | ||||||
| chrX:71963982
|
T | C | 2 | a0001c0001t0066g0046a0001c0001t0072g0038 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.280+52615T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963982 | ||||||
| chrX:71963983
|
A | ATATATGT others(1): Show |
1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+52621_280+5262 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963983 | |||||
| chrX:71963983
|
A | ATATGTAT others(15): Show |
2 | a0001c0001t0001g0051a0001c0001t0003g0050 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.280+52619_280+5262 others(26): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963983 | |||||
| chrX:71963983
|
A | ATATGTGT others(1): Show |
1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+52619_280+5262 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963983 | |||||
| chrX:71963983
|
A | ATGTATAT others(13): Show |
2 | a0001c0001t0067g0148a0001c0003t0029g0149 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.280+52617_280+5261 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963983 | |||||
| chrX:71963985
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(9): Show | 12 | HG00438.hp1 HG02027.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+52618A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963985 | ||||||
| chrX:71963987
|
A | ATGTGTAT others(23): Show |
2 | a0001c0001t0056g0092a0001c0003t0033g0093 | 2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+52621_280+5262 others(34): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963987 | |||||
| chrX:71963987
|
A | ATGTGTAT others(49): Show |
1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280+52621_280+5262 others(60): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963987 | |||||
| chrX:71963987
|
A | G | 11 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0041others(8): Show | 11 | HG02015.hp1 HG02040.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+52620A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963987 | ||||||
| chrX:71963989
|
A | G | 2 | a0001c0001t0074g0142a0009c0010t0052g0185 | 2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.280+52622A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963989 | ||||||
| chrX:71963991
|
A | ATATATAT others(3): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(5): Show | 8 | HG00438.hp1 NA18952.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+52625_280+5262 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963991 | |||||
| chrX:71963991
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0041 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.280+52625_280+5262 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963991 | |||||
| chrX:71963991
|
A | ATATATGT others(3): Show |
4 | a0001c0001t0001g0033a0001c0001t0009g0032a0001c0001t0020g0042others(1): Show | 4 | HG02027.hp1 NA18948.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+52625_280+5262 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963991 | |||||
| chrX:71963991
|
A | G | 35 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(32): Show | 35 | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.280+52624A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963991 | ||||||
| chrX:71963993
|
G | A | 13 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0045others(10): Show | 13 | HG02015.hp1 HG02074.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.280+52626G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963993 | ||||||
| chrX:71963995
|
A | ATG | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+52629_280+5263 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71963995 | |||||
| chrX:71963997
|
A | G | 5 | a0001c0001t0001g0051a0001c0001t0001g0138a0001c0001t0003g0050others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+52630A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963997 | ||||||
| chrX:71963999
|
A | ATATGTAT others(1): Show |
47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(44): Show | 47 | HG00438.hp1 HG00738.hp1 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+52632_280+5263 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963999 | ||||||
| chrX:71963999
|
A | ATATGTAT others(25): Show |
1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+52632_280+5263 others(36): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963999 | ||||||
| chrX:71963999
|
A | ATGTGTGT others(13): Show |
10 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0045others(7): Show | 10 | HG02015.hp1 HG02074.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+52632_280+5263 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963999 | ||||||
| chrX:71963999
|
A | G | 3 | a0001c0001t0056g0092a0001c0003t0033g0093a0001c0003t0035g0133 | 3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.280+52632A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71963999 | ||||||
| chrX:71964000
|
C | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 70 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.280+52633C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964000 | ||||||
| chrX:71964005
|
A | G | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+52638A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964005 | ||||||
| chrX:71964007
|
A | G | 3 | a0001c0001t0066g0046a0001c0001t0072g0038a0001c0003t0084g0150 | 3 | HG02523.hp2 HG02965.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.280+52640A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964007 | ||||||
| chrX:71964009
|
A | ATG | 3 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031 | 3 | HG02615.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.280+52644_280+5264 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964009 | |||||
| chrX:71964009
|
A | G | 4 | a0001c0001t0066g0046a0001c0001t0067g0148a0001c0001t0072g0038others(1): Show | 4 | HG02109.hp2 HG02523.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+52642A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964009 | ||||||
| chrX:71964011
|
G | A | 2 | a0001c0003t0084g0150a0009c0010t0052g0185 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.280+52644G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964011 | ||||||
| chrX:71964011
|
G | GTGTA | 13 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.280+52645_280+5264 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964011 | |||||
| chrX:71964011
|
GTA | G | 8 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(5): Show | 8 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+52656_280+5265 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964011 | |||||
| chrX:71964011
|
GTATATAT others(27): Show |
G | 1 | a0002c0002t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.280+52656_280+5268 others(38): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964011 | |||||
| chrX:71964013
|
A | G | 86 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.280+52646A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964013 | ||||||
| chrX:71964017
|
A | ATATATG | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+52655_280+5265 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964017 | |||||
| chrX:71964017
|
A | G | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+52650A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964017 | ||||||
| chrX:71964019
|
A | ATATG | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(21): Show | 24 | HG00438.hp1 HG01243.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.280+52655_280+5265 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964019 | |||||
| chrX:71964019
|
A | ATG | 2 | a0001c0001t0067g0148a0001c0003t0029g0149 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.280+52653_280+5265 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964019 | |||||
| chrX:71964019
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+52652A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964019 | ||||||
| chrX:71964021
|
A | ATG | 35 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0037others(32): Show | 35 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.280+52655_280+5265 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964021 | |||||
| chrX:71964021
|
A | G | 2 | a0001c0001t0066g0046a0001c0001t0072g0038 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.280+52654A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964021 | ||||||
| chrX:71964023
|
A | ATACATAT others(73): Show |
1 | a0001c0001t0042g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.280+52657_280+5265 others(84): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964023 | |||||
| chrX:71964023
|
A | ATACATAT others(49): Show |
56 | a0001c0001t0001g0023a0001c0001t0001g0089a0001c0001t0001g0094others(53): Show | 56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.280+52657_280+5265 others(60): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964023 | |||||
| chrX:71964023
|
A | ATACATAT others(47): Show |
1 | a0002c0002t0007g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.280+52657_280+5265 others(58): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964023 | |||||
| chrX:71964023
|
A | ATACATAT others(47): Show |
8 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0003g0181others(5): Show | 8 | HG00621.hp1 HG00642.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+52657_280+5265 others(58): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964023 | |||||
| chrX:71964023
|
A | ATACATAT others(45): Show |
1 | a0001c0001t0001g0100 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.280+52657_280+5265 others(56): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964023 | |||||
| chrX:71964023
|
A | ATGTGTG | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(13): Show | 16 | HG00280.hp1 HG01928.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.280+52661_280+5266 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964023 | |||||
| chrX:71964023
|
A | G | 16 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(13): Show | 16 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.280+52656A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964023 | ||||||
| chrX:71964025
|
G | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(61): Show | 64 | HG00438.hp1 HG00738.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.280+52658G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964025 | ||||||
| chrX:71964027
|
G | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 70 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.280+52660G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964027 | ||||||
| chrX:71964027
|
G | GTA | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+52674_280+5267 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964027 | |||||
| chrX:71964027
|
G | GTGTA | 3 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031 | 3 | HG02615.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.280+52661_280+5266 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964027 | |||||
| chrX:71964027
|
G | GTGTGTGT others(1): Show |
2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+52661_280+5266 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964027 | |||||
| chrX:71964029
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0066g0046a0001c0001t0072g0038 | 2 | HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.280+52669_280+5267 others(34): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964029 | |||||
| chrX:71964029
|
A | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00438.hp1 HG01243.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+52662A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964029 | ||||||
| chrX:71964031
|
A | ATATATAT others(1): Show |
4 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+52671_280+5267 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964031 | |||||
| chrX:71964031
|
A | G | 35 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0037others(32): Show | 35 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.280+52664A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964031 | ||||||
| chrX:71964041
|
A | ATG | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+52676_280+5267 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964041 | |||||
| chrX:71964041
|
A | G | 44 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0089others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.280+52674A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964041 | ||||||
| chrX:71964043
|
G | A | 80 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0035others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.280+52676G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964043 | ||||||
| chrX:71964043
|
G | GTA | 56 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(53): Show | 56 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.280+52688_280+5268 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964043 | |||||
| chrX:71964043
|
G | GTATA | 1 | a0001c0001t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+52686_280+5268 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964043 | |||||
| chrX:71964043
|
GTA | G | 6 | a0001c0001t0057g0103a0002c0002t0002g0086a0002c0002t0002g0101others(3): Show | 6 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+52688_280+5268 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71964043 | |||||
| chrX:71964045
|
A | G | 36 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(33): Show | 36 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.280+52678A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964045 | ||||||
| chrX:71964211
|
C | T | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+52844C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964211 | ||||||
| chrX:71964230
|
C | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+52863C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964230 | ||||||
| chrX:71964301
|
G | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 70 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.280+52934G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964301 | ||||||
| chrX:71964636
|
A | T | 1 | a0001c0013t0003g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.280+53269A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964636 | ||||||
| chrX:71964650
|
C | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 70 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.280+53283C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71964650 | ||||||
| chrX:71965215
|
G | A | 2 | a0004c0005t0001g0087a0004c0005t0001g0088 | 2 | NA18955.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.280+53848G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71965215 | ||||||
| chrX:71965304
|
A | G | 4 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+53937A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71965304 | ||||||
| chrX:71965551
|
TC | T | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+54185delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71965551 | ||||||
| chrX:71965580
|
C | T | 3 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031 | 3 | HG02615.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.280+54213C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71965580 | ||||||
| chrX:71965581
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+54214G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71965581 | ||||||
| chrX:71965746
|
A | G | 4 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+54379A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71965746 | ||||||
| chrX:71966379
|
TG | T | 1 | a0001c0001t0009g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280+55015delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71966379 | |||||
| chrX:71966627
|
GC | G | 34 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(31): Show | 34 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(31): Show |
intron_variant | MODIFIER | c.280+55262delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71966627 | |||||
| chrX:71966838
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+55471A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71966838 | ||||||
| chrX:71967279
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+55912T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967279 | ||||||
| chrX:71967281
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.280+55914G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967281 | ||||||
| chrX:71967420
|
G | C | 42 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0089others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.280+56053G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967420 | ||||||
| chrX:71967663
|
A | C | 81 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.280+56296A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967663 | ||||||
| chrX:71967664
|
T | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(71): Show | 74 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(71): Show |
intron_variant | MODIFIER | c.280+56297T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967664 | ||||||
| chrX:71967840
|
C | T | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+56473C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967840 | ||||||
| chrX:71967888
|
T | C | 47 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(44): Show | 47 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.280+56521T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71967888 | ||||||
| chrX:71967996
|
C | CT | 1 | a0001c0001t0026g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.280+56644dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71967996 | |||||
| chrX:71967996
|
CT | C | 5 | a0001c0001t0019g0160a0001c0001t0025g0015a0003c0004t0006g0082others(2): Show | 5 | HG01169.hp1 HG02257.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+56644delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71967996 | |||||
| chrX:71968417
|
C | T | 1 | a0005c0006t0003g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.280+57050C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71968417 | ||||||
| chrX:71968557
|
A | T | 1 | a0006c0007t0013g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280+57190A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71968557 | ||||||
| chrX:71968725
|
C | G | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+57358C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71968725 | ||||||
| chrX:71969014
|
T | C | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+57647T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71969014 | ||||||
| chrX:71969168
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+57801T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71969168 | ||||||
| chrX:71969298
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+57952_280+5796 others(17): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71969298 | |||||
| chrX:71969298
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0003t0029g0149others(4): Show | 7 | HG01169.hp2 HG01256.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+57952_280+5796 others(17): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71969298 | |||||
| chrX:71969306
|
C | CT | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(8): Show | 11 | HG02523.hp1 NA18944.hp1 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+57951dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71969306 | |||||
| chrX:71969306
|
CT | C | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+57951delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71969306 | |||||
| chrX:71969319
|
C | CT | 52 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0035others(49): Show | 52 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.280+57965dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71969319 | |||||
| chrX:71969373
|
C | T | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+58006C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71969373 | ||||||
| chrX:71969501
|
C | T | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+58134C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71969501 | ||||||
| chrX:71970099
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+58732G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71970099 | ||||||
| chrX:71970462
|
C | T | 2 | a0001c0001t0037g0154a0001c0001t0051g0187 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+59095C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71970462 | ||||||
| chrX:71970596
|
T | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+59229T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71970596 | ||||||
| chrX:71970629
|
C | CT | 82 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.280+59274dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71970629 | |||||
| chrX:71970629
|
C | CTT | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+59273_280+5927 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71970629 | |||||
| chrX:71970629
|
CT | C | 2 | a0001c0001t0001g0010a0001c0001t0009g0032 | 2 | NA19056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.280+59274delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71970629 | |||||
| chrX:71970718
|
T | G | 2 | a0001c0001t0001g0094a0002c0002t0002g0095 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.280+59351T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71970718 | ||||||
| chrX:71970931
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+59564C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71970931 | ||||||
| chrX:71970933
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0009g0184others(3): Show | 6 | NA18965.hp1 NA18984.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+59566C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71970933 | ||||||
| chrX:71971172
|
TA | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+59811delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71971172 | |||||
| chrX:71971295
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+59928G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71971295 | ||||||
| chrX:71971313
|
G | A | 1 | a0001c0001t0005g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280+59946G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71971313 | ||||||
| chrX:71971617
|
G | A | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+60250G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71971617 | ||||||
| chrX:71971630
|
A | AT | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+60267dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71971630 | |||||
| chrX:71971645
|
T | G | 33 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(30): Show | 33 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.280+60278T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71971645 | ||||||
| chrX:71971839
|
T | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+60472T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71971839 | ||||||
| chrX:71972012
|
G | A | 2 | a0001c0001t0001g0094a0002c0002t0002g0095 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.280+60645G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972012 | ||||||
| chrX:71972038
|
CT | C | 1 | a0001c0001t0023g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.280+60683delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972038 | |||||
| chrX:71972317
|
G | A | 3 | a0001c0001t0023g0055a0001c0003t0035g0133a0002c0002t0002g0056 | 3 | HG02895.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.280+60950G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972317 | ||||||
| chrX:71972327
|
G | A | 2 | a0001c0001t0004g0066a0002c0002t0076g0075 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.280+60960G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972327 | ||||||
| chrX:71972331
|
G | A | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+60964G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972331 | ||||||
| chrX:71972594
|
C | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(170): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.280+61227C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972594 | ||||||
| chrX:71972853
|
C | A | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+61486C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972853 | ||||||
| chrX:71972866
|
T | TTG | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.280+61533_280+6153 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972866 | |||||
| chrX:71972866
|
T | TTGTG | 11 | a0001c0001t0001g0017a0001c0001t0001g0047a0001c0001t0037g0154others(8): Show | 11 | HG02083.hp1 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+61531_280+6153 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972866 | |||||
| chrX:71972866
|
T | TTGTGTG | 25 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0015g0049others(22): Show | 25 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.280+61529_280+6153 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972866 | |||||
| chrX:71972866
|
T | TTGTGTGT others(1): Show |
21 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0001g0074others(18): Show | 21 | HG00738.hp1 HG01943.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.280+61527_280+6153 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972866 | |||||
| chrX:71972866
|
T | TTGTGTGT others(3): Show |
8 | a0001c0001t0003g0144a0001c0001t0005g0146a0001c0001t0074g0142others(5): Show | 8 | HG02258.hp1 HG02970.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+61525_280+6153 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972866 | |||||
| chrX:71972866
|
TTGTGTG | T | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+61529_280+6153 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972866 | |||||
| chrX:71972901
|
T | TGTGTGTG others(4): Show |
1 | a0002c0002t0002g0145 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.280+61534_280+6153 others(15): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972901 | ||||||
| chrX:71972965
|
C | CTAT | 1 | a0001c0001t0016g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.280+61601_280+6160 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71972965 | |||||
| chrX:71972970
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+61603A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71972970 | ||||||
| chrX:71973508
|
C | T | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+62141C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71973508 | ||||||
| chrX:71973950
|
C | T | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+62583C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71973950 | ||||||
| chrX:71973962
|
A | G | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+62595A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71973962 | ||||||
| chrX:71973985
|
T | C | 1 | a0002c0002t0059g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.280+62618T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71973985 | ||||||
| chrX:71974035
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+62668A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71974035 | ||||||
| chrX:71974079
|
G | A | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+62712G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71974079 | ||||||
| chrX:71974200
|
C | T | 1 | a0002c0002t0002g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.280+62833C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71974200 | ||||||
| chrX:71974417
|
A | G | 1 | a0005c0006t0003g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.280+63050A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71974417 | ||||||
| chrX:71975011
|
TC | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+63649delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71975011 | |||||
| chrX:71975145
|
C | T | 1 | a0001c0001t0045g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.280+63778C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71975145 | ||||||
| chrX:71975235
|
C | T | 1 | a0003c0004t0001g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.280+63868C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71975235 | ||||||
| chrX:71975360
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | NA18970.hp1 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.280+63993C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71975360 | ||||||
| chrX:71975782
|
G | C | 1 | a0001c0001t0022g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.280+64415G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71975782 | ||||||
| chrX:71975921
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+64554A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71975921 | ||||||
| chrX:71976018
|
C | G | 4 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+64651C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976018 | ||||||
| chrX:71976208
|
G | A | 1 | a0001c0003t0029g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.280+64841G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976208 | ||||||
| chrX:71976322
|
A | C | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+64955A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976322 | ||||||
| chrX:71976418
|
A | C | 1 | a0001c0001t0026g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.280+65051A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976418 | ||||||
| chrX:71976569
|
TA | T | 1 | a0001c0001t0072g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.280+65204delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71976569 | |||||
| chrX:71976571
|
A | T | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.280+65204A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976571 | ||||||
| chrX:71976643
|
G | A | 2 | a0001c0001t0010g0002a0001c0001t0081g0081 | 2 | HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.280+65276G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976643 | ||||||
| chrX:71976761
|
A | G | 3 | a0001c0001t0001g0138a0009c0010t0052g0185a0012c0018t0001g0147 | 3 | HG02257.hp2 HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+65394A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976761 | ||||||
| chrX:71976773
|
T | C | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+65406T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71976773 | ||||||
| chrX:71976821
|
TGA | T | 2 | a0001c0001t0048g0168a0001c0012t0003g0169 | 2 | HG01515.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.280+65461_280+6546 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71976821 | |||||
| chrX:71977070
|
T | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+65703T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977070 | ||||||
| chrX:71977071
|
T | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+65704T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977071 | ||||||
| chrX:71977194
|
T | G | 4 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+65827T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977194 | ||||||
| chrX:71977205
|
A | G | 48 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(45): Show | 48 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.280+65838A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977205 | ||||||
| chrX:71977215
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+65848C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977215 | ||||||
| chrX:71977240
|
C | T | 4 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+65873C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977240 | ||||||
| chrX:71977425
|
C | CT | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.280+66074dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71977425 | |||||
| chrX:71977425
|
C | CTT | 14 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0041others(11): Show | 14 | HG02027.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+66073_280+6607 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71977425 | |||||
| chrX:71977425
|
C | CTTT | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+66072_280+6607 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71977425 | |||||
| chrX:71977425
|
CT | C | 2 | a0002c0002t0002g0060a0002c0002t0002g0086 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.280+66074delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71977425 | |||||
| chrX:71977427
|
T | C | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+66060T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977427 | ||||||
| chrX:71977502
|
G | A | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+66135G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977502 | ||||||
| chrX:71977694
|
T | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.280+66327T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71977694 | ||||||
| chrX:71978072
|
C | T | 48 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(45): Show | 48 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.280+66705C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978072 | ||||||
| chrX:71978084
|
G | A | 4 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+66717G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978084 | ||||||
| chrX:71978261
|
A | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.280+66894A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978261 | ||||||
| chrX:71978266
|
A | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.280+66899A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978266 | ||||||
| chrX:71978532
|
C | T | 1 | a0002c0002t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.280+67165C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978532 | ||||||
| chrX:71978684
|
C | CT | 1 | a0001c0001t0001g0074 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.280+67333dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71978684 | |||||
| chrX:71978684
|
CT | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0170others(4): Show | 7 | HG01433.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+67333delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71978684 | |||||
| chrX:71978756
|
G | GT | 4 | a0001c0001t0001g0037a0001c0001t0005g0096a0002c0002t0002g0141others(1): Show | 4 | HG02015.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+67406dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71978756 | |||||
| chrX:71978756
|
GT | G | 89 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.280+67406delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71978756 | |||||
| chrX:71978756
|
GTT | G | 1 | a0002c0002t0059g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.280+67405_280+6740 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71978756 | |||||
| chrX:71978762
|
T | G | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+67395T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978762 | ||||||
| chrX:71978985
|
C | G | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280+67618C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71978985 | ||||||
| chrX:71979128
|
T | C | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+67761T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979128 | ||||||
| chrX:71979174
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+67807A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979174 | ||||||
| chrX:71979210
|
A | G | 1 | a0001c0001t0009g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280+67843A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979210 | ||||||
| chrX:71979213
|
G | A | 1 | a0001c0001t0009g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280+67846G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979213 | ||||||
| chrX:71979235
|
G | C | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+67868G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979235 | ||||||
| chrX:71979294
|
T | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.280+67927T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979294 | ||||||
| chrX:71979406
|
G | A | 50 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(47): Show | 50 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.280+68039G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979406 | ||||||
| chrX:71979446
|
C | T | 1 | a0001c0003t0034g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.280+68079C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979446 | ||||||
| chrX:71979731
|
A | G | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+68364A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979731 | ||||||
| chrX:71979783
|
A | G | 1 | a0001c0001t0003g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.280+68416A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71979783 | ||||||
| chrX:71980019
|
A | C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(184): Show | 187 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.280+68652A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980019 | ||||||
| chrX:71980048
|
G | A | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+68681G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980048 | ||||||
| chrX:71980097
|
C | T | 2 | a0003c0004t0063g0063a0004c0005t0082g0062 | 2 | NA18982.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.280+68730C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980097 | ||||||
| chrX:71980243
|
A | G | 3 | a0001c0001t0001g0094a0002c0002t0002g0095a0006c0007t0013g0090 | 3 | HG02055.hp1 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.280+68876A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980243 | ||||||
| chrX:71980370
|
G | C | 4 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+69003G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980370 | ||||||
| chrX:71980551
|
TGTGTGTG others(2): Show |
T | 5 | a0001c0001t0001g0030a0001c0003t0030g0152a0001c0003t0034g0153others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+69201_280+6920 others(13): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980551 | |||||
| chrX:71980554
|
GTGTGGGG others(16): Show |
G | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+69188_280+6921 others(27): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980554 | ||||||
| chrX:71980557
|
T | G | 1 | a0001c0001t0022g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280+69190T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980557 | ||||||
| chrX:71980559
|
GGGTGTGT others(7): Show |
G | 1 | a0001c0001t0023g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.280+69194_280+6920 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980559 | |||||
| chrX:71980560
|
GGTGTGTG others(4): Show |
G | 4 | a0001c0001t0038g0158a0001c0003t0028g0159a0001c0003t0070g0027others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+69201_280+6921 others(15): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980560 | |||||
| chrX:71980560
|
GGTGTGTG others(6): Show |
G | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+69201_280+6921 others(17): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980560 | |||||
| chrX:71980560
|
GGTGTGTG others(8): Show |
G | 18 | a0001c0001t0001g0053a0001c0001t0005g0096a0001c0001t0015g0049others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+69201_280+6921 others(19): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980560 | |||||
| chrX:71980560
|
GGTGTGTG others(10): Show |
G | 31 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(28): Show | 31 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+69201_280+6921 others(21): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980560 | |||||
| chrX:71980560
|
GGTGTGTG others(12): Show |
G | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.280+69201_280+6921 others(23): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980560 | |||||
| chrX:71980560
|
GGTGTGTG others(14): Show |
G | 87 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(84): Show | 87 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.280+69201_280+6922 others(25): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71980560 | |||||
| chrX:71980577
|
T | G | 4 | a0001c0001t0022g0052a0001c0003t0011g0155a0001c0003t0011g0156others(1): Show | 4 | HG02976.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+69210T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980577 | ||||||
| chrX:71980579
|
T | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+69212T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980579 | ||||||
| chrX:71980593
|
T | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+69226T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980593 | ||||||
| chrX:71980655
|
C | T | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+69288C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980655 | ||||||
| chrX:71980680
|
G | A | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+69313G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980680 | ||||||
| chrX:71980823
|
C | T | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.280+69456C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71980823 | ||||||
| chrX:71981343
|
C | T | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+69976C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981343 | ||||||
| chrX:71981344
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+69977A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981344 | ||||||
| chrX:71981392
|
G | A | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+70025G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981392 | ||||||
| chrX:71981474
|
T | C | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+70107T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981474 | ||||||
| chrX:71981492
|
G | A | 1 | a0001c0011t0003g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280+70125G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981492 | ||||||
| chrX:71981536
|
C | CA | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.280+70187dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71981536 | |||||
| chrX:71981536
|
C | CAA | 65 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0035others(62): Show | 65 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(62): Show |
intron_variant | MODIFIER | c.280+70186_280+7018 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71981536 | |||||
| chrX:71981536
|
C | CAAA | 4 | a0001c0001t0037g0154a0001c0001t0038g0158a0001c0003t0028g0159others(1): Show | 4 | HG02451.hp1 HG03225.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+70185_280+7018 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71981536 | |||||
| chrX:71981899
|
A | G | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+70532A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981899 | ||||||
| chrX:71981994
|
A | G | 3 | a0001c0001t0004g0066a0002c0002t0002g0118a0002c0002t0076g0075 | 3 | HG02735.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.280+70627A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71981994 | ||||||
| chrX:71982049
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+70682A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71982049 | ||||||
| chrX:71982569
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0004g0116a0001c0001t0022g0127 | 3 | HG00621.hp1 HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.280+71202C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71982569 | ||||||
| chrX:71982762
|
C | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.280+71395C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71982762 | ||||||
| chrX:71982973
|
C | T | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+71606C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71982973 | ||||||
| chrX:71982979
|
C | G | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+71612C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71982979 | ||||||
| chrX:71983091
|
G | A | 48 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(45): Show | 48 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.280+71724G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983091 | ||||||
| chrX:71983195
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0004g0116a0001c0001t0022g0127 | 3 | HG00621.hp1 HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.280+71828C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983195 | ||||||
| chrX:71983334
|
A | G | 1 | a0001c0001t0017g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.280+71967A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983334 | ||||||
| chrX:71983441
|
C | CA | 1 | a0005c0006t0058g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.280+72088dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71983441 | |||||
| chrX:71983441
|
CA | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.280+72088delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71983441 | |||||
| chrX:71983677
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+72310A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983677 | ||||||
| chrX:71983887
|
T | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+72520T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983887 | ||||||
| chrX:71983967
|
G | A | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+72600G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983967 | ||||||
| chrX:71983988
|
C | G | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+72621C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71983988 | ||||||
| chrX:71984226
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.280+72859A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71984226 | ||||||
| chrX:71984236
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(25): Show | 28 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.280+72869C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71984236 | ||||||
| chrX:71984826
|
C | CT | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(139): Show | 142 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.280+73474dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71984826 | |||||
| chrX:71984826
|
C | CTT | 4 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+73473_280+7347 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71984826 | |||||
| chrX:71984861
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.280+73494T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71984861 | ||||||
| chrX:71984887
|
G | A | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+73520G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71984887 | ||||||
| chrX:71985065
|
C | T | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+73698C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71985065 | ||||||
| chrX:71985168
|
C | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.280+73801C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71985168 | ||||||
| chrX:71985449
|
T | G | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+74082T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71985449 | ||||||
| chrX:71985499
|
T | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.280+74132T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71985499 | ||||||
| chrX:71985688
|
T | G | 57 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(54): Show | 57 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.280+74321T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71985688 | ||||||
| chrX:71986001
|
A | C | 1 | a0001c0001t0001g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.280+74634A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71986001 | ||||||
| chrX:71986382
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+75015C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71986382 | ||||||
| chrX:71986516
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(25): Show | 28 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.280+75149G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71986516 | ||||||
| chrX:71986556
|
C | A | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.280+75189C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71986556 | ||||||
| chrX:71986802
|
T | C | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+75435T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71986802 | ||||||
| chrX:71986968
|
G | GA | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.280+75610dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71986968 | |||||
| chrX:71987210
|
C | CA | 11 | a0001c0001t0019g0160a0001c0001t0019g0161a0001c0001t0037g0154others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+75853dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71987210 | |||||
| chrX:71987394
|
C | T | 1 | a0001c0001t0022g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280+76027C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71987394 | ||||||
| chrX:71987534
|
C | G | 2 | a0001c0001t0001g0094a0002c0002t0002g0095 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.280+76167C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71987534 | ||||||
| chrX:71988446
|
A | G | 5 | a0001c0001t0001g0030a0001c0003t0070g0027a0001c0015t0032g0031others(2): Show | 5 | HG02257.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+77079A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988446 | ||||||
| chrX:71988512
|
G | A | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.280+77145G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988512 | ||||||
| chrX:71988524
|
G | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+77157G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988524 | ||||||
| chrX:71988546
|
G | T | 1 | a0002c0002t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280+77179G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988546 | ||||||
| chrX:71988585
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+77218C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988585 | ||||||
| chrX:71988616
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+77249T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988616 | ||||||
| chrX:71988875
|
G | A | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+77508G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71988875 | ||||||
| chrX:71989125
|
CT | C | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+77760delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989125 | |||||
| chrX:71989219
|
C | T | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+77852C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989219 | ||||||
| chrX:71989221
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.280+77854C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989221 | ||||||
| chrX:71989231
|
G | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+77864G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989231 | ||||||
| chrX:71989241
|
CG | C | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+77877delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989241 | |||||
| chrX:71989264
|
G | GC | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+77898dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989264 | |||||
| chrX:71989285
|
C | T | 3 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG01109.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.280+77918C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989285 | ||||||
| chrX:71989322
|
C | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | NA18970.hp1 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.280+77955C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989322 | ||||||
| chrX:71989348
|
C | CA | 14 | a0001c0001t0001g0010a0001c0001t0010g0084a0001c0001t0037g0154others(11): Show | 14 | HG02451.hp1 HG02572.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+78001dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989348 | |||||
| chrX:71989348
|
C | CAA | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.280+78000_280+7800 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989348 | |||||
| chrX:71989348
|
C | CAAA | 52 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0028others(49): Show | 52 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.280+77999_280+7800 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989348 | |||||
| chrX:71989348
|
C | CAAAA | 4 | a0001c0001t0015g0049a0001c0003t0012g0057a0002c0002t0002g0141others(1): Show | 4 | HG01934.hp1 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+77998_280+7800 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989348 | |||||
| chrX:71989433
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+78066A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989433 | ||||||
| chrX:71989437
|
A | G | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.280+78070A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989437 | ||||||
| chrX:71989653
|
G | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.280+78286G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989653 | ||||||
| chrX:71989680
|
AT | A | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+78318delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989680 | |||||
| chrX:71989790
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.280+78423C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989790 | ||||||
| chrX:71989852
|
A | AG | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+78487dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71989852 | |||||
| chrX:71989927
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(28): Show | 31 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.280+78560G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989927 | ||||||
| chrX:71989947
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+78580G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71989947 | ||||||
| chrX:71990040
|
T | TG | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+78675dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71990040 | |||||
| chrX:71990049
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.280+78682G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71990049 | ||||||
| chrX:71990342
|
C | CA | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+78976dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71990342 | |||||
| chrX:71990496
|
C | CT | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+79131dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71990496 | |||||
| chrX:71990554
|
A | AC | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+79191dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71990554 | |||||
| chrX:71990632
|
C | T | 48 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0053others(45): Show | 48 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.280+79265C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71990632 | ||||||
| chrX:71991102
|
T | TC | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+79737dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991102 | |||||
| chrX:71991392
|
C | G | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+80025C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71991392 | ||||||
| chrX:71991448
|
A | AT | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+80082dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991448 | |||||
| chrX:71991812
|
TTCTCTTT others(1): Show |
T | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+80451_280+8045 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991812 | |||||
| chrX:71991818
|
T | TTC | 30 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0037others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.280+80483_280+8048 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTC | 10 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0004g0066others(7): Show | 10 | HG02630.hp2 HG02735.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+80481_280+8048 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTCTC | 1 | a0002c0002t0002g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.280+80479_280+8048 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTCTCT others(1): Show |
22 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0001g0074others(19): Show | 22 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.280+80477_280+8048 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTCTCT others(3): Show |
5 | a0001c0001t0055g0068a0001c0001t0057g0103a0002c0002t0002g0060others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+80475_280+8048 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTCTCT others(5): Show |
6 | a0001c0001t0003g0144a0001c0001t0005g0146a0001c0001t0074g0142others(3): Show | 6 | HG02258.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+80473_280+8048 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTCTCT others(7): Show |
2 | a0001c0001t0001g0138a0002c0002t0002g0101 | 2 | HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+80471_280+8048 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
T | TTCTCTCT others(11): Show |
1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280+80467_280+8048 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
TTC | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(5): Show | 8 | HG00438.hp1 NA18952.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+80483_280+8048 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
TTCTC | T | 4 | a0001c0001t0001g0065a0001c0001t0009g0184a0001c0003t0029g0149others(1): Show | 4 | HG02615.hp2 HG02965.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+80481_280+8048 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
TTCTCTC | T | 82 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.280+80479_280+8048 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991818
|
TTCTCTCT others(1): Show |
T | 1 | a0005c0006t0003g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.280+80477_280+8048 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991818 | |||||
| chrX:71991848
|
C | CTCTG | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+80485_280+8048 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991848 | |||||
| chrX:71991848
|
C | G | 2 | a0001c0001t0005g0091a0001c0003t0033g0093 | 2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.280+80481C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71991848 | ||||||
| chrX:71991921
|
C | CA | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+80556dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71991921 | |||||
| chrX:71992036
|
A | G | 1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280+80669A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992036 | ||||||
| chrX:71992285
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+80918G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992285 | ||||||
| chrX:71992345
|
AG | A | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+80980delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71992345 | |||||
| chrX:71992364
|
T | TG | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+81001dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71992364 | |||||
| chrX:71992366
|
G | A | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0057g0103others(6): Show | 9 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+80999G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992366 | ||||||
| chrX:71992390
|
G | GA | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+81023_280+8102 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992390 | ||||||
| chrX:71992699
|
T | C | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+81332T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992699 | ||||||
| chrX:71992711
|
G | A | 1 | a0001c0003t0033g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.280+81344G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992711 | ||||||
| chrX:71992783
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 38 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.280+81416A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992783 | ||||||
| chrX:71992795
|
G | GA | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+81430dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71992795 | |||||
| chrX:71992966
|
C | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(34): Show | 37 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.280+81599C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992966 | ||||||
| chrX:71992983
|
A | AG | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.280+81619dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71992983 | |||||
| chrX:71992998
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0024g0001 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.280+81631C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71992998 | ||||||
| chrX:71993351
|
C | T | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+81984C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71993351 | ||||||
| chrX:71993523
|
G | A | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+82156G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71993523 | ||||||
| chrX:71993530
|
C | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(85): Show | 88 | HG00438.hp1 HG00738.hp1 HG01167.hp1 others(85): Show |
intron_variant | MODIFIER | c.280+82163C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71993530 | ||||||
| chrX:71993867
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.280+82500C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71993867 | ||||||
| chrX:71993867
|
C | CA | 2 | a0001c0001t0021g0007a0003c0004t0006g0083 | 2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.280+82514dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71993867 | |||||
| chrX:71993880
|
A | AT | 2 | a0001c0003t0012g0057a0001c0003t0012g0058 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.280+82513_280+8251 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71993880 | ||||||
| chrX:71993880
|
A | T | 13 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.280+82513A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71993880 | ||||||
| chrX:71994298
|
C | CTG | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.280+82961_280+8296 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTG | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0041others(9): Show | 12 | HG02040.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+82959_280+8296 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTG | 5 | a0001c0001t0051g0187a0002c0002t0002g0086a0002c0002t0002g0101others(2): Show | 5 | HG02886.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+82957_280+8296 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0037g0154a0002c0002t0002g0060a0002c0002t0002g0105 | 3 | HG02572.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280+82955_280+8296 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0057g0103a0001c0003t0035g0133 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.280+82953_280+8296 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280+82951_280+8296 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(7): Show |
20 | a0001c0001t0001g0074a0001c0001t0004g0066a0001c0001t0015g0135others(17): Show | 20 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+82949_280+8296 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(9): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0003t0011g0155others(3): Show | 6 | HG02976.hp1 HG03130.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+82947_280+8296 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(11): Show |
4 | a0001c0001t0019g0160a0001c0001t0019g0161a0001c0020t0005g0012others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+82945_280+8296 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(13): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0015g0049others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+82943_280+8296 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(15): Show |
2 | a0001c0003t0012g0057a0001c0003t0012g0058 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.280+82941_280+8296 others(26): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(17): Show |
1 | a0002c0002t0002g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.280+82939_280+8296 others(28): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
C | CTGTGTGT others(21): Show |
1 | a0001c0001t0023g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.280+82935_280+8296 others(32): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994298
|
CTGTGTGT others(3): Show |
C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+82953_280+8296 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71994298 | |||||
| chrX:71994391
|
C | T | 2 | a0001c0001t0004g0066a0002c0002t0002g0118 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.280+83024C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71994391 | ||||||
| chrX:71994410
|
T | C | 3 | a0001c0003t0011g0155a0001c0003t0011g0156a0002c0002t0002g0157 | 3 | HG02976.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280+83043T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71994410 | ||||||
| chrX:71994712
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+83345G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71994712 | ||||||
| chrX:71994762
|
G | A | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+83395G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71994762 | ||||||
| chrX:71994996
|
G | T | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+83629G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71994996 | ||||||
| chrX:71995379
|
C | G | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+84012C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71995379 | ||||||
| chrX:71995431
|
CTCTA | C | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.280+84068_280+8407 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71995431 | |||||
| chrX:71995597
|
G | A | 1 | a0008c0017t0053g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.280+84230G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71995597 | ||||||
| chrX:71995741
|
A | C | 1 | a0002c0002t0002g0145 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.280+84374A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71995741 | ||||||
| chrX:71995837
|
T | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.280+84470T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71995837 | ||||||
| chrX:71995972
|
A | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(89): Show | 92 | HG00438.hp1 HG00738.hp1 HG01167.hp1 others(89): Show |
intron_variant | MODIFIER | c.280+84605A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71995972 | ||||||
| chrX:71996110
|
C | G | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+84743C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71996110 | ||||||
| chrX:71996747
|
G | T | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+85380G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71996747 | ||||||
| chrX:71996987
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.280+85620C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71996987 | ||||||
| chrX:71997214
|
G | A | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+85847G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71997214 | ||||||
| chrX:71997800
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.280+86433T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71997800 | ||||||
| chrX:71997897
|
CACA | C | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.280+86535_280+8653 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71997897 | |||||
| chrX:71997914
|
TTTG | T | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+86553_280+8655 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71997914 | |||||
| chrX:71998003
|
CA | C | 1 | a0001c0001t0026g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.280+86638delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71998003 | |||||
| chrX:71998223
|
G | T | 15 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0019g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+86856G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71998223 | ||||||
| chrX:71998393
|
T | C | 1 | a0001c0001t0055g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.280+87026T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71998393 | ||||||
| chrX:71999329
|
T | C | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+87962T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71999329 | ||||||
| chrX:71999475
|
C | T | 1 | a0001c0001t0041g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.280+88108C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71999475 | ||||||
| chrX:71999794
|
TA | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(33): Show | 36 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.280+88436delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71999794 | |||||
| chrX:71999850
|
A | G | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+88483A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 71999850 | ||||||
| chrX:72000083
|
T | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(58): Show | 61 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(58): Show |
intron_variant | MODIFIER | c.280+88716T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72000083 | ||||||
| chrX:72000110
|
G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(24): Show | 27 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.280+88743G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72000110 | ||||||
| chrX:72000450
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.280+89083G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72000450 | ||||||
| chrX:72000568
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG00438.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.280+89201T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72000568 | ||||||
| chrX:72000694
|
C | A | 1 | a0002c0002t0013g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.280+89327C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72000694 | ||||||
| chrX:72000986
|
C | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(34): Show | 37 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.280+89619C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72000986 | ||||||
| chrX:72001215
|
A | G | 2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+89848A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72001215 | ||||||
| chrX:72001272
|
T | A | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280+89905T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72001272 | ||||||
| chrX:72001668
|
C | T | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(24): Show | 27 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.280+90301C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72001668 | ||||||
| chrX:72001772
|
A | G | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+90405A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72001772 | ||||||
| chrX:72002010
|
C | CT | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.280+90648dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72002010 | |||||
| chrX:72002125
|
A | G | 1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280+90758A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72002125 | ||||||
| chrX:72002150
|
C | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(24): Show | 27 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.280+90783C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72002150 | ||||||
| chrX:72002327
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 38 | HG00438.hp1 HG01243.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.280+90960A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72002327 | ||||||
| chrX:72002447
|
C | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(58): Show | 61 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(58): Show |
intron_variant | MODIFIER | c.280+91080C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72002447 | ||||||
| chrX:72002500
|
C | CT | 1 | a0001c0001t0022g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280+91134dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72002500 | |||||
| chrX:72002637
|
C | A | 3 | a0001c0001t0001g0170a0001c0001t0014g0173a0001c0001t0016g0175 | 3 | HG00642.hp1 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.280+91270C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72002637 | ||||||
| chrX:72002683
|
AC | A | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.280+91318delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72002683 | |||||
| chrX:72002923
|
A | AC | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.280+91559dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72002923 | |||||
| chrX:72003130
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+91763G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72003130 | ||||||
| chrX:72003297
|
A | T | 1 | a0002c0002t0002g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.280+91930A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72003297 | ||||||
| chrX:72003648
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.280+92281T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72003648 | ||||||
| chrX:72004431
|
T | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(24): Show | 27 | HG00738.hp1 HG01934.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.280+93064T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72004431 | ||||||
| chrX:72004723
|
G | A | 4 | a0001c0001t0005g0146a0001c0001t0037g0154a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02970.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+93356G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72004723 | ||||||
| chrX:72004993
|
G | A | 2 | a0001c0001t0004g0066a0002c0002t0002g0118 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.280+93626G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72004993 | ||||||
| chrX:72005237
|
C | G | 38 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(35): Show | 38 | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(35): Show |
intron_variant | MODIFIER | c.280+93870C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005237 | ||||||
| chrX:72005302
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.280+93935C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005302 | ||||||
| chrX:72005331
|
G | A | 2 | a0001c0001t0038g0158a0001c0003t0028g0159 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.280+93964G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005331 | ||||||
| chrX:72005440
|
G | A | 23 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0138others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.280+94073G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005440 | ||||||
| chrX:72005751
|
C | T | 3 | a0001c0001t0005g0091a0001c0003t0033g0093a0002c0002t0002g0145 | 3 | HG01109.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.280+94384C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005751 | ||||||
| chrX:72005766
|
T | G | 3 | a0001c0001t0001g0138a0001c0001t0056g0092a0009c0010t0052g0185 | 3 | HG02630.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+94399T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005766 | ||||||
| chrX:72005781
|
T | C | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280+94414T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72005781 | ||||||
| chrX:72006585
|
C | T | 17 | a0001c0001t0005g0096a0001c0001t0005g0146a0001c0001t0037g0154others(14): Show | 17 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+95218C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72006585 | ||||||
| chrX:72006622
|
G | A | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+95255G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72006622 | ||||||
| chrX:72007063
|
T | C | 19 | a0001c0001t0005g0096a0001c0001t0005g0146a0001c0001t0037g0154others(16): Show | 19 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.280+95696T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72007063 | ||||||
| chrX:72007155
|
G | A | 8 | a0001c0001t0037g0154a0001c0001t0051g0187a0002c0002t0002g0060others(5): Show | 8 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+95788G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72007155 | ||||||
| chrX:72007234
|
T | C | 1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280+95867T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72007234 | ||||||
| chrX:72007324
|
G | A | 1 | a0001c0001t0017g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.280+95957G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72007324 | ||||||
| chrX:72007448
|
C | G | 22 | a0001c0001t0001g0138a0001c0001t0005g0096a0001c0001t0005g0146others(19): Show | 22 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.280+96081C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72007448 | ||||||
| chrX:72007733
|
C | T | 7 | a0001c0001t0051g0187a0002c0002t0002g0060a0002c0002t0002g0086others(4): Show | 7 | HG02572.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.280+96366C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72007733 | ||||||
| chrX:72008149
|
C | T | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280+96782C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72008149 | ||||||
| chrX:72008559
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.280+97192C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72008559 | ||||||
| chrX:72008574
|
T | A | 1 | a0002c0002t0002g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.280+97207T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72008574 | ||||||
| chrX:72008575
|
G | T | 1 | a0002c0002t0002g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.280+97208G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72008575 | ||||||
| chrX:72008969
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.280+97602T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72008969 | ||||||
| chrX:72009056
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0056g0092a0009c0010t0052g0185 | 3 | HG02630.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+97689G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72009056 | ||||||
| chrX:72009157
|
A | G | 21 | a0001c0001t0001g0138a0001c0001t0005g0096a0001c0001t0005g0146others(18): Show | 21 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.280+97790A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72009157 | ||||||
| chrX:72009577
|
T | C | 1 | a0001c0001t0018g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.280+98210T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72009577 | ||||||
| chrX:72009702
|
C | A | 21 | a0001c0001t0001g0138a0001c0001t0005g0096a0001c0001t0005g0146others(18): Show | 21 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.280+98335C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72009702 | ||||||
| chrX:72009839
|
T | C | 11 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0001t0067g0148others(8): Show | 11 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+98472T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72009839 | ||||||
| chrX:72010032
|
C | T | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.280+98665C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010032 | ||||||
| chrX:72010086
|
C | T | 14 | a0001c0001t0001g0138a0001c0001t0037g0154a0001c0001t0051g0187others(11): Show | 14 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+98719C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010086 | ||||||
| chrX:72010388
|
G | T | 3 | a0001c0001t0001g0138a0001c0001t0056g0092a0009c0010t0052g0185 | 3 | HG02630.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+99021G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010388 | ||||||
| chrX:72010471
|
A | G | 1 | a0003c0004t0004g0186 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.280+99104A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010471 | ||||||
| chrX:72010478
|
C | T | 21 | a0001c0001t0001g0138a0001c0001t0005g0096a0001c0001t0005g0146others(18): Show | 21 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.280+99111C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010478 | ||||||
| chrX:72010605
|
C | G | 1 | a0001c0003t0031g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280+99238C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010605 | ||||||
| chrX:72010824
|
A | G | 1 | a0001c0003t0029g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.280+99457A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010824 | ||||||
| chrX:72010956
|
G | A | 2 | a0001c0001t0022g0052a0001c0003t0036g0054 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.280+99589G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72010956 | ||||||
| chrX:72011151
|
C | T | 1 | a0001c0001t0047g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.280+99784C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011151 | ||||||
| chrX:72011172
|
G | A | 1 | a0001c0012t0003g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.280+99805G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011172 | ||||||
| chrX:72011418
|
TC | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+100054delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72011418 | |||||
| chrX:72011442
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.280+100075T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011442 | ||||||
| chrX:72011453
|
C | T | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+100086C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011453 | ||||||
| chrX:72011567
|
G | A | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280+100200G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011567 | ||||||
| chrX:72011669
|
C | CA | 2 | a0001c0001t0062g0036a0002c0002t0002g0105 | 2 | HG02572.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.280+100312dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72011669 | |||||
| chrX:72011818
|
G | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+100451G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011818 | ||||||
| chrX:72011908
|
T | C | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280+100541T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011908 | ||||||
| chrX:72011927
|
T | A | 4 | a0001c0001t0005g0096a0001c0001t0005g0146a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+100560T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72011927 | ||||||
| chrX:72011998
|
CT | C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+100634delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72011998 | |||||
| chrX:72012216
|
TC | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+100851delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72012216 | |||||
| chrX:72012275
|
A | AT | 2 | a0001c0003t0028g0159a0001c0003t0070g0027 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280+100918dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72012275 | |||||
| chrX:72012308
|
T | C | 5 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0014t0040g0167others(2): Show | 5 | HG01169.hp2 HG01256.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+100941T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72012308 | ||||||
| chrX:72012368
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.280+101001A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72012368 | ||||||
| chrX:72012430
|
TC | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+101066delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72012430 | |||||
| chrX:72012659
|
ATAAGG | A | 1 | a0001c0001t0083g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280+101296_280+101 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72012659 | |||||
| chrX:72012699
|
C | T | 1 | a0002c0002t0002g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280+101332C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72012699 | ||||||
| chrX:72012711
|
G | C | 1 | a0001c0001t0001g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.280+101344G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72012711 | ||||||
| chrX:72012748
|
AT | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+101387delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72012748 | |||||
| chrX:72013019
|
A | G | 2 | a0002c0002t0077g0183a0002c0002t0079g0165 | 2 | NA18989.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.280+101652A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72013019 | ||||||
| chrX:72013244
|
G | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.280+101877G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72013244 | ||||||
| chrX:72013536
|
C | CT | 9 | a0001c0001t0001g0018a0001c0001t0057g0103a0001c0001t0067g0148others(6): Show | 9 | HG02109.hp2 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+102182dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72013536 | |||||
| chrX:72013536
|
C | CTT | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280+102181_280+102 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72013536 | |||||
| chrX:72013536
|
C | CTTT | 2 | a0001c0001t0001g0138a0001c0001t0056g0092 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.280+102180_280+102 others(9): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72013536 | |||||
| chrX:72013536
|
CT | C | 3 | a0001c0001t0001g0094a0002c0002t0002g0095a0010c0016t0075g0137 | 3 | HG02145.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.280+102182delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72013536 | |||||
| chrX:72013594
|
G | GA | 4 | a0001c0001t0067g0148a0001c0003t0028g0159a0001c0003t0029g0149others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+102227_280+102 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72013594 | ||||||
| chrX:72013704
|
A | G | 11 | a0001c0001t0001g0138a0001c0001t0056g0092a0001c0001t0057g0103others(8): Show | 11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+102337A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72013704 | ||||||
| chrX:72013785
|
G | GT | 1 | a0001c0001t0022g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280+102426dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72013785 | |||||
| chrX:72013959
|
AG | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+102595delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72013959 | |||||
| chrX:72014063
|
G | C | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+102696G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72014063 | ||||||
| chrX:72014407
|
T | C | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.280+103040T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72014407 | ||||||
| chrX:72014420
|
TG | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+103055delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72014420 | |||||
| chrX:72014500
|
G | A | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+103133G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72014500 | ||||||
| chrX:72014503
|
C | A | 1 | a0001c0012t0003g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.280+103136C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72014503 | ||||||
| chrX:72014783
|
CA | C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+103419delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72014783 | |||||
| chrX:72014788
|
CA | C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+103424delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72014788 | |||||
| chrX:72014844
|
A | G | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280+103477A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72014844 | ||||||
| chrX:72014857
|
A | G | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+103490A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72014857 | ||||||
| chrX:72014954
|
AC | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+103591delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72014954 | |||||
| chrX:72015065
|
TA | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+103704delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72015065 | |||||
| chrX:72015167
|
C | T | 2 | a0001c0001t0004g0128a0002c0002t0007g0129 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.280+103800C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72015167 | ||||||
| chrX:72015314
|
TC | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+103950delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72015314 | |||||
| chrX:72015366
|
A | G | 7 | a0001c0001t0001g0098a0001c0001t0010g0084a0001c0001t0022g0127others(4): Show | 7 | HG00673.hp1 NA18747.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+103999A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72015366 | ||||||
| chrX:72015540
|
AG | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+104177delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72015540 | |||||
| chrX:72015679
|
GA | G | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+104314delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72015679 | |||||
| chrX:72015804
|
C | T | 1 | a0001c0011t0003g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280+104437C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72015804 | ||||||
| chrX:72015876
|
T | G | 22 | a0001c0001t0001g0138a0001c0001t0005g0096a0001c0001t0005g0146others(19): Show | 22 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.280+104509T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72015876 | ||||||
| chrX:72016062
|
AC | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+104697delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016062 | |||||
| chrX:72016114
|
CT | C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+104753delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016114 | |||||
| chrX:72016154
|
T | C | 11 | a0001c0001t0001g0138a0001c0001t0056g0092a0001c0001t0057g0103others(8): Show | 11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+104787T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72016154 | ||||||
| chrX:72016185
|
AT | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+104823delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016185 | |||||
| chrX:72016363
|
G | T | 1 | a0001c0001t0080g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.280+104996G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72016363 | ||||||
| chrX:72016480
|
GT | G | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+105116delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016480 | |||||
| chrX:72016568
|
CT | C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+105205delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016568 | |||||
| chrX:72016618
|
C | A | 1 | a0001c0001t0073g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280+105251C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72016618 | ||||||
| chrX:72016661
|
A | AAC | 9 | a0001c0001t0015g0135a0001c0001t0037g0154a0001c0001t0051g0187others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+105308_280+105 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016661 | |||||
| chrX:72016675
|
CA | C | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+105311delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016675 | |||||
| chrX:72016687
|
C | G | 3 | a0001c0001t0019g0160a0001c0001t0019g0161a0002c0002t0002g0086 | 3 | HG01167.hp1 HG01169.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.280+105320C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72016687 | ||||||
| chrX:72016750
|
A | G | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+105383A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72016750 | ||||||
| chrX:72016767
|
AG | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+105402delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016767 | |||||
| chrX:72016849
|
AC | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+105485delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72016849 | |||||
| chrX:72016897
|
A | G | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+105530A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72016897 | ||||||
| chrX:72017290
|
C | T | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+105923C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72017290 | ||||||
| chrX:72017410
|
TG | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106045delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72017410 | |||||
| chrX:72017460
|
TC | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106095delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72017460 | |||||
| chrX:72017482
|
A | G | 4 | a0001c0001t0001g0028a0001c0019t0054g0070a0001c0020t0005g0012others(1): Show | 4 | HG00738.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+106115A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72017482 | ||||||
| chrX:72017595
|
TG | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106231delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72017595 | |||||
| chrX:72017648
|
A | C | 7 | a0001c0001t0001g0138a0001c0001t0056g0092a0001c0001t0067g0148others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+106281A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72017648 | ||||||
| chrX:72017722
|
A | C | 1 | a0001c0001t0074g0142 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.280+106355A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72017722 | ||||||
| chrX:72017827
|
AT | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106464delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72017827 | |||||
| chrX:72017993
|
C | T | 3 | a0001c0001t0005g0146a0001c0001t0074g0142a0002c0002t0002g0143 | 3 | HG02258.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.280+106626C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72017993 | ||||||
| chrX:72018121
|
AAT | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106755_280+106 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018121 | ||||||
| chrX:72018124
|
G | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106757G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018124 | ||||||
| chrX:72018158
|
A | T | 4 | a0001c0001t0067g0148a0001c0003t0028g0159a0001c0003t0029g0149others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+106791A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018158 | ||||||
| chrX:72018177
|
AC | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+106812delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72018177 | |||||
| chrX:72018210
|
A | G | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+106843A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018210 | ||||||
| chrX:72018260
|
T | C | 4 | a0001c0001t0067g0148a0001c0003t0028g0159a0001c0003t0029g0149others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+106893T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018260 | ||||||
| chrX:72018381
|
T | TA | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+107019dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72018381 | |||||
| chrX:72018423
|
C | CG | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+107057dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72018423 | |||||
| chrX:72018427
|
A | G | 2 | a0001c0001t0009g0032a0001c0001t0020g0139 | 2 | NA18994.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.280+107060A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018427 | ||||||
| chrX:72018471
|
C | G | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+107104C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018471 | ||||||
| chrX:72018721
|
C | T | 2 | a0001c0001t0004g0128a0002c0002t0007g0129 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.280+107354C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018721 | ||||||
| chrX:72018805
|
T | C | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+107438T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018805 | ||||||
| chrX:72018859
|
A | G | 5 | a0002c0002t0002g0060a0002c0002t0002g0101a0002c0002t0002g0104others(2): Show | 5 | HG02572.hp1 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+107492A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018859 | ||||||
| chrX:72018937
|
T | C | 2 | a0001c0001t0021g0006a0001c0001t0021g0007 | 2 | NA18952.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.280+107570T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72018937 | ||||||
| chrX:72019344
|
AG | A | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+107980delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72019344 | |||||
| chrX:72019368
|
G | C | 2 | a0001c0001t0046g0123a0007c0008t0001g0110 | 2 | HG01258.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.280+108001G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72019368 | ||||||
| chrX:72019836
|
A | G | 1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280+108469A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72019836 | ||||||
| chrX:72020007
|
T | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.280+108640T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72020007 | ||||||
| chrX:72020035
|
C | T | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280+108668C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72020035 | ||||||
| chrX:72020261
|
C | T | 1 | a0007c0008t0001g0110 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.280+108894C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72020261 | ||||||
| chrX:72020363
|
TG | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.280+108999delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72020363 | |||||
| chrX:72020772
|
A | G | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+109405A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72020772 | ||||||
| chrX:72020792
|
T | A | 26 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0072others(23): Show | 26 | HG00621.hp1 HG00738.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.280+109425T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72020792 | ||||||
| chrX:72021032
|
G | A | 1 | a0001c0001t0045g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.280+109665G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72021032 | ||||||
| chrX:72021060
|
TAC | T | 44 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0035others(41): Show | 44 | HG00621.hp1 HG00738.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.280+109721_280+109 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72021060 | |||||
| chrX:72021060
|
TACAC | T | 7 | a0001c0001t0005g0096a0001c0001t0005g0146a0001c0001t0057g0103others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+109719_280+109 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72021060 | |||||
| chrX:72021060
|
TACACAC | T | 8 | a0001c0001t0037g0154a0001c0001t0051g0187a0001c0003t0033g0093others(5): Show | 8 | HG02572.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+109717_280+109 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72021060 | |||||
| chrX:72021060
|
TACACACA others(3): Show |
T | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280+109713_280+109 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72021060 | |||||
| chrX:72021060
|
TACACACA others(5): Show |
T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.280+109711_280+109 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72021060 | |||||
| chrX:72021060
|
TACACACA others(11): Show |
T | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280+109705_280+109 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72021060 | |||||
| chrX:72021597
|
A | C | 1 | a0001c0003t0012g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.280+110230A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72021597 | ||||||
| chrX:72021808
|
G | A | 1 | a0004c0005t0043g0061 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.281-110271G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72021808 | ||||||
| chrX:72022029
|
G | C | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.281-110050G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72022029 | ||||||
| chrX:72022315
|
T | C | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-109764T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72022315 | ||||||
| chrX:72022410
|
A | AT | 1 | a0001c0013t0003g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.281-109659dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72022410 | |||||
| chrX:72022410
|
AT | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | NA18944.hp1 NA18961.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-109659delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72022410 | |||||
| chrX:72022990
|
G | T | 1 | a0001c0001t0004g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.281-109089G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72022990 | ||||||
| chrX:72023260
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.281-108819C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72023260 | ||||||
| chrX:72023684
|
G | C | 1 | a0001c0001t0083g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.281-108395G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72023684 | ||||||
| chrX:72023750
|
C | T | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-108329C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72023750 | ||||||
| chrX:72024419
|
C | T | 3 | a0001c0003t0011g0155a0001c0003t0011g0156a0002c0002t0002g0157 | 3 | HG02976.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.281-107660C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72024419 | ||||||
| chrX:72024462
|
C | T | 1 | a0001c0001t0039g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.281-107617C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72024462 | ||||||
| chrX:72024568
|
G | A | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-107511G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72024568 | ||||||
| chrX:72024584
|
AG | A | 1 | a0001c0011t0003g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.281-107494delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72024584 | ||||||
| chrX:72024643
|
G | A | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.281-107436G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72024643 | ||||||
| chrX:72024951
|
A | G | 1 | a0003c0004t0063g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.281-107128A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72024951 | ||||||
| chrX:72025196
|
G | A | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-106883G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025196 | ||||||
| chrX:72025302
|
G | A | 2 | a0001c0001t0067g0148a0001c0003t0029g0149 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.281-106777G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025302 | ||||||
| chrX:72025413
|
A | G | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.281-106666A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025413 | ||||||
| chrX:72025506
|
T | C | 3 | a0001c0001t0067g0148a0001c0003t0029g0149a0001c0003t0084g0150 | 3 | HG02109.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.281-106573T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025506 | ||||||
| chrX:72025533
|
G | A | 7 | a0001c0001t0001g0098a0001c0001t0010g0084a0001c0001t0022g0127others(4): Show | 7 | HG00673.hp1 NA18747.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-106546G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025533 | ||||||
| chrX:72025739
|
G | GGA | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-106339_281-106 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72025739 | |||||
| chrX:72025907
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-106172G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025907 | ||||||
| chrX:72025975
|
G | A | 2 | a0001c0001t0010g0008a0001c0001t0064g0009 | 2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.281-106104G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025975 | ||||||
| chrX:72025991
|
A | G | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-106088A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72025991 | ||||||
| chrX:72026089
|
CT | C | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-105987delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72026089 | |||||
| chrX:72026241
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0177others(6): Show | 9 | HG01169.hp2 HG01256.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-105838G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72026241 | ||||||
| chrX:72026411
|
G | A | 2 | a0001c0001t0003g0016a0001c0001t0016g0175 | 2 | HG00642.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.281-105668G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72026411 | ||||||
| chrX:72026488
|
TG | T | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-105588delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72026488 | |||||
| chrX:72026815
|
C | T | 1 | a0001c0001t0083g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.281-105264C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72026815 | ||||||
| chrX:72026862
|
CTG | C | 1 | a0001c0003t0011g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-105215_281-105 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72026862 | |||||
| chrX:72026978
|
T | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.281-105101T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72026978 | ||||||
| chrX:72027106
|
C | G | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-104973C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72027106 | ||||||
| chrX:72027200
|
C | G | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-104879C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72027200 | ||||||
| chrX:72027357
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-104722G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72027357 | ||||||
| chrX:72027420
|
G | A | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-104659G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72027420 | ||||||
| chrX:72027432
|
C | T | 1 | a0008c0017t0053g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281-104647C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72027432 | ||||||
| chrX:72028169
|
A | G | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0002c0002t0002g0060others(6): Show | 9 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-103910A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72028169 | ||||||
| chrX:72028431
|
T | A | 1 | a0006c0007t0013g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.281-103648T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72028431 | ||||||
| chrX:72029051
|
G | A | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-103028G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72029051 | ||||||
| chrX:72029168
|
TG | T | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-102907delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72029168 | |||||
| chrX:72029391
|
A | G | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-102688A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72029391 | ||||||
| chrX:72029448
|
A | G | 1 | a0003c0004t0006g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.281-102631A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72029448 | ||||||
| chrX:72029452
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-102627G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72029452 | ||||||
| chrX:72029699
|
C | T | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-102380C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72029699 | ||||||
| chrX:72029882
|
A | T | 1 | a0001c0001t0004g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.281-102197A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72029882 | ||||||
| chrX:72030363
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281-101716C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72030363 | ||||||
| chrX:72030368
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.281-101711G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72030368 | ||||||
| chrX:72030496
|
A | ATG | 7 | a0001c0001t0001g0041a0001c0001t0005g0096a0001c0001t0014g0173others(4): Show | 7 | HG02040.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-101565_281-101 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72030496 | |||||
| chrX:72030496
|
A | ATGTG | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-101567_281-101 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72030496 | |||||
| chrX:72030549
|
A | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.281-101530A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72030549 | ||||||
| chrX:72030626
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281-101453A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72030626 | ||||||
| chrX:72030743
|
A | G | 25 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-101336A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72030743 | ||||||
| chrX:72031005
|
G | A | 19 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(16): Show | 19 | HG02129.hp1 HG02523.hp1 NA18943.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-101074G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031005 | ||||||
| chrX:72031108
|
C | T | 9 | a0001c0001t0037g0154a0001c0001t0051g0187a0002c0002t0002g0060others(6): Show | 9 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-100971C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031108 | ||||||
| chrX:72031263
|
G | A | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.281-100816G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031263 | ||||||
| chrX:72031289
|
C | T | 1 | a0001c0013t0003g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.281-100790C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031289 | ||||||
| chrX:72031430
|
A | G | 1 | a0001c0001t0004g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.281-100649A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031430 | ||||||
| chrX:72031578
|
A | G | 1 | a0002c0002t0007g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.281-100501A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031578 | ||||||
| chrX:72031736
|
G | GA | 14 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0010g0084others(11): Show | 14 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-100325dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72031736 | |||||
| chrX:72031736
|
GA | G | 1 | a0002c0002t0079g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.281-100325delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72031736 | |||||
| chrX:72031851
|
C | CA | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-100221dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72031851 | |||||
| chrX:72031972
|
C | T | 5 | a0001c0001t0001g0138a0001c0001t0019g0160a0001c0001t0019g0161others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-100107C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72031972 | ||||||
| chrX:72032089
|
TA | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.281-99972delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72032089 | |||||
| chrX:72032089
|
TAA | T | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-99973_281-9997 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72032089 | |||||
| chrX:72032102
|
A | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.281-99977A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032102 | ||||||
| chrX:72032105
|
A | AT | 3 | a0001c0001t0001g0138a0001c0001t0056g0092a0001c0003t0033g0093 | 3 | HG02818.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.281-99974_281-9997 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032105 | ||||||
| chrX:72032105
|
A | T | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.281-99974A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032105 | ||||||
| chrX:72032117
|
C | A | 1 | a0007c0008t0001g0110 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.281-99962C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032117 | ||||||
| chrX:72032118
|
G | A | 1 | a0006c0007t0013g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.281-99961G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032118 | ||||||
| chrX:72032285
|
C | T | 1 | a0001c0003t0012g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-99794C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032285 | ||||||
| chrX:72032318
|
C | T | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-99761C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032318 | ||||||
| chrX:72032325
|
C | T | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-99754C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032325 | ||||||
| chrX:72032387
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-99692C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032387 | ||||||
| chrX:72032488
|
A | G | 4 | a0001c0001t0005g0096a0001c0001t0057g0103a0008c0017t0053g0059others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-99591A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032488 | ||||||
| chrX:72032781
|
C | T | 1 | a0002c0002t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.281-99298C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032781 | ||||||
| chrX:72032824
|
A | T | 1 | a0003c0004t0008g0003 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.281-99255A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032824 | ||||||
| chrX:72032998
|
A | G | 1 | a0001c0001t0017g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.281-99081A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72032998 | ||||||
| chrX:72033073
|
CT | C | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-99003delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72033073 | |||||
| chrX:72033183
|
C | CT | 61 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0045others(58): Show | 61 | HG00621.hp1 HG00738.hp1 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.281-98876dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72033183 | |||||
| chrX:72033183
|
C | CTT | 2 | a0001c0001t0005g0091a0001c0003t0084g0150 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.281-98877_281-9887 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72033183 | |||||
| chrX:72033183
|
C | CTTT | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-98878_281-9887 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72033183 | |||||
| chrX:72033183
|
CT | C | 4 | a0001c0001t0001g0108a0001c0001t0049g0019a0001c0003t0028g0159others(1): Show | 4 | HG02257.hp1 HG03225.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-98876delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72033183 | |||||
| chrX:72033187
|
T | C | 2 | a0001c0001t0010g0008a0001c0001t0064g0009 | 2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.281-98892T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72033187 | ||||||
| chrX:72033312
|
A | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.281-98767A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72033312 | ||||||
| chrX:72033375
|
T | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.281-98704T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72033375 | ||||||
| chrX:72033461
|
AG | A | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-98616delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72033461 | |||||
| chrX:72033475
|
G | T | 15 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0015g0049others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-98604G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72033475 | ||||||
| chrX:72033525
|
C | T | 25 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-98554C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72033525 | ||||||
| chrX:72033991
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281-98088C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72033991 | ||||||
| chrX:72034230
|
A | G | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-97849A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72034230 | ||||||
| chrX:72034341
|
TA | T | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-97734delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72034341 | |||||
| chrX:72034532
|
T | C | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0005c0006t0003g0180others(1): Show | 4 | HG01169.hp2 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-97547T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72034532 | ||||||
| chrX:72034578
|
T | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.281-97501T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72034578 | ||||||
| chrX:72034658
|
G | GT | 1 | a0001c0001t0049g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.281-97418dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72034658 | |||||
| chrX:72034805
|
TTTTATC | T | 1 | a0002c0002t0002g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.281-97270_281-9726 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72034805 | |||||
| chrX:72034877
|
G | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.281-97202G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72034877 | ||||||
| chrX:72035014
|
T | C | 15 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0015g0049others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-97065T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72035014 | ||||||
| chrX:72035158
|
A | G | 1 | a0002c0002t0076g0075 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.281-96921A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72035158 | ||||||
| chrX:72035260
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-96819C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72035260 | ||||||
| chrX:72035355
|
C | CT | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.281-96721dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72035355 | |||||
| chrX:72035363
|
A | G | 2 | a0001c0001t0015g0135a0001c0001t0073g0134 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.281-96716A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72035363 | ||||||
| chrX:72035476
|
A | G | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-96603A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72035476 | ||||||
| chrX:72036214
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-95865G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72036214 | ||||||
| chrX:72036223
|
G | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.281-95856G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72036223 | ||||||
| chrX:72036234
|
C | G | 2 | a0001c0001t0046g0123a0007c0008t0001g0110 | 2 | HG01258.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.281-95845C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72036234 | ||||||
| chrX:72036307
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.281-95772G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72036307 | ||||||
| chrX:72036444
|
A | G | 1 | a0001c0001t0064g0009 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.281-95635A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72036444 | ||||||
| chrX:72036468
|
C | T | 10 | a0001c0001t0001g0053a0001c0001t0001g0065a0001c0001t0015g0049others(7): Show | 10 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.281-95611C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72036468 | ||||||
| chrX:72037157
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281-94922C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72037157 | ||||||
| chrX:72037348
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-94731G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72037348 | ||||||
| chrX:72037422
|
C | CA | 1 | a0002c0002t0002g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.281-94647dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72037422 | |||||
| chrX:72037433
|
GAAA | G | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.281-94639_281-9463 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72037433 | |||||
| chrX:72037545
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.281-94534G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72037545 | ||||||
| chrX:72037618
|
G | T | 1 | a0002c0002t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.281-94461G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72037618 | ||||||
| chrX:72037655
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.281-94424A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72037655 | ||||||
| chrX:72037973
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0024g0001 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.281-94106C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72037973 | ||||||
| chrX:72038042
|
A | G | 1 | a0001c0003t0036g0054 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.281-94037A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72038042 | ||||||
| chrX:72038079
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.281-94000C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72038079 | ||||||
| chrX:72038119
|
A | G | 3 | a0001c0001t0005g0096a0001c0001t0057g0103a0008c0017t0053g0059 | 3 | HG02280.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.281-93960A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72038119 | ||||||
| chrX:72038267
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-93812A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72038267 | ||||||
| chrX:72038864
|
T | C | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-93215T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72038864 | ||||||
| chrX:72038888
|
G | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-93191G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72038888 | ||||||
| chrX:72039007
|
A | AG | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-93070dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039007 | |||||
| chrX:72039062
|
T | TTTTCCTT others(8): Show |
1 | a0001c0001t0001g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.281-93013_281-9301 others(19): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039062 | |||||
| chrX:72039067
|
T | C | 1 | a0001c0001t0001g0034 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.281-93012T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72039067 | ||||||
| chrX:72039067
|
T | TTTTCC | 20 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0022others(17): Show | 20 | HG01099.hp1 HG02559.hp1 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.281-92934_281-9293 others(9): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(3): Show |
25 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0047others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-92939_281-9293 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(8): Show |
19 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG00642.hp1 HG01515.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-92944_281-9293 others(19): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(13): Show |
18 | a0001c0001t0001g0026a0001c0001t0001g0098a0001c0001t0001g0126others(15): Show | 18 | HG01074.hp1 HG01106.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-92949_281-9293 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(18): Show |
13 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0014g0125others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.281-92954_281-9293 others(29): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(23): Show |
2 | a0001c0001t0001g0170a0001c0001t0009g0184 | 2 | HG01433.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.281-92959_281-9293 others(34): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(28): Show |
1 | a0001c0001t0041g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.281-92964_281-9293 others(39): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
T | TTTTCCTT others(33): Show |
1 | a0001c0001t0047g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281-92969_281-9293 others(44): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCC | T | 18 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0035others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-92934_281-9293 others(9): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCCTT others(3): Show |
T | 19 | a0001c0001t0001g0074a0001c0001t0005g0091a0001c0001t0015g0135others(16): Show | 19 | HG00738.hp1 HG01109.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-92939_281-9293 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCCTT others(8): Show |
T | 11 | a0001c0001t0001g0072a0001c0001t0001g0138a0001c0001t0004g0066others(8): Show | 11 | HG00673.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.281-92944_281-9293 others(19): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCCTT others(13): Show |
T | 4 | a0001c0001t0037g0154a0001c0001t0038g0158a0001c0001t0051g0187others(1): Show | 4 | HG02451.hp1 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-92949_281-9293 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCCTT others(18): Show |
T | 3 | a0001c0003t0031g0140a0001c0003t0036g0054a0002c0002t0002g0086 | 3 | HG02896.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.281-92954_281-9293 others(29): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCCTT others(23): Show |
T | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-92959_281-9293 others(34): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039067
|
TTTTCCTT others(28): Show |
T | 1 | a0002c0002t0002g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.281-92964_281-9293 others(39): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039067 | |||||
| chrX:72039127
|
C | CTTTCCTT others(9): Show |
1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.281-92949_281-9293 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039127 | |||||
| chrX:72039130
|
TCCTTTCC others(13): Show |
T | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-92947_281-9292 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72039130 | |||||
| chrX:72039185
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281-92894G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72039185 | ||||||
| chrX:72039251
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.281-92828C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72039251 | ||||||
| chrX:72039314
|
C | T | 3 | a0001c0001t0005g0091a0001c0003t0031g0140a0002c0002t0002g0141 | 3 | HG01109.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.281-92765C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72039314 | ||||||
| chrX:72039535
|
G | A | 4 | a0001c0001t0005g0146a0001c0001t0074g0142a0002c0002t0002g0086others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-92544G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72039535 | ||||||
| chrX:72039662
|
C | G | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-92417C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72039662 | ||||||
| chrX:72040013
|
A | G | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-92066A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72040013 | ||||||
| chrX:72040144
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | NA18944.hp1 NA18959.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-91935G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72040144 | ||||||
| chrX:72040300
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0021g0006a0001c0001t0021g0007 | 3 | NA18952.hp1 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.281-91779C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72040300 | ||||||
| chrX:72040324
|
C | G | 16 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0015g0049others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-91755C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72040324 | ||||||
| chrX:72040447
|
A | AT | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-91625dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72040447 | |||||
| chrX:72040479
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0045g0174 | 2 | HG02083.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.281-91600G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72040479 | ||||||
| chrX:72040954
|
A | G | 1 | a0001c0001t0020g0139 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.281-91125A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72040954 | ||||||
| chrX:72041093
|
T | C | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-90986T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72041093 | ||||||
| chrX:72041306
|
G | A | 2 | a0001c0003t0012g0057a0001c0003t0012g0058 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.281-90773G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72041306 | ||||||
| chrX:72041805
|
C | T | 1 | a0001c0012t0003g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.281-90274C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72041805 | ||||||
| chrX:72042224
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-89855G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72042224 | ||||||
| chrX:72042377
|
G | A | 1 | a0001c0001t0083g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.281-89702G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72042377 | ||||||
| chrX:72042407
|
T | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.281-89672T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72042407 | ||||||
| chrX:72042568
|
A | G | 1 | a0001c0001t0025g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.281-89511A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72042568 | ||||||
| chrX:72042573
|
C | G | 6 | a0001c0001t0001g0028a0001c0001t0055g0068a0001c0015t0032g0031others(3): Show | 6 | HG00738.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-89506C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72042573 | ||||||
| chrX:72042754
|
C | CA | 3 | a0001c0001t0018g0076a0006c0007t0013g0090a0010c0016t0075g0137 | 3 | HG02055.hp1 HG02257.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.281-89310dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72042754 | |||||
| chrX:72042754
|
CA | C | 2 | a0001c0001t0001g0170a0001c0003t0084g0150 | 2 | HG01433.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.281-89310delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72042754 | |||||
| chrX:72042754
|
CAA | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.281-89311_281-8931 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72042754 | |||||
| chrX:72042754
|
CAAA | C | 1 | a0001c0001t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.281-89312_281-8931 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72042754 | |||||
| chrX:72042845
|
C | T | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-89234C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72042845 | ||||||
| chrX:72043943
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.281-88136T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72043943 | ||||||
| chrX:72043981
|
T | C | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-88098T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72043981 | ||||||
| chrX:72044627
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0067g0148a0001c0003t0029g0149 | 3 | HG02109.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.281-87452G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72044627 | ||||||
| chrX:72044933
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.281-87146G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72044933 | ||||||
| chrX:72044959
|
T | TA | 2 | a0004c0005t0043g0061a0005c0006t0058g0079 | 2 | HG01934.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.281-87105dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72044959 | |||||
| chrX:72044959
|
TA | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0033others(2): Show | 5 | HG00738.hp1 NA18948.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-87105delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72044959 | |||||
| chrX:72045131
|
C | T | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-86948C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72045131 | ||||||
| chrX:72045514
|
G | A | 4 | a0001c0001t0001g0028a0001c0019t0054g0070a0001c0020t0005g0012others(1): Show | 4 | HG00738.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-86565G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72045514 | ||||||
| chrX:72045614
|
A | G | 1 | a0002c0002t0002g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.281-86465A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72045614 | ||||||
| chrX:72045814
|
A | G | 1 | a0003c0004t0004g0186 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.281-86265A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72045814 | ||||||
| chrX:72046113
|
A | T | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-85966A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72046113 | ||||||
| chrX:72046177
|
G | A | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-85902G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72046177 | ||||||
| chrX:72046590
|
A | AAAGTTGA others(27): Show |
1 | a0001c0001t0009g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.281-85487_281-8545 others(38): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72046590 | |||||
| chrX:72047005
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-85074G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72047005 | ||||||
| chrX:72047370
|
C | T | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-84709C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72047370 | ||||||
| chrX:72047451
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.281-84628G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72047451 | ||||||
| chrX:72047765
|
G | C | 2 | a0001c0003t0028g0159a0001c0003t0084g0150 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.281-84314G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72047765 | ||||||
| chrX:72048064
|
C | CATG | 2 | a0001c0001t0005g0146a0001c0001t0074g0142 | 2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.281-84009_281-8400 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048064 | |||||
| chrX:72048070
|
G | GATA | 3 | a0001c0001t0005g0096a0001c0003t0029g0149a0002c0002t0002g0060 | 3 | HG02280.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.281-84007_281-8400 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048070 | |||||
| chrX:72048070
|
G | GATGATA | 1 | a0002c0002t0002g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.281-84007_281-8400 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048070 | |||||
| chrX:72048070
|
G | GATGATAA others(2): Show |
1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-84007_281-8400 others(13): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048070 | |||||
| chrX:72048070
|
GATAACA | G | 22 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0094others(19): Show | 22 | HG00140.hp1 HG01074.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-84004_281-8399 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048070 | |||||
| chrX:72048070
|
GATAACAA others(2): Show |
G | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(107): Show | 110 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.281-84004_281-8399 others(13): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048070 | |||||
| chrX:72048070
|
GATAACAA others(5): Show |
G | 29 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(26): Show | 29 | HG00673.hp1 HG02056.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.281-84004_281-8399 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048070 | |||||
| chrX:72048072
|
TAAC | T | 4 | a0001c0001t0056g0092a0001c0001t0057g0103a0008c0017t0053g0059others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-84004_281-8400 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048072 | |||||
| chrX:72048075
|
C | T | 22 | a0001c0001t0001g0030a0001c0001t0005g0096a0001c0001t0005g0146others(19): Show | 22 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-84004C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048075 | ||||||
| chrX:72048082
|
A | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(24): Show | 27 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-83997A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048082 | ||||||
| chrX:72048085
|
A | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(24): Show | 27 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-83994A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048085 | ||||||
| chrX:72048088
|
A | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-83991A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048088 | ||||||
| chrX:72048324
|
T | G | 2 | a0001c0001t0001g0030a0006c0007t0013g0090 | 2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.281-83755T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048324 | ||||||
| chrX:72048344
|
C | A | 3 | a0001c0003t0011g0155a0001c0003t0011g0156a0002c0002t0002g0157 | 3 | HG02976.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.281-83735C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048344 | ||||||
| chrX:72048456
|
C | T | 1 | a0001c0015t0032g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.281-83623C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048456 | ||||||
| chrX:72048583
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281-83496C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048583 | ||||||
| chrX:72048683
|
C | A | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-83396C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048683 | ||||||
| chrX:72048790
|
C | T | 27 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(24): Show | 27 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-83289C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72048790 | ||||||
| chrX:72048812
|
CAG | C | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-83264_281-8326 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048812 | |||||
| chrX:72048987
|
G | GAGAAGAA others(11): Show |
2 | a0001c0001t0001g0074a0001c0003t0036g0054 | 2 | HG06807.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.281-83082_281-8306 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(14): Show |
2 | a0001c0001t0005g0091a0001c0001t0005g0096 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.281-83085_281-8306 others(25): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(17): Show |
6 | a0001c0001t0001g0047a0001c0001t0004g0066a0001c0001t0022g0052others(3): Show | 6 | HG02083.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-83088_281-8306 others(28): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(20): Show |
3 | a0001c0003t0031g0140a0003c0004t0008g0071a0004c0005t0082g0062 | 3 | NA19043.hp1 NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.281-83091_281-8306 others(31): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(23): Show |
9 | a0001c0001t0001g0035a0001c0001t0005g0146a0001c0001t0015g0135others(6): Show | 9 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-83065_281-8306 others(34): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(26): Show |
4 | a0001c0001t0001g0072a0001c0001t0045g0174a0001c0001t0080g0073others(1): Show | 4 | HG01358.hp1 HG03688.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-83065_281-8306 others(37): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(29): Show |
4 | a0001c0001t0018g0076a0001c0001t0038g0158a0001c0003t0028g0159others(1): Show | 4 | HG02451.hp1 HG03225.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-83065_281-8306 others(40): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(32): Show |
2 | a0002c0002t0002g0141a0002c0002t0078g0069 | 2 | HG00738.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.281-83065_281-8306 others(43): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(35): Show |
1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-83065_281-8306 others(46): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72048987
|
G | GAGAAGAA others(38): Show |
1 | a0001c0019t0054g0070 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-83065_281-8306 others(49): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72048987 | |||||
| chrX:72049003
|
A | AGAAGAG | 2 | a0001c0001t0037g0154a0002c0002t0007g0077 | 2 | HG04204.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.281-83071_281-8307 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049003 | |||||
| chrX:72049009
|
A | AGAAGAAG others(35): Show |
1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-83065_281-8306 others(46): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(38): Show |
2 | a0001c0001t0001g0138a0009c0010t0052g0185 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.281-83065_281-8306 others(49): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(23): Show |
3 | a0001c0001t0057g0103a0001c0003t0012g0058a0008c0017t0053g0059 | 3 | HG02717.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.281-83065_281-8306 others(34): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(29): Show |
1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-83065_281-8306 others(40): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(20): Show |
4 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0003t0033g0093others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-83065_281-8306 others(31): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(17): Show |
3 | a0001c0003t0012g0057a0001c0003t0084g0150a0002c0002t0002g0056 | 3 | HG02886.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.281-83065_281-8306 others(28): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(2): Show |
4 | a0001c0001t0001g0051a0001c0001t0003g0144a0001c0001t0023g0055others(1): Show | 4 | HG02630.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-83065_281-8306 others(13): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAAG others(8): Show |
1 | a0001c0001t0003g0050 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281-83065_281-8306 others(19): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAG | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(65): Show | 68 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.281-83040_281-8303 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAGG others(5): Show |
45 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(42): Show | 45 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.281-83046_281-8303 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | AGAAGAGG others(11): Show |
1 | a0002c0002t0076g0075 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.281-83052_281-8303 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049009
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0018g0132a0001c0001t0037g0154others(1): Show | 4 | HG02155.hp2 HG02698.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-83070A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049009 | ||||||
| chrX:72049009
|
AGAAGAG | A | 8 | a0001c0001t0051g0187a0002c0002t0002g0060a0002c0002t0002g0067others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-83040_281-8303 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049009 | |||||
| chrX:72049015
|
G | A | 29 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(26): Show | 29 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.281-83064G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049015 | ||||||
| chrX:72049021
|
G | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(19): Show | 22 | HG01109.hp1 HG01358.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-83058G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049021 | ||||||
| chrX:72049027
|
G | GGAAGAGG others(11): Show |
1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281-83041_281-8304 others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049027 | |||||
| chrX:72049029
|
A | AAGAGGAG | 1 | a0001c0001t0009g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.281-83044_281-8304 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049029 | |||||
| chrX:72049045
|
A | G | 5 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-83034A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049045 | ||||||
| chrX:72049057
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-83022G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049057 | ||||||
| chrX:72049061
|
C | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-83018C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049061 | ||||||
| chrX:72049064
|
G | C | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-83015G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049064 | ||||||
| chrX:72049077
|
A | AG | 1 | a0001c0001t0009g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.281-82998dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72049077 | |||||
| chrX:72049400
|
G | A | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-82679G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049400 | ||||||
| chrX:72049446
|
G | C | 1 | a0001c0003t0036g0054 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.281-82633G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049446 | ||||||
| chrX:72049468
|
C | T | 2 | a0001c0001t0001g0094a0002c0002t0002g0095 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.281-82611C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049468 | ||||||
| chrX:72049490
|
G | A | 1 | a0002c0002t0002g0171 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.281-82589G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049490 | ||||||
| chrX:72049502
|
C | G | 1 | a0001c0001t0042g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.281-82577C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049502 | ||||||
| chrX:72049730
|
A | C | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-82349A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049730 | ||||||
| chrX:72049977
|
G | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(28): Show | 31 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.281-82102G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72049977 | ||||||
| chrX:72050185
|
A | G | 8 | a0001c0001t0051g0187a0002c0002t0002g0060a0002c0002t0002g0067others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-81894A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72050185 | ||||||
| chrX:72050239
|
G | GT | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.281-81833dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72050239 | |||||
| chrX:72050275
|
G | A | 12 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0015g0049others(9): Show | 12 | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-81804G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72050275 | ||||||
| chrX:72050642
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.281-81437C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72050642 | ||||||
| chrX:72050890
|
C | CA | 1 | a0001c0001t0001g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.281-81176dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72050890 | |||||
| chrX:72050899
|
A | AC | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-81180_281-8117 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72050899 | ||||||
| chrX:72050953
|
G | A | 26 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(23): Show | 26 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.281-81126G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72050953 | ||||||
| chrX:72051115
|
T | A | 1 | a0003c0004t0008g0003 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.281-80964T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72051115 | ||||||
| chrX:72051207
|
A | G | 6 | a0002c0002t0002g0060a0002c0002t0002g0101a0002c0002t0002g0104others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-80872A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72051207 | ||||||
| chrX:72051826
|
C | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(28): Show | 31 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.281-80253C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72051826 | ||||||
| chrX:72051948
|
G | A | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-80131G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72051948 | ||||||
| chrX:72052024
|
A | G | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-80055A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052024 | ||||||
| chrX:72052212
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-79867G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052212 | ||||||
| chrX:72052238
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0009g0184others(1): Show | 4 | NA18965.hp1 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-79841G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052238 | ||||||
| chrX:72052278
|
G | A | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-79801G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052278 | ||||||
| chrX:72052309
|
C | G | 2 | a0001c0001t0004g0131a0001c0001t0024g0001 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.281-79770C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052309 | ||||||
| chrX:72052448
|
G | T | 2 | a0001c0001t0004g0131a0001c0001t0024g0001 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.281-79631G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052448 | ||||||
| chrX:72052768
|
A | G | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-79311A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052768 | ||||||
| chrX:72052773
|
G | A | 2 | a0001c0001t0004g0128a0002c0002t0007g0129 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.281-79306G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052773 | ||||||
| chrX:72052798
|
A | C | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-79281A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72052798 | ||||||
| chrX:72053071
|
A | G | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-79008A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72053071 | ||||||
| chrX:72053102
|
A | G | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-78977A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72053102 | ||||||
| chrX:72053456
|
C | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-78623C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72053456 | ||||||
| chrX:72054069
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281-78010C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72054069 | ||||||
| chrX:72054329
|
C | T | 1 | a0001c0001t0005g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281-77750C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72054329 | ||||||
| chrX:72054395
|
C | T | 3 | a0002c0002t0059g0029a0002c0002t0077g0183a0002c0002t0079g0165 | 3 | NA18940.hp1 NA18989.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.281-77684C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72054395 | ||||||
| chrX:72055048
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-77031C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055048 | ||||||
| chrX:72055094
|
T | G | 29 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(26): Show | 29 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.281-76985T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055094 | ||||||
| chrX:72055103
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-76976C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055103 | ||||||
| chrX:72055223
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-76856G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055223 | ||||||
| chrX:72055255
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.281-76824A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055255 | ||||||
| chrX:72055329
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281-76750C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055329 | ||||||
| chrX:72055675
|
G | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(68): Show | 71 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.281-76404G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055675 | ||||||
| chrX:72055783
|
C | G | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-76296C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055783 | ||||||
| chrX:72055812
|
G | A | 2 | a0001c0003t0028g0159a0001c0003t0084g0150 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.281-76267G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055812 | ||||||
| chrX:72055873
|
A | G | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-76206A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72055873 | ||||||
| chrX:72056012
|
G | GA | 4 | a0001c0001t0001g0030a0001c0001t0067g0148a0001c0003t0029g0149others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-76060dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72056012 | |||||
| chrX:72056253
|
C | T | 1 | a0002c0002t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.281-75826C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056253 | ||||||
| chrX:72056440
|
C | G | 1 | a0001c0001t0057g0103 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.281-75639C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056440 | ||||||
| chrX:72056470
|
C | G | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-75609C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056470 | ||||||
| chrX:72056552
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.281-75527G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056552 | ||||||
| chrX:72056552
|
G | GCA | 6 | a0001c0001t0001g0004a0001c0001t0001g0107a0001c0001t0022g0127others(3): Show | 6 | HG00438.hp1 HG00438.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-75501_281-7550 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72056552 | |||||
| chrX:72056552
|
G | GCACA | 12 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(9): Show | 12 | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-75503_281-7550 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72056552 | |||||
| chrX:72056552
|
G | GCACACA | 1 | a0001c0001t0001g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281-75505_281-7550 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72056552 | |||||
| chrX:72056552
|
GCA | G | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-75501_281-7550 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72056552 | |||||
| chrX:72056552
|
GCACACA | G | 1 | a0001c0001t0057g0103 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.281-75505_281-7550 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72056552 | |||||
| chrX:72056554
|
A | G | 29 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(26): Show | 29 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.281-75525A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056554 | ||||||
| chrX:72056580
|
G | A | 2 | a0001c0003t0070g0027a0010c0016t0075g0137 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-75499G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056580 | ||||||
| chrX:72056907
|
C | T | 1 | a0001c0001t0014g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.281-75172C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72056907 | ||||||
| chrX:72057648
|
A | G | 1 | a0001c0001t0010g0002 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.281-74431A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72057648 | ||||||
| chrX:72057727
|
C | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.281-74352C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72057727 | ||||||
| chrX:72058034
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0067g0148a0001c0003t0029g0149others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-74045T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72058034 | ||||||
| chrX:72058199
|
A | T | 2 | a0001c0001t0083g0113a0003c0004t0006g0112 | 2 | NA18967.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.281-73880A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72058199 | ||||||
| chrX:72058206
|
G | A | 1 | a0003c0004t0006g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.281-73873G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72058206 | ||||||
| chrX:72058333
|
CT | C | 2 | a0001c0001t0017g0166a0001c0001t0023g0055 | 2 | HG01069.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.281-73737delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72058333 | |||||
| chrX:72058345
|
A | G | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-73734A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72058345 | ||||||
| chrX:72058431
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.281-73648G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72058431 | ||||||
| chrX:72058506
|
A | G | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-73573A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72058506 | ||||||
| chrX:72059178
|
C | T | 28 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(25): Show | 28 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-72901C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72059178 | ||||||
| chrX:72059219
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281-72860C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72059219 | ||||||
| chrX:72059232
|
T | C | 1 | a0001c0014t0040g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.281-72847T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72059232 | ||||||
| chrX:72059835
|
C | T | 2 | a0001c0001t0046g0123a0007c0008t0001g0110 | 2 | HG01258.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.281-72244C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72059835 | ||||||
| chrX:72059886
|
A | G | 34 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(31): Show | 34 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.281-72193A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72059886 | ||||||
| chrX:72059946
|
A | G | 51 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(48): Show | 51 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(48): Show |
intron_variant | MODIFIER | c.281-72133A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72059946 | ||||||
| chrX:72060106
|
G | A | 30 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(27): Show | 30 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.281-71973G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72060106 | ||||||
| chrX:72060123
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.281-71956G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72060123 | ||||||
| chrX:72060268
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-71811C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72060268 | ||||||
| chrX:72060561
|
TG | T | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-71515delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72060561 | |||||
| chrX:72060943
|
A | C | 1 | a0001c0001t0023g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.281-71136A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72060943 | ||||||
| chrX:72061679
|
C | T | 28 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(25): Show | 28 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-70400C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72061679 | ||||||
| chrX:72061842
|
T | C | 34 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(31): Show | 34 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.281-70237T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72061842 | ||||||
| chrX:72062047
|
A | G | 8 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | HG02109.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-70032A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72062047 | ||||||
| chrX:72062237
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.281-69842C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72062237 | ||||||
| chrX:72062383
|
G | T | 3 | a0001c0001t0019g0160a0001c0001t0019g0161a0012c0018t0001g0147 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.281-69696G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72062383 | ||||||
| chrX:72062942
|
A | G | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(12): Show | 15 | HG02056.hp1 HG02129.hp1 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-69137A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72062942 | ||||||
| chrX:72062981
|
TG | T | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-69094delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72062981 | |||||
| chrX:72063023
|
TC | T | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-69053delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72063023 | |||||
| chrX:72063052
|
C | CG | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-69026dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72063052 | |||||
| chrX:72063052
|
C | T | 17 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0001t0005g0096others(14): Show | 17 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.281-69027C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063052 | ||||||
| chrX:72063423
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.281-68656G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063423 | ||||||
| chrX:72063639
|
G | A | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-68440G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063639 | ||||||
| chrX:72063676
|
C | T | 3 | a0001c0001t0019g0160a0001c0001t0019g0161a0012c0018t0001g0147 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.281-68403C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063676 | ||||||
| chrX:72063805
|
G | A | 8 | a0001c0001t0051g0187a0002c0002t0002g0060a0002c0002t0002g0067others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-68274G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063805 | ||||||
| chrX:72063863
|
C | T | 28 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0047others(25): Show | 28 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-68216C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063863 | ||||||
| chrX:72063922
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281-68157T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063922 | ||||||
| chrX:72063923
|
A | G | 4 | a0001c0001t0005g0146a0001c0001t0038g0158a0001c0001t0074g0142others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-68156A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72063923 | ||||||
| chrX:72064233
|
A | G | 2 | a0001c0001t0004g0128a0002c0002t0007g0129 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.281-67846A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72064233 | ||||||
| chrX:72065040
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.281-67039C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72065040 | ||||||
| chrX:72065091
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.281-66988G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72065091 | ||||||
| chrX:72065243
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.281-66836T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72065243 | ||||||
| chrX:72065304
|
A | T | 1 | a0001c0001t0005g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281-66775A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72065304 | ||||||
| chrX:72065430
|
A | C | 8 | a0001c0001t0051g0187a0002c0002t0002g0060a0002c0002t0002g0067others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-66649A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72065430 | ||||||
| chrX:72065709
|
A | C | 1 | a0003c0004t0004g0186 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.281-66370A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72065709 | ||||||
| chrX:72066112
|
C | G | 2 | a0001c0001t0057g0103a0008c0017t0053g0059 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.281-65967C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72066112 | ||||||
| chrX:72066250
|
T | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0033others(26): Show | 29 | HG00438.hp2 HG02015.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.281-65829T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72066250 | ||||||
| chrX:72066500
|
G | A | 3 | a0001c0001t0005g0146a0001c0001t0074g0142a0002c0002t0002g0143 | 3 | HG02258.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281-65579G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72066500 | ||||||
| chrX:72066505
|
A | C | 7 | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0003t0012g0057others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-65574A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72066505 | ||||||
| chrX:72066760
|
A | G | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-65319A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72066760 | ||||||
| chrX:72066896
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0010g0002a0001c0001t0081g0081 | 3 | HG02056.hp1 HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.281-65183G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72066896 | ||||||
| chrX:72067008
|
TG | T | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-65067delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72067008 | |||||
| chrX:72067097
|
C | T | 1 | a0007c0008t0001g0110 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.281-64982C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72067097 | ||||||
| chrX:72067146
|
A | AAAACAGA others(1): Show |
1 | a0001c0001t0009g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.281-64927_281-6492 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72067146 | |||||
| chrX:72067418
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0020others(92): Show | 95 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.281-64661A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72067418 | ||||||
| chrX:72067471
|
T | G | 1 | a0001c0001t0045g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.281-64608T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72067471 | ||||||
| chrX:72067822
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-64257C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72067822 | ||||||
| chrX:72067961
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.281-64118C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72067961 | ||||||
| chrX:72068051
|
T | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(135): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.281-64028T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068051 | ||||||
| chrX:72068103
|
A | G | 2 | a0001c0001t0068g0130a0003c0004t0004g0186 | 2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.281-63976A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068103 | ||||||
| chrX:72068173
|
A | G | 26 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0065others(23): Show | 26 | HG01243.hp1 HG02056.hp1 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.281-63906A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068173 | ||||||
| chrX:72068237
|
T | C | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-63842T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068237 | ||||||
| chrX:72068513
|
G | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0065others(29): Show | 32 | HG01243.hp1 HG02056.hp1 HG02129.hp1 others(29): Show |
intron_variant | MODIFIER | c.281-63566G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068513 | ||||||
| chrX:72068661
|
CGTGTGTG others(1): Show |
C | 2 | a0001c0001t0001g0138a0002c0002t0002g0086 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.281-63410_281-6340 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72068661 | |||||
| chrX:72068669
|
T | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0020others(94): Show | 97 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-63410T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068669 | ||||||
| chrX:72068675
|
TGAGAGAG others(3): Show |
T | 123 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(120): Show | 123 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.281-63388_281-6337 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72068675 | |||||
| chrX:72068677
|
A | T | 47 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0033others(44): Show | 47 | HG00438.hp2 HG00673.hp1 HG02027.hp1 others(44): Show |
intron_variant | MODIFIER | c.281-63402A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068677 | ||||||
| chrX:72068679
|
A | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0033others(28): Show | 31 | HG00438.hp2 HG00673.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.281-63400A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068679 | ||||||
| chrX:72068680
|
G | C | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-63399G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72068680 | ||||||
| chrX:72069195
|
C | T | 1 | a0005c0006t0058g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.281-62884C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72069195 | ||||||
| chrX:72069252
|
G | A | 24 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0065others(21): Show | 24 | HG01243.hp1 HG02056.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.281-62827G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72069252 | ||||||
| chrX:72069417
|
A | AAG | 1 | a0002c0002t0002g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281-62646_281-6264 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72069417 | |||||
| chrX:72069417
|
AAGAGAG | A | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-62650_281-6264 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72069417 | |||||
| chrX:72069421
|
G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0027g0025 | 3 | NA18965.hp1 NA18988.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.281-62658G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72069421 | ||||||
| chrX:72069631
|
AGAG | A | 3 | a0001c0001t0003g0050a0001c0001t0003g0144a0001c0001t0025g0015 | 3 | HG01243.hp1 HG03139.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.281-62434_281-6243 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72069631 | |||||
| chrX:72069659
|
G | A | 1 | a0001c0003t0028g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281-62420G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72069659 | ||||||
| chrX:72070314
|
C | T | 24 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0065others(21): Show | 24 | HG01243.hp1 HG02056.hp1 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.281-61765C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72070314 | ||||||
| chrX:72070787
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0065a0001c0001t0001g0115others(17): Show | 20 | HG01243.hp1 HG02056.hp1 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.281-61292C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72070787 | ||||||
| chrX:72070920
|
G | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | NA18970.hp1 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.281-61159G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72070920 | ||||||
| chrX:72071100
|
A | G | 2 | a0001c0001t0001g0138a0002c0002t0002g0086 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.281-60979A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72071100 | ||||||
| chrX:72071477
|
T | A | 76 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(73): Show | 76 | HG00438.hp2 HG00673.hp1 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.281-60602T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72071477 | ||||||
| chrX:72071544
|
G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0020others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.281-60535G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72071544 | ||||||
| chrX:72071749
|
A | G | 2 | a0001c0003t0028g0159a0001c0003t0084g0150 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.281-60330A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72071749 | ||||||
| chrX:72072874
|
TG | T | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.281-59202delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72072874 | |||||
| chrX:72073269
|
G | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(182): Show | 185 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.281-58810G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72073269 | ||||||
| chrX:72073446
|
G | T | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-58633G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72073446 | ||||||
| chrX:72073462
|
A | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(76): Show | 79 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.281-58617A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72073462 | ||||||
| chrX:72073469
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-58610C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72073469 | ||||||
| chrX:72073822
|
C | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0001g0074others(8): Show | 11 | HG01358.hp1 NA18612.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-58257C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72073822 | ||||||
| chrX:72074131
|
TC | T | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.281-57944delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72074131 | |||||
| chrX:72074154
|
AC | A | 19 | a0001c0001t0001g0017a0001c0001t0001g0065a0001c0001t0001g0115others(16): Show | 19 | HG01243.hp1 HG02056.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-57924delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72074154 | ||||||
| chrX:72074397
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0030others(28): Show | 31 | HG00438.hp2 HG00673.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.281-57682A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72074397 | ||||||
| chrX:72074555
|
G | A | 1 | a0001c0001t0017g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.281-57524G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72074555 | ||||||
| chrX:72074628
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.281-57451G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72074628 | ||||||
| chrX:72074695
|
T | C | 2 | a0001c0003t0028g0159a0001c0003t0084g0150 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.281-57384T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72074695 | ||||||
| chrX:72075536
|
A | G | 1 | a0001c0001t0055g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-56543A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72075536 | ||||||
| chrX:72075890
|
TG | T | 1 | a0001c0001t0009g0040 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.281-56184delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075890 | |||||
| chrX:72075901
|
A | AGT | 5 | a0001c0001t0022g0052a0001c0003t0036g0054a0002c0002t0002g0101others(2): Show | 5 | HG03098.hp1 HG03471.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-56151_281-5615 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075901 | |||||
| chrX:72075901
|
A | AGTGT | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(130): Show | 133 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.281-56153_281-5615 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075901 | |||||
| chrX:72075901
|
A | AGTGTGT | 3 | a0001c0001t0009g0040a0001c0001t0072g0038a0003c0004t0001g0043 | 3 | NA18960.hp1 NA19012.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.281-56155_281-5615 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075901 | |||||
| chrX:72075901
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0037a0001c0001t0001g0094a0001c0003t0084g0150 | 3 | HG02015.hp1 HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.281-56157_281-5615 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075901 | |||||
| chrX:72075901
|
AGT | A | 18 | a0001c0001t0001g0051a0001c0001t0001g0138a0001c0001t0005g0096others(15): Show | 18 | HG02258.hp1 HG02280.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-56151_281-5615 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075901 | |||||
| chrX:72075901
|
AGTGT | A | 21 | a0001c0001t0001g0017a0001c0001t0001g0065a0001c0001t0001g0115others(18): Show | 21 | HG01243.hp1 HG02056.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-56153_281-5615 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72075901 | |||||
| chrX:72076090
|
C | T | 1 | a0001c0001t0009g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.281-55989C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72076090 | ||||||
| chrX:72076175
|
T | C | 41 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0053others(38): Show | 41 | HG01243.hp1 HG02056.hp1 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.281-55904T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72076175 | ||||||
| chrX:72076184
|
T | C | 41 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0053others(38): Show | 41 | HG01243.hp1 HG02056.hp1 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.281-55895T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72076184 | ||||||
| chrX:72076352
|
T | C | 1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-55727T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72076352 | ||||||
| chrX:72076528
|
T | G | 8 | a0001c0001t0001g0053a0001c0001t0001g0138a0001c0003t0012g0057others(5): Show | 8 | HG02630.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-55551T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72076528 | ||||||
| chrX:72076588
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-55491G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72076588 | ||||||
| chrX:72076606
|
TG | T | 1 | a0001c0001t0001g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.281-55470delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72076606 | |||||
| chrX:72076922
|
TA | T | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.281-55155delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72076922 | |||||
| chrX:72076944
|
TG | T | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.281-55133delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72076944 | |||||
| chrX:72077197
|
A | C | 1 | a0001c0001t0001g0035 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.281-54882A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72077197 | ||||||
| chrX:72077328
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-54751C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72077328 | ||||||
| chrX:72077345
|
TG | T | 1 | a0001c0001t0009g0040 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.281-54729delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72077345 | |||||
| chrX:72078021
|
C | T | 3 | a0001c0001t0004g0066a0002c0002t0002g0118a0002c0002t0007g0077 | 3 | HG02735.hp1 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.281-54058C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72078021 | ||||||
| chrX:72078114
|
G | A | 2 | a0001c0001t0005g0091a0002c0002t0002g0141 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.281-53965G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72078114 | ||||||
| chrX:72078156
|
G | T | 5 | a0001c0001t0001g0051a0001c0001t0005g0146a0001c0001t0039g0151others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-53923G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72078156 | ||||||
| chrX:72078660
|
G | C | 1 | a0001c0001t0047g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281-53419G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72078660 | ||||||
| chrX:72078756
|
A | T | 1 | a0003c0004t0006g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.281-53323A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72078756 | ||||||
| chrX:72078863
|
A | G | 1 | a0001c0003t0011g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-53216A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72078863 | ||||||
| chrX:72079028
|
C | T | 4 | a0001c0001t0056g0092a0001c0001t0057g0103a0002c0002t0002g0086others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-53051C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72079028 | ||||||
| chrX:72079111
|
A | G | 1 | a0001c0001t0048g0168 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.281-52968A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72079111 | ||||||
| chrX:72079385
|
C | T | 4 | a0001c0001t0005g0096a0001c0001t0019g0160a0001c0001t0019g0161others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-52694C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72079385 | ||||||
| chrX:72079678
|
A | AG | 1 | a0001c0001t0001g0098 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.281-52399dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72079678 | |||||
| chrX:72079679
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.281-52400G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72079679 | ||||||
| chrX:72079814
|
G | GC | 1 | a0001c0001t0001g0098 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.281-52262dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72079814 | |||||
| chrX:72080017
|
GC | G | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-52059delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080017 | |||||
| chrX:72080151
|
C | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-51928C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72080151 | ||||||
| chrX:72080260
|
CG | C | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-51815delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080260 | |||||
| chrX:72080276
|
TG | T | 1 | a0001c0001t0005g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281-51798delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080276 | |||||
| chrX:72080416
|
G | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(67): Show | 70 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.281-51663G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72080416 | ||||||
| chrX:72080433
|
G | T | 1 | a0001c0001t0003g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.281-51646G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72080433 | ||||||
| chrX:72080449
|
G | A | 4 | a0001c0001t0056g0092a0001c0001t0057g0103a0002c0002t0002g0086others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-51630G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72080449 | ||||||
| chrX:72080571
|
C | CGT | 10 | a0001c0001t0001g0053a0001c0001t0018g0132a0001c0001t0056g0092others(7): Show | 10 | HG02523.hp2 HG02647.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-51477_281-5147 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGT | 47 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0034others(44): Show | 47 | HG00280.hp1 HG00609.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.281-51479_281-5147 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGTGT | 9 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(6): Show | 9 | HG02922.hp1 HG02922.hp2 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-51481_281-5147 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGTGTG others(1): Show |
20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(17): Show | 20 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.281-51483_281-5147 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGTGTG others(3): Show |
25 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0045others(22): Show | 25 | HG00621.hp1 HG01358.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-51485_281-5147 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGTGTG others(5): Show |
14 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0033others(11): Show | 14 | HG02015.hp1 HG02027.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-51487_281-5147 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGTGTG others(7): Show |
3 | a0001c0001t0009g0040a0001c0001t0055g0068a0003c0004t0008g0085 | 3 | HG00673.hp1 HG02451.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.281-51489_281-5147 others(18): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
C | CGTGTGTG others(9): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0072 | 2 | HG02040.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.281-51491_281-5147 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
CGT | C | 48 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0094others(45): Show | 48 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.281-51477_281-5147 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
CGTGT | C | 1 | a0001c0001t0018g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-51479_281-5147 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080571
|
CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0014g0125a0001c0013t0003g0122a0002c0002t0002g0124 | 3 | HG00140.hp1 HG01074.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.281-51483_281-5147 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72080571 | |||||
| chrX:72080725
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0005g0146a0001c0001t0039g0151others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-51354C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72080725 | ||||||
| chrX:72080847
|
C | G | 1 | a0002c0002t0007g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.281-51232C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72080847 | ||||||
| chrX:72081109
|
T | C | 1 | a0005c0006t0003g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.281-50970T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72081109 | ||||||
| chrX:72081449
|
CT | C | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-50627delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72081449 | |||||
| chrX:72081479
|
AG | A | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-50598delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72081479 | |||||
| chrX:72081571
|
C | T | 1 | a0001c0001t0004g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.281-50508C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72081571 | ||||||
| chrX:72081673
|
A | T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.281-50406A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72081673 | ||||||
| chrX:72081778
|
T | TA | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-50299dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72081778 | |||||
| chrX:72081977
|
TC | T | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-50100delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72081977 | |||||
| chrX:72082238
|
T | TA | 1 | a0001c0001t0065g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281-49840dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72082238 | |||||
| chrX:72082635
|
C | T | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-49444C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72082635 | ||||||
| chrX:72082832
|
AG | A | 1 | a0001c0001t0001g0098 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.281-49246delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72082832 | ||||||
| chrX:72082852
|
GC | G | 1 | a0001c0001t0009g0040 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.281-49223delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72082852 | |||||
| chrX:72082896
|
G | A | 2 | a0001c0001t0001g0030a0006c0007t0013g0090 | 2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.281-49183G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72082896 | ||||||
| chrX:72083149
|
T | TC | 1 | a0001c0001t0001g0098 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.281-48924dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72083149 | |||||
| chrX:72083522
|
G | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(72): Show | 75 | HG00438.hp2 HG00673.hp1 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.281-48557G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72083522 | ||||||
| chrX:72083692
|
G | C | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-48387G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72083692 | ||||||
| chrX:72083941
|
C | T | 3 | a0001c0001t0005g0096a0001c0001t0019g0160a0001c0001t0019g0161 | 3 | HG01167.hp1 HG01169.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.281-48138C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72083941 | ||||||
| chrX:72084143
|
C | G | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-47936C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72084143 | ||||||
| chrX:72084207
|
A | AG | 1 | a0001c0001t0027g0025 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.281-47867dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72084207 | |||||
| chrX:72084398
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.281-47681T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72084398 | ||||||
| chrX:72084441
|
A | G | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-47638A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72084441 | ||||||
| chrX:72084883
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-47196C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72084883 | ||||||
| chrX:72085259
|
C | T | 3 | a0001c0001t0001g0138a0002c0002t0002g0086a0008c0017t0053g0059 | 3 | HG02717.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.281-46820C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085259 | ||||||
| chrX:72085464
|
C | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0017others(104): Show | 107 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.281-46615C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085464 | ||||||
| chrX:72085624
|
T | C | 8 | a0002c0002t0002g0060a0002c0002t0002g0101a0002c0002t0002g0104others(5): Show | 8 | HG00738.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-46455T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085624 | ||||||
| chrX:72085704
|
G | GT | 19 | a0001c0001t0001g0047a0001c0001t0001g0115a0001c0001t0001g0138others(16): Show | 19 | HG01243.hp1 HG02056.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-46365dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085704 | |||||
| chrX:72085712
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.281-46367T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085712 | ||||||
| chrX:72085714
|
T | TTG | 1 | a0001c0001t0047g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281-46365_281-4636 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085714 | ||||||
| chrX:72085715
|
G | GT | 35 | a0001c0001t0001g0126a0001c0001t0001g0177a0001c0001t0003g0097others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.281-46352dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085715 | |||||
| chrX:72085715
|
G | GTT | 1 | a0001c0001t0014g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.281-46353_281-4635 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085715 | |||||
| chrX:72085715
|
G | T | 4 | a0001c0001t0047g0117a0001c0001t0072g0038a0003c0004t0008g0003others(1): Show | 4 | HG02630.hp1 HG03834.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-46364G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085715 | ||||||
| chrX:72085715
|
GT | G | 8 | a0002c0002t0002g0060a0002c0002t0002g0101a0002c0002t0002g0104others(5): Show | 8 | HG00738.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-46352delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085715 | |||||
| chrX:72085715
|
GTTT | G | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-46354_281-4635 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085715 | |||||
| chrX:72085716
|
T | G | 3 | a0001c0001t0072g0038a0003c0004t0008g0003a0009c0010t0052g0185 | 3 | HG02630.hp1 NA19068.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.281-46363T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085716 | ||||||
| chrX:72085736
|
G | C | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-46343G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085736 | ||||||
| chrX:72085741
|
GT | G | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-46335delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085741 | |||||
| chrX:72085754
|
ACCACATA others(85): Show |
A | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-46322_281-4623 others(96): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085754 | |||||
| chrX:72085801
|
G | A | 1 | a0001c0001t0014g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.281-46278G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72085801 | ||||||
| chrX:72085819
|
ACTCCCTC others(24): Show |
A | 1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281-46254_281-4622 others(35): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72085819 | |||||
| chrX:72086020
|
T | A | 3 | a0001c0003t0011g0155a0001c0003t0011g0156a0002c0002t0002g0157 | 3 | HG02976.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.281-46059T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72086020 | ||||||
| chrX:72086059
|
C | A | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-46020C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72086059 | ||||||
| chrX:72086320
|
TC | T | 10 | a0001c0001t0001g0053a0001c0001t0022g0052a0001c0001t0055g0068others(7): Show | 10 | HG02451.hp2 HG02559.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-45757delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72086320 | |||||
| chrX:72086454
|
C | A | 1 | a0001c0001t0068g0130 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.281-45625C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72086454 | ||||||
| chrX:72086455
|
G | A | 1 | a0002c0002t0078g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281-45624G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72086455 | ||||||
| chrX:72086683
|
C | CA | 10 | a0001c0001t0003g0050a0001c0001t0003g0144a0001c0001t0004g0116others(7): Show | 10 | HG00621.hp1 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-45371dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72086683 | |||||
| chrX:72086683
|
C | CAA | 1 | a0001c0001t0017g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.281-45372_281-4537 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72086683 | |||||
| chrX:72086683
|
CA | C | 12 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | HG00738.hp1 HG02109.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-45371delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72086683 | |||||
| chrX:72086683
|
CAA | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0037others(28): Show | 31 | HG01433.hp1 HG02015.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.281-45372_281-4537 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72086683 | |||||
| chrX:72086683
|
CAAA | C | 53 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(50): Show | 53 | HG00438.hp2 HG00673.hp1 HG02071.hp1 others(50): Show |
intron_variant | MODIFIER | c.281-45373_281-4537 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72086683 | |||||
| chrX:72086790
|
A | G | 13 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.281-45289A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72086790 | ||||||
| chrX:72087435
|
G | A | 6 | a0001c0001t0005g0091a0001c0001t0067g0148a0001c0003t0028g0159others(3): Show | 6 | HG01109.hp1 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-44644G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72087435 | ||||||
| chrX:72087765
|
G | A | 1 | a0001c0003t0029g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.281-44314G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72087765 | ||||||
| chrX:72087768
|
A | C | 3 | a0001c0001t0017g0166a0001c0001t0037g0154a0001c0001t0051g0187 | 3 | HG01069.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.281-44311A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72087768 | ||||||
| chrX:72087829
|
G | A | 1 | a0001c0003t0035g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.281-44250G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72087829 | ||||||
| chrX:72087961
|
TTGGGAGG others(19): Show |
T | 31 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(28): Show | 31 | HG00438.hp2 HG01433.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.281-44094_281-4406 others(30): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72087961 | |||||
| chrX:72088163
|
A | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-43916A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72088163 | ||||||
| chrX:72088212
|
C | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(95): Show | 98 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.281-43867C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72088212 | ||||||
| chrX:72088231
|
C | CA | 3 | a0001c0001t0001g0035a0001c0001t0019g0160a0001c0001t0019g0161 | 3 | HG01167.hp1 HG01169.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.281-43840dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72088231 | |||||
| chrX:72088307
|
G | A | 1 | a0003c0004t0008g0003 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.281-43772G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72088307 | ||||||
| chrX:72088797
|
A | G | 1 | a0001c0001t0046g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.281-43282A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72088797 | ||||||
| chrX:72088938
|
G | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(98): Show | 101 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.281-43141G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72088938 | ||||||
| chrX:72089071
|
G | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(96): Show | 99 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.281-43008G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72089071 | ||||||
| chrX:72089249
|
T | TA | 23 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(20): Show | 23 | HG00438.hp1 HG00621.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.281-42816dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72089249 | |||||
| chrX:72089249
|
TA | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(90): Show | 93 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.281-42816delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72089249 | |||||
| chrX:72089249
|
TAA | T | 7 | a0001c0001t0056g0092a0001c0003t0011g0155a0001c0003t0011g0156others(4): Show | 7 | HG02818.hp1 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-42817_281-4281 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72089249 | |||||
| chrX:72089675
|
C | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(98): Show | 101 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.281-42404C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72089675 | ||||||
| chrX:72089857
|
CA | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(33): Show | 36 | HG00438.hp2 HG00738.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.281-42212delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72089857 | |||||
| chrX:72089896
|
T | TA | 1 | a0001c0001t0047g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281-42177dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72089896 | |||||
| chrX:72090071
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-42008G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72090071 | ||||||
| chrX:72090154
|
C | T | 1 | a0001c0001t0073g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-41925C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72090154 | ||||||
| chrX:72090303
|
G | A | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-41776G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72090303 | ||||||
| chrX:72090580
|
C | T | 1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281-41499C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72090580 | ||||||
| chrX:72090772
|
A | AGT | 11 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 11 | HG00673.hp1 HG01258.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-41272_281-4127 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090772 | |||||
| chrX:72090772
|
A | AGTGT | 4 | a0001c0001t0037g0154a0001c0001t0083g0113a0001c0003t0028g0159others(1): Show | 4 | HG02615.hp2 HG03225.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-41274_281-4127 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090772 | |||||
| chrX:72090772
|
AGT | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0051others(25): Show | 28 | HG00280.hp1 HG00438.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-41272_281-4127 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090772 | |||||
| chrX:72090772
|
AGTGT | A | 12 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0094others(9): Show | 12 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.281-41274_281-4127 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090772 | |||||
| chrX:72090772
|
AGTGTGT | A | 8 | a0001c0001t0055g0068a0001c0003t0011g0155a0001c0003t0011g0156others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-41276_281-4127 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090772 | |||||
| chrX:72090772
|
AGTGTGTG others(3): Show |
A | 1 | a0002c0002t0002g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281-41280_281-4127 others(14): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090772 | |||||
| chrX:72090816
|
G | T | 1 | a0001c0001t0062g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.281-41263G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72090816 | ||||||
| chrX:72090830
|
AAGAT | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0053others(8): Show | 11 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.281-41245_281-4124 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72090830 | |||||
| chrX:72090886
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-41193C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72090886 | ||||||
| chrX:72091158
|
A | C | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-40921A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091158 | ||||||
| chrX:72091338
|
C | T | 64 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(61): Show | 64 | HG00673.hp1 HG02071.hp1 HG02132.hp1 others(61): Show |
intron_variant | MODIFIER | c.281-40741C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091338 | ||||||
| chrX:72091405
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-40674G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091405 | ||||||
| chrX:72091441
|
G | A | 1 | a0002c0002t0002g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.281-40638G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091441 | ||||||
| chrX:72091453
|
C | CA | 56 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 56 | HG00673.hp1 HG02071.hp1 HG02132.hp1 others(53): Show |
intron_variant | MODIFIER | c.281-40612dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72091453 | |||||
| chrX:72091453
|
CA | C | 1 | a0001c0001t0055g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-40612delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72091453 | |||||
| chrX:72091453
|
CAA | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(18): Show | 21 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-40613_281-4061 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72091453 | |||||
| chrX:72091506
|
G | A | 1 | a0001c0001t0025g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.281-40573G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091506 | ||||||
| chrX:72091543
|
G | A | 1 | a0001c0001t0015g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281-40536G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091543 | ||||||
| chrX:72091797
|
C | G | 3 | a0002c0002t0002g0060a0002c0002t0002g0101a0002c0002t0013g0102 | 3 | HG02886.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.281-40282C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091797 | ||||||
| chrX:72091896
|
T | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(19): Show | 22 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-40183T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72091896 | ||||||
| chrX:72091989
|
A | AAC | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-40075_281-4007 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72091989 | |||||
| chrX:72092185
|
A | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(19): Show | 22 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-39894A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72092185 | ||||||
| chrX:72092264
|
T | C | 1 | a0005c0006t0003g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.281-39815T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72092264 | ||||||
| chrX:72092383
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(12): Show | 15 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-39696C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72092383 | ||||||
| chrX:72092415
|
A | G | 1 | a0003c0004t0008g0003 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.281-39664A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72092415 | ||||||
| chrX:72092576
|
C | T | 1 | a0003c0004t0006g0083 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.281-39503C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72092576 | ||||||
| chrX:72092749
|
C | A | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-39330C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72092749 | ||||||
| chrX:72092752
|
T | TAACTGCA others(530): Show |
1 | a0001c0003t0084g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-39309_281-3930 others(541): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72092752 | |||||
| chrX:72092752
|
T | TAACTGCA others(531): Show |
2 | a0001c0001t0067g0148a0009c0010t0052g0185 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.281-39309_281-3930 others(542): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72092752 | |||||
| chrX:72092752
|
T | TAACTGCA others(516): Show |
1 | a0001c0003t0030g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.281-39309_281-3930 others(527): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72092752 | |||||
| chrX:72092752
|
T | TAACTGCA others(516): Show |
1 | a0001c0003t0034g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.281-39309_281-3930 others(527): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72092752 | |||||
| chrX:72093001
|
A | G | 8 | a0001c0001t0055g0068a0001c0003t0011g0155a0001c0003t0011g0156others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-39078A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093001 | ||||||
| chrX:72093328
|
G | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.281-38751G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093328 | ||||||
| chrX:72093398
|
G | T | 5 | a0001c0001t0067g0148a0001c0003t0030g0152a0001c0003t0034g0153others(2): Show | 5 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-38681G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093398 | ||||||
| chrX:72093400
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-38679C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093400 | ||||||
| chrX:72093646
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-38433G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093646 | ||||||
| chrX:72093712
|
A | AGCTT | 22 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0114others(19): Show | 22 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-38358_281-3835 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
A | AGCTTGCT others(1): Show |
2 | a0001c0001t0067g0148a0002c0002t0002g0118 | 2 | HG02109.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.281-38362_281-3835 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
A | AGCTTGCT others(5): Show |
1 | a0001c0001t0045g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.281-38366_281-3835 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
A | AGCTTGCT others(9): Show |
4 | a0001c0001t0001g0004a0001c0001t0056g0092a0001c0014t0040g0167others(1): Show | 4 | HG00438.hp1 HG01358.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-38355_281-3835 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
A | AGCTTGCT others(13): Show |
3 | a0001c0001t0004g0066a0001c0015t0032g0031a0002c0002t0002g0095 | 3 | HG02486.hp1 HG02615.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.281-38355_281-3835 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
A | AGCTTGCT others(17): Show |
2 | a0001c0001t0001g0115a0001c0001t0004g0014 | 2 | HG02056.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.281-38355_281-3835 others(28): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
AGCTT | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0053a0001c0001t0001g0099others(2): Show | 5 | HG02647.hp1 HG02698.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-38358_281-3835 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093712
|
AGCTTGCT others(1): Show |
A | 2 | a0001c0001t0001g0108a0001c0001t0062g0036 | 2 | HG04199.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.281-38362_281-3835 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093712 | |||||
| chrX:72093713
|
G | GCTTT | 10 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0100others(7): Show | 10 | HG01069.hp1 HG02071.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.281-38363_281-3836 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093713
|
G | GCTTTCTT others(1): Show |
3 | a0001c0001t0010g0084a0001c0003t0030g0152a0004c0005t0001g0088 | 3 | HG02976.hp2 NA18995.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.281-38363_281-3836 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093713
|
G | GCTTTCTT others(5): Show |
9 | a0001c0001t0015g0135a0001c0001t0021g0006a0001c0001t0022g0127others(6): Show | 9 | HG02615.hp2 HG03225.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-38363_281-3836 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093713
|
G | GCTTTCTT others(9): Show |
4 | a0001c0001t0021g0007a0003c0004t0004g0186a0003c0004t0008g0071others(1): Show | 4 | HG00673.hp1 NA19009.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-38363_281-3836 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093713
|
G | GCTTTCTT others(13): Show |
2 | a0001c0003t0070g0027a0003c0004t0061g0136 | 2 | HG06807.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.281-38363_281-3836 others(24): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093713
|
G | GCTTTCTT others(21): Show |
1 | a0004c0005t0001g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.281-38363_281-3836 others(32): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093713
|
GCTTGCTT others(5): Show |
G | 2 | a0001c0001t0001g0162a0001c0001t0074g0142 | 2 | HG02523.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.281-38362_281-3835 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093713 | |||||
| chrX:72093717
|
G | GCTTT | 6 | a0001c0001t0083g0113a0001c0003t0036g0054a0002c0002t0002g0101others(3): Show | 6 | HG02572.hp1 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-38359_281-3835 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093717 | |||||
| chrX:72093717
|
G | GCTTTCTT others(1): Show |
2 | a0001c0001t0064g0009a0002c0002t0002g0141 | 2 | HG03098.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.281-38359_281-3835 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093717 | |||||
| chrX:72093717
|
G | GCTTTCTT others(5): Show |
1 | a0001c0001t0009g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.281-38359_281-3835 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093717 | |||||
| chrX:72093717
|
G | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0023others(39): Show | 42 | HG00673.hp1 HG01069.hp1 HG02071.hp1 others(39): Show |
intron_variant | MODIFIER | c.281-38362G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093717 | ||||||
| chrX:72093717
|
GCTTGCTT others(1): Show |
G | 2 | a0001c0003t0011g0155a0001c0003t0084g0150 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.281-38358_281-3835 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093717 | |||||
| chrX:72093717
|
GCTTGCTT others(5): Show |
G | 2 | a0001c0001t0025g0015a0002c0002t0002g0060 | 2 | HG03490.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.281-38358_281-3834 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093717 | |||||
| chrX:72093717
|
GCTTGCTT others(9): Show |
G | 1 | a0001c0003t0011g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.281-38358_281-3834 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093717 | |||||
| chrX:72093721
|
G | GCTTGCTT others(21): Show |
1 | a0001c0003t0031g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.281-38355_281-3835 others(32): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
G | GCTTGCTT others(17): Show |
1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-38355_281-3835 others(28): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
G | GCTTGCTT others(1): Show |
1 | a0001c0001t0060g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.281-38355_281-3835 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
G | GCTTT | 15 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0024others(12): Show | 15 | HG01169.hp1 HG02717.hp1 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-38301_281-3829 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
G | GCTTTCTT others(1): Show |
5 | a0001c0001t0019g0161a0001c0001t0027g0025a0002c0002t0002g0056others(2): Show | 5 | HG01167.hp1 HG02970.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-38305_281-3829 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
G | GCTTTCTT others(9): Show |
1 | a0001c0001t0004g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.281-38313_281-3829 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
G | T | 63 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(60): Show | 63 | HG00673.hp1 HG01069.hp1 HG02071.hp1 others(60): Show |
intron_variant | MODIFIER | c.281-38358G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093721 | ||||||
| chrX:72093721
|
GCTTT | G | 17 | a0001c0001t0001g0178a0001c0001t0004g0128a0001c0001t0014g0173others(14): Show | 17 | HG01261.hp1 HG01934.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.281-38301_281-3829 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093721
|
GCTTTCTT others(1): Show |
G | 2 | a0001c0001t0017g0120a0001c0001t0037g0154 | 2 | HG00280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.281-38305_281-3829 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093721 | |||||
| chrX:72093725
|
T | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0003g0050others(27): Show | 30 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.281-38354T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093725 | ||||||
| chrX:72093729
|
T | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0089a0001c0001t0001g0178others(18): Show | 21 | HG00438.hp1 HG00609.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-38350T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093729 | ||||||
| chrX:72093733
|
T | G | 7 | a0001c0001t0005g0096a0001c0001t0017g0120a0001c0001t0037g0154others(4): Show | 7 | HG00280.hp1 HG01358.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-38346T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093733 | ||||||
| chrX:72093737
|
T | G | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-38342T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093737 | ||||||
| chrX:72093741
|
T | G | 1 | a0001c0001t0005g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-38338T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093741 | ||||||
| chrX:72093774
|
CTTTCTTT | C | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-38303_281-3829 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093774 | |||||
| chrX:72093778
|
C | CT | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.281-38297dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093778 | |||||
| chrX:72093779
|
T | TTTCTTTC | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-38298_281-3829 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093779 | |||||
| chrX:72093779
|
T | TTTCTTTC others(12): Show |
1 | a0001c0019t0054g0070 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-38298_281-3829 others(23): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093779 | |||||
| chrX:72093779
|
T | TTTCTTTC others(16): Show |
1 | a0003c0004t0063g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.281-38298_281-3829 others(27): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72093779 | |||||
| chrX:72093826
|
G | A | 5 | a0001c0001t0067g0148a0001c0003t0030g0152a0001c0003t0034g0153others(2): Show | 5 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-38253G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72093826 | ||||||
| chrX:72094140
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.281-37939T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72094140 | ||||||
| chrX:72094284
|
A | G | 3 | a0001c0001t0001g0051a0001c0001t0005g0146a0001c0001t0039g0151 | 3 | HG02258.hp1 HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.281-37795A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72094284 | ||||||
| chrX:72094353
|
AGTTTATT | A | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-37719_281-3771 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72094353 | |||||
| chrX:72094516
|
T | TA | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-37552dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72094516 | |||||
| chrX:72094870
|
A | AT | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-37206dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72094870 | |||||
| chrX:72095033
|
C | G | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-37046C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72095033 | ||||||
| chrX:72095148
|
C | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(13): Show | 16 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-36931C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72095148 | ||||||
| chrX:72095310
|
G | T | 2 | a0001c0003t0030g0152a0001c0003t0034g0153 | 2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.281-36769G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72095310 | ||||||
| chrX:72095324
|
ATCT | A | 1 | a0002c0002t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.281-36750_281-3674 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72095324 | |||||
| chrX:72095634
|
C | A | 1 | a0008c0017t0053g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281-36445C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72095634 | ||||||
| chrX:72095695
|
G | A | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-36384G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72095695 | ||||||
| chrX:72095867
|
A | G | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-36212A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72095867 | ||||||
| chrX:72095873
|
G | GT | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-36201dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72095873 | |||||
| chrX:72096289
|
C | T | 4 | a0001c0001t0001g0138a0002c0002t0002g0086a0002c0002t0078g0069others(1): Show | 4 | HG00738.hp1 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-35790C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096289 | ||||||
| chrX:72096560
|
G | A | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-35519G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096560 | ||||||
| chrX:72096606
|
T | G | 2 | a0001c0003t0031g0140a0002c0002t0002g0095 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.281-35473T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096606 | ||||||
| chrX:72096643
|
A | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(111): Show | 114 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.281-35436A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096643 | ||||||
| chrX:72096789
|
T | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-35290T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096789 | ||||||
| chrX:72096858
|
C | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-35221C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096858 | ||||||
| chrX:72096930
|
G | A | 1 | a0002c0002t0076g0075 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.281-35149G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72096930 | ||||||
| chrX:72097219
|
G | A | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-34860G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72097219 | ||||||
| chrX:72097399
|
G | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(19): Show | 22 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-34680G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72097399 | ||||||
| chrX:72097454
|
T | C | 1 | a0003c0004t0001g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.281-34625T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72097454 | ||||||
| chrX:72097455
|
C | G | 2 | a0001c0001t0017g0166a0001c0001t0051g0187 | 2 | HG01069.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.281-34624C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72097455 | ||||||
| chrX:72097550
|
T | A | 1 | a0002c0002t0002g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.281-34529T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72097550 | ||||||
| chrX:72097554
|
G | T | 1 | a0002c0002t0002g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.281-34525G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72097554 | ||||||
| chrX:72098140
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(9): Show | 12 | HG00438.hp1 HG01358.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-33939T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098140 | ||||||
| chrX:72098249
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(9): Show | 12 | HG00438.hp1 HG01358.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-33830A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098249 | ||||||
| chrX:72098264
|
T | C | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-33815T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098264 | ||||||
| chrX:72098390
|
C | T | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-33689C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098390 | ||||||
| chrX:72098445
|
G | GC | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-33634_281-3363 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098445 | ||||||
| chrX:72098577
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(11): Show | 14 | HG00438.hp1 HG01069.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-33502T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098577 | ||||||
| chrX:72098580
|
C | CA | 32 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0047others(29): Show | 32 | HG00438.hp2 HG00673.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.281-33483dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72098580 | |||||
| chrX:72098580
|
C | CAA | 3 | a0001c0001t0001g0045a0001c0001t0001g0074a0002c0002t0077g0183 | 3 | HG02074.hp1 NA18989.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.281-33484_281-3348 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72098580 | |||||
| chrX:72098580
|
CA | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(19): Show | 22 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-33483delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72098580 | |||||
| chrX:72098599
|
A | G | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-33480A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098599 | ||||||
| chrX:72098607
|
A | G | 1 | a0002c0002t0078g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281-33472A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098607 | ||||||
| chrX:72098727
|
C | T | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.281-33352C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72098727 | ||||||
| chrX:72099226
|
A | C | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.281-32853A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72099226 | ||||||
| chrX:72099357
|
A | G | 68 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(65): Show | 68 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(65): Show |
intron_variant | MODIFIER | c.281-32722A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72099357 | ||||||
| chrX:72099361
|
A | AT | 48 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 48 | HG00438.hp2 HG00621.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.281-32696dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72099361 | |||||
| chrX:72099361
|
A | ATT | 16 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(13): Show | 16 | HG00438.hp1 HG01358.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-32697_281-3269 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72099361 | |||||
| chrX:72099361
|
AT | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00673.hp1 HG02071.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.281-32696delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72099361 | |||||
| chrX:72099427
|
G | A | 1 | a0001c0001t0041g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.281-32652G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72099427 | ||||||
| chrX:72099437
|
C | T | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.281-32642C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72099437 | ||||||
| chrX:72099509
|
G | GC | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-32565dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72099509 | |||||
| chrX:72099555
|
G | A | 1 | a0001c0001t0025g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.281-32524G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72099555 | ||||||
| chrX:72099711
|
GA | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(9): Show | 12 | HG00438.hp1 HG01358.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-32363delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72099711 | |||||
| chrX:72100018
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | NA18970.hp1 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.281-32061T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100018 | ||||||
| chrX:72100022
|
A | G | 1 | a0001c0001t0025g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.281-32057A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100022 | ||||||
| chrX:72100117
|
C | T | 8 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0001t0067g0148others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-31962C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100117 | ||||||
| chrX:72100359
|
C | G | 2 | a0001c0003t0030g0152a0001c0003t0034g0153 | 2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.281-31720C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100359 | ||||||
| chrX:72100370
|
C | T | 1 | a0001c0003t0070g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281-31709C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100370 | ||||||
| chrX:72100624
|
G | A | 68 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(65): Show | 68 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(65): Show |
intron_variant | MODIFIER | c.281-31455G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100624 | ||||||
| chrX:72100697
|
T | G | 10 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0053others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.281-31382T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100697 | ||||||
| chrX:72100754
|
A | G | 8 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0001t0067g0148others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-31325A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100754 | ||||||
| chrX:72100936
|
C | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0066others(19): Show | 22 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.281-31143C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72100936 | ||||||
| chrX:72101038
|
C | CT | 5 | a0001c0001t0005g0091a0001c0020t0005g0012a0002c0002t0077g0183others(2): Show | 5 | HG01109.hp1 HG02257.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-31025dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72101038 | |||||
| chrX:72101038
|
CT | C | 4 | a0001c0001t0003g0181a0001c0001t0026g0172a0001c0001t0046g0123others(1): Show | 4 | HG01106.hp1 HG01192.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-31025delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72101038 | |||||
| chrX:72101186
|
TG | T | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-30892delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101186 | ||||||
| chrX:72101192
|
C | T | 1 | a0001c0001t0018g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-30887C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101192 | ||||||
| chrX:72101277
|
C | T | 1 | a0001c0011t0003g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.281-30802C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101277 | ||||||
| chrX:72101576
|
C | CT | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-30503_281-3050 others(5): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101576 | ||||||
| chrX:72101619
|
G | A | 1 | a0001c0001t0062g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.281-30460G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101619 | ||||||
| chrX:72101639
|
C | T | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-30440C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101639 | ||||||
| chrX:72101762
|
ACTG | A | 1 | a0002c0002t0002g0171 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.281-30312_281-3031 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72101762 | |||||
| chrX:72101802
|
T | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(11): Show | 14 | HG00438.hp1 HG01069.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-30277T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72101802 | ||||||
| chrX:72102243
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0066others(8): Show | 11 | HG00438.hp1 HG01358.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-29836C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102243 | ||||||
| chrX:72102375
|
C | T | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.281-29704C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102375 | ||||||
| chrX:72102522
|
T | C | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.281-29557T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102522 | ||||||
| chrX:72102552
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0027g0025 | 3 | NA18965.hp1 NA18988.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.281-29527G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102552 | ||||||
| chrX:72102729
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.281-29350G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102729 | ||||||
| chrX:72102752
|
G | GAGTC | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-29327_281-2932 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102752 | ||||||
| chrX:72102753
|
G | A | 1 | a0002c0002t0077g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-29326G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102753 | ||||||
| chrX:72102898
|
C | T | 1 | a0002c0002t0007g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.281-29181C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102898 | ||||||
| chrX:72102932
|
G | A | 1 | a0001c0001t0038g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281-29147G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72102932 | ||||||
| chrX:72103250
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(114): Show | 117 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(114): Show |
intron_variant | MODIFIER | c.281-28829G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72103250 | ||||||
| chrX:72103395
|
A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(21): Show | 24 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.281-28684A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72103395 | ||||||
| chrX:72103539
|
T | A | 1 | a0001c0001t0055g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-28540T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72103539 | ||||||
| chrX:72103578
|
G | C | 1 | a0001c0003t0012g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-28501G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72103578 | ||||||
| chrX:72103681
|
C | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(23): Show | 26 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.281-28398C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72103681 | ||||||
| chrX:72104139
|
G | T | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-27940G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72104139 | ||||||
| chrX:72104277
|
C | T | 3 | a0001c0003t0012g0057a0001c0003t0012g0058a0001c0003t0033g0093 | 3 | HG02809.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.281-27802C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72104277 | ||||||
| chrX:72104497
|
A | G | 1 | a0001c0001t0018g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-27582A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72104497 | ||||||
| chrX:72104586
|
T | C | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-27493T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72104586 | ||||||
| chrX:72104698
|
T | C | 1 | a0001c0001t0062g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.281-27381T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72104698 | ||||||
| chrX:72104960
|
TG | T | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-27116delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72104960 | |||||
| chrX:72105300
|
G | C | 8 | a0001c0001t0055g0068a0001c0003t0011g0155a0001c0003t0011g0156others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-26779G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105300 | ||||||
| chrX:72105522
|
G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0045others(17): Show | 20 | HG00438.hp2 HG01433.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.281-26557G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105522 | ||||||
| chrX:72105536
|
A | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(11): Show | 14 | HG00438.hp1 HG01069.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-26543A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105536 | ||||||
| chrX:72105650
|
G | T | 8 | a0001c0001t0055g0068a0001c0003t0011g0155a0001c0003t0011g0156others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-26429G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105650 | ||||||
| chrX:72105683
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(21): Show | 24 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.281-26396G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105683 | ||||||
| chrX:72105759
|
GA | G | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-26318delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72105759 | |||||
| chrX:72105769
|
CT | C | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-26308delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72105769 | |||||
| chrX:72105808
|
G | A | 6 | a0001c0001t0067g0148a0001c0003t0030g0152a0001c0003t0034g0153others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-26271G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105808 | ||||||
| chrX:72105935
|
C | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-26144C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105935 | ||||||
| chrX:72105937
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-26142C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105937 | ||||||
| chrX:72105947
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0162 | 2 | HG02523.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.281-26132C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105947 | ||||||
| chrX:72105975
|
T | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(118): Show | 121 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(118): Show |
intron_variant | MODIFIER | c.281-26104T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105975 | ||||||
| chrX:72105981
|
G | C | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-26098G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72105981 | ||||||
| chrX:72106134
|
CG | C | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25938delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106134 | |||||
| chrX:72106135
|
G | C | 1 | a0001c0001t0018g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-25944G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72106135 | ||||||
| chrX:72106137
|
G | C | 1 | a0001c0001t0014g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.281-25942G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72106137 | ||||||
| chrX:72106207
|
TA | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0108a0003c0004t0006g0082 | 3 | NA18953.hp1 NA18962.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.281-25860delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106207 | |||||
| chrX:72106251
|
T | TAC | 6 | a0001c0001t0017g0166a0001c0001t0037g0154a0001c0001t0051g0187others(3): Show | 6 | HG01069.hp1 HG02486.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-25806_281-2580 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106251 | |||||
| chrX:72106251
|
TAC | T | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-25806_281-2580 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106251 | |||||
| chrX:72106263
|
C | CA | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25815dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106263 | |||||
| chrX:72106371
|
G | A | 3 | a0001c0001t0049g0019a0001c0001t0050g0119a0003c0004t0001g0121 | 3 | NA18944.hp1 NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.281-25708G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72106371 | ||||||
| chrX:72106398
|
TA | T | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25676delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106398 | |||||
| chrX:72106485
|
GGA | G | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25591_281-2559 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106485 | |||||
| chrX:72106493
|
A | AG | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25584dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106493 | |||||
| chrX:72106535
|
A | AC | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25542dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106535 | |||||
| chrX:72106649
|
T | A | 1 | a0001c0001t0057g0103 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.281-25430T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72106649 | ||||||
| chrX:72106735
|
TG | T | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25342delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106735 | |||||
| chrX:72106766
|
TG | T | 1 | a0003c0004t0006g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.281-25311delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72106766 | |||||
| chrX:72106826
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0066others(20): Show | 23 | HG00438.hp1 HG01069.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.281-25253G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72106826 | ||||||
| chrX:72106968
|
G | C | 4 | a0001c0001t0067g0148a0001c0003t0084g0150a0001c0020t0005g0012others(1): Show | 4 | HG02109.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-25111G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72106968 | ||||||
| chrX:72107250
|
C | T | 1 | a0001c0001t0014g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.281-24829C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72107250 | ||||||
| chrX:72107275
|
TTAAATAA others(1): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.281-24787_281-2478 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72107275 | |||||
| chrX:72107439
|
G | A | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-24640G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72107439 | ||||||
| chrX:72107500
|
T | A | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-24579T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72107500 | ||||||
| chrX:72107860
|
A | G | 8 | a0001c0001t0005g0091a0001c0001t0056g0092a0001c0001t0067g0148others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-24219A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72107860 | ||||||
| chrX:72107977
|
C | T | 8 | a0001c0001t0055g0068a0001c0003t0011g0155a0001c0003t0011g0156others(5): Show | 8 | HG02451.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-24102C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72107977 | ||||||
| chrX:72108019
|
G | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-24060G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72108019 | ||||||
| chrX:72108547
|
C | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-23532C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72108547 | ||||||
| chrX:72108680
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.281-23399C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72108680 | ||||||
| chrX:72108687
|
T | A | 1 | a0001c0001t0015g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281-23392T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72108687 | ||||||
| chrX:72108690
|
C | T | 1 | a0001c0020t0005g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-23389C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72108690 | ||||||
| chrX:72108899
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0100 | 2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.281-23180C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72108899 | ||||||
| chrX:72109072
|
C | T | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-23007C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109072 | ||||||
| chrX:72109123
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-22956G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109123 | ||||||
| chrX:72109181
|
C | T | 2 | a0001c0001t0019g0160a0001c0001t0019g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.281-22898C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109181 | ||||||
| chrX:72109470
|
G | A | 6 | a0001c0001t0067g0148a0001c0003t0030g0152a0001c0003t0034g0153others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-22609G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109470 | ||||||
| chrX:72109636
|
T | G | 1 | a0001c0001t0018g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281-22443T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109636 | ||||||
| chrX:72109710
|
G | A | 1 | a0004c0005t0082g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.281-22369G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109710 | ||||||
| chrX:72109717
|
T | G | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-22362T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109717 | ||||||
| chrX:72109823
|
T | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0004g0014others(18): Show | 21 | HG00438.hp1 HG01109.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-22256T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72109823 | ||||||
| chrX:72110034
|
G | A | 7 | a0001c0001t0055g0068a0001c0003t0011g0155a0001c0003t0011g0156others(4): Show | 7 | HG02451.hp2 HG02818.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-22045G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110034 | ||||||
| chrX:72110076
|
A | C | 1 | a0001c0001t0055g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-22003A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110076 | ||||||
| chrX:72110223
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.281-21856C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110223 | ||||||
| chrX:72110358
|
G | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0170a0002c0002t0002g0118others(6): Show | 9 | HG01433.hp1 HG02735.hp1 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-21721G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110358 | ||||||
| chrX:72110554
|
C | G | 1 | a0001c0001t0073g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-21525C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110554 | ||||||
| chrX:72110678
|
G | C | 2 | a0001c0001t0001g0138a0008c0017t0053g0059 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.281-21401G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110678 | ||||||
| chrX:72110724
|
TA | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(41): Show | 44 | HG00438.hp2 HG02015.hp1 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.281-21327delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAA | T | 11 | a0001c0001t0001g0004a0001c0001t0004g0014a0001c0001t0004g0066others(8): Show | 11 | HG00438.hp1 HG01358.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-21328_281-2132 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAA | T | 3 | a0001c0001t0014g0173a0001c0001t0047g0117a0001c0015t0032g0031 | 3 | HG02615.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.281-21329_281-2132 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAAA | T | 37 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.281-21330_281-2132 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAAAA | T | 20 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0015g0135others(17): Show | 20 | HG00738.hp1 HG01433.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-21331_281-2132 others(9): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAAAAA | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0074a0001c0001t0001g0099others(12): Show | 15 | HG01069.hp1 HG01169.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-21332_281-2132 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAAAAAA | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG00673.hp1 HG01167.hp1 HG02071.hp1 others(39): Show |
intron_variant | MODIFIER | c.281-21333_281-2132 others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAAAAAA others(1): Show |
T | 2 | a0001c0001t0001g0094a0001c0001t0022g0127 | 2 | HG02145.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.281-21334_281-2132 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110724
|
TAAAAAAA others(5): Show |
T | 1 | a0003c0004t0071g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.281-21338_281-2132 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72110724 | |||||
| chrX:72110746
|
A | C | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-21333A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72110746 | ||||||
| chrX:72111398
|
A | G | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-20681A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72111398 | ||||||
| chrX:72111506
|
A | T | 4 | a0001c0001t0016g0175a0001c0001t0046g0123a0001c0001t0047g0117others(1): Show | 4 | HG00642.hp1 HG01074.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-20573A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72111506 | ||||||
| chrX:72111836
|
A | G | 9 | a0001c0001t0001g0138a0001c0001t0005g0091a0001c0001t0056g0092others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-20243A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72111836 | ||||||
| chrX:72111877
|
A | G | 72 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0115others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.281-20202A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72111877 | ||||||
| chrX:72112028
|
AT | A | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.281-20048delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72112028 | |||||
| chrX:72112234
|
A | AT | 1 | a0002c0002t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-19844dupT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72112234 | |||||
| chrX:72112264
|
G | C | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-19815G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112264 | ||||||
| chrX:72112403
|
A | T | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.281-19676A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112403 | ||||||
| chrX:72112467
|
A | C | 1 | a0001c0001t0074g0142 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.281-19612A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112467 | ||||||
| chrX:72112473
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.281-19606C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112473 | ||||||
| chrX:72112616
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.281-19463T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112616 | ||||||
| chrX:72112846
|
C | T | 3 | a0001c0001t0051g0187a0001c0003t0070g0027a0001c0003t0084g0150 | 3 | HG02965.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-19233C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112846 | ||||||
| chrX:72112901
|
G | A | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-19178G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72112901 | ||||||
| chrX:72113016
|
A | G | 4 | a0001c0001t0073g0134a0001c0020t0005g0012a0009c0010t0052g0185others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-19063A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72113016 | ||||||
| chrX:72113194
|
G | T | 1 | a0001c0001t0037g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.281-18885G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72113194 | ||||||
| chrX:72113608
|
G | A | 1 | a0001c0001t0073g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-18471G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72113608 | ||||||
| chrX:72113837
|
G | A | 1 | a0001c0015t0032g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.281-18242G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72113837 | ||||||
| chrX:72114019
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-18060A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72114019 | ||||||
| chrX:72114035
|
C | T | 1 | a0012c0018t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.281-18044C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72114035 | ||||||
| chrX:72114482
|
A | T | 1 | a0001c0001t0072g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.281-17597A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72114482 | ||||||
| chrX:72114518
|
A | G | 63 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0094others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.281-17561A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72114518 | ||||||
| chrX:72114921
|
C | T | 1 | a0001c0001t0021g0006 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.281-17158C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72114921 | ||||||
| chrX:72115431
|
C | CG | 27 | a0001c0001t0001g0028a0001c0001t0001g0138a0001c0001t0003g0050others(24): Show | 27 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-16638dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115431 | |||||
| chrX:72115431
|
C | CGG | 51 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(48): Show | 51 | HG00621.hp1 HG00673.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.281-16639_281-1663 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115431 | |||||
| chrX:72115431
|
C | CGGG | 30 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0021others(27): Show | 30 | HG00438.hp2 HG02015.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.281-16640_281-1663 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115431 | |||||
| chrX:72115431
|
C | CGGGG | 7 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0033others(4): Show | 7 | HG02027.hp1 HG02155.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-16641_281-1663 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115431 | |||||
| chrX:72115431
|
C | CGGGGG | 5 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0009g0032others(2): Show | 5 | HG00438.hp1 HG03209.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-16642_281-1663 others(9): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115431 | |||||
| chrX:72115431
|
CG | C | 27 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0170others(24): Show | 27 | HG00609.hp1 HG00738.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-16638delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115431 | |||||
| chrX:72115434
|
G | GGA | 2 | a0001c0001t0083g0113a0003c0004t0006g0112 | 2 | NA18967.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.281-16644_281-1664 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115434 | |||||
| chrX:72115439
|
G | GGGT | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-16638_281-1663 others(7): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72115439 | |||||
| chrX:72115557
|
T | C | 4 | a0001c0001t0001g0065a0002c0002t0002g0124a0002c0002t0077g0183others(1): Show | 4 | HG04228.hp1 NA18989.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-16522T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72115557 | ||||||
| chrX:72115830
|
G | A | 2 | a0001c0003t0070g0027a0001c0003t0084g0150 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-16249G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72115830 | ||||||
| chrX:72116067
|
C | T | 1 | a0001c0001t0014g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.281-16012C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116067 | ||||||
| chrX:72116289
|
T | C | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-15790T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116289 | ||||||
| chrX:72116433
|
T | C | 1 | a0001c0001t0080g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.281-15646T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116433 | ||||||
| chrX:72116506
|
T | C | 2 | a0001c0001t0014g0173a0001c0001t0026g0172 | 2 | HG01192.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.281-15573T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116506 | ||||||
| chrX:72116689
|
C | A | 36 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.281-15390C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116689 | ||||||
| chrX:72116787
|
A | AGGGGGT | 36 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.281-15290_281-1528 others(10): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72116787 | |||||
| chrX:72116800
|
G | C | 3 | a0001c0001t0072g0038a0001c0001t0083g0113a0003c0004t0006g0112 | 3 | NA18967.hp1 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.281-15279G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116800 | ||||||
| chrX:72116889
|
G | A | 3 | a0001c0001t0072g0038a0001c0001t0083g0113a0003c0004t0006g0112 | 3 | NA18967.hp1 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.281-15190G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72116889 | ||||||
| chrX:72117196
|
G | A | 2 | a0001c0003t0070g0027a0001c0003t0084g0150 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-14883G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72117196 | ||||||
| chrX:72117276
|
CAT | C | 2 | a0001c0001t0004g0066a0001c0001t0004g0128 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.281-14801_281-1480 others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72117276 | |||||
| chrX:72117602
|
G | A | 29 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0051g0187others(26): Show | 29 | HG00738.hp1 HG01433.hp1 HG02486.hp1 others(26): Show |
intron_variant | MODIFIER | c.281-14477G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72117602 | ||||||
| chrX:72117631
|
G | A | 2 | a0001c0001t0009g0032a0001c0001t0020g0139 | 2 | NA18994.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.281-14448G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72117631 | ||||||
| chrX:72117818
|
T | TTTTA | 66 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0089others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.281-14223_281-1422 others(8): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72117818 | |||||
| chrX:72117818
|
T | TTTTATTT others(1): Show |
27 | a0001c0001t0001g0065a0001c0001t0001g0115a0001c0001t0001g0177others(24): Show | 27 | HG00738.hp1 HG01256.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-14227_281-1422 others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72117818 | |||||
| chrX:72117818
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0005g0091a0001c0011t0003g0013a0002c0002t0002g0145 | 3 | HG01109.hp1 HG02602.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.281-14231_281-1422 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72117818 | |||||
| chrX:72117818
|
T | TTTTATTT others(9): Show |
1 | a0002c0002t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.281-14235_281-1422 others(20): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72117818 | |||||
| chrX:72117822
|
A | T | 1 | a0001c0001t0056g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.281-14257A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72117822 | ||||||
| chrX:72117853
|
T | TATTTATT others(5): Show |
2 | a0001c0003t0070g0027a0001c0003t0084g0150 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.281-14220_281-1421 others(16): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72117853 | |||||
| chrX:72118032
|
T | C | 39 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.281-14047T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72118032 | ||||||
| chrX:72118266
|
T | C | 1 | a0001c0001t0048g0168 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.281-13813T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72118266 | ||||||
| chrX:72119015
|
A | G | 1 | a0001c0019t0054g0070 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-13064A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72119015 | ||||||
| chrX:72119180
|
A | G | 179 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(176): Show | 179 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.281-12899A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72119180 | ||||||
| chrX:72119795
|
T | C | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-12284T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72119795 | ||||||
| chrX:72119817
|
C | T | 2 | a0001c0001t0055g0068a0001c0001t0057g0103 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.281-12262C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72119817 | ||||||
| chrX:72119847
|
A | G | 8 | a0001c0001t0005g0091a0001c0001t0005g0096a0001c0001t0005g0146others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-12232A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72119847 | ||||||
| chrX:72120144
|
A | G | 14 | a0001c0001t0001g0126a0001c0001t0004g0014a0001c0001t0004g0066others(11): Show | 14 | HG01358.hp1 HG02055.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-11935A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72120144 | ||||||
| chrX:72120172
|
G | A | 1 | a0002c0002t0013g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.281-11907G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72120172 | ||||||
| chrX:72120582
|
T | C | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-11497T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72120582 | ||||||
| chrX:72120737
|
T | C | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.281-11342T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72120737 | ||||||
| chrX:72121671
|
G | A | 3 | a0001c0001t0005g0096a0001c0001t0005g0146a0001c0020t0005g0012 | 3 | HG02258.hp1 HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.281-10408G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72121671 | ||||||
| chrX:72121861
|
A | G | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(170): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.281-10218A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72121861 | ||||||
| chrX:72122058
|
T | C | 30 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(27): Show | 30 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.281-10021T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122058 | ||||||
| chrX:72122131
|
C | T | 34 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0005g0091others(31): Show | 34 | HG00738.hp1 HG01109.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.281-9948C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122131 | ||||||
| chrX:72122156
|
A | G | 179 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(176): Show | 179 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.281-9923A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122156 | ||||||
| chrX:72122177
|
A | G | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(184): Show | 187 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.281-9902A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122177 | ||||||
| chrX:72122213
|
C | A | 3 | a0001c0001t0073g0134a0001c0003t0028g0159a0001c0003t0029g0149 | 3 | HG02280.hp2 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.281-9866C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122213 | ||||||
| chrX:72122476
|
G | A | 4 | a0001c0001t0015g0049a0001c0001t0015g0135a0001c0001t0055g0068others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-9603G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122476 | ||||||
| chrX:72122570
|
AT | A | 25 | a0001c0001t0001g0065a0001c0001t0001g0170a0002c0002t0002g0039others(22): Show | 25 | HG00738.hp1 HG01433.hp1 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-9507delT | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72122570 | |||||
| chrX:72122745
|
C | G | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(77): Show | 80 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.281-9334C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122745 | ||||||
| chrX:72122749
|
T | C | 67 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0003g0016others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.281-9330T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72122749 | ||||||
| chrX:72123210
|
G | A | 6 | a0001c0003t0011g0155a0001c0003t0011g0156a0001c0003t0030g0152others(3): Show | 6 | HG02559.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-8869G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72123210 | ||||||
| chrX:72123351
|
C | T | 1 | a0001c0003t0036g0054 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.281-8728C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72123351 | ||||||
| chrX:72123583
|
C | T | 34 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0005g0091others(31): Show | 34 | HG00738.hp1 HG01109.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.281-8496C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72123583 | ||||||
| chrX:72123634
|
G | A | 1 | a0010c0016t0075g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-8445G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72123634 | ||||||
| chrX:72123685
|
G | A | 34 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0005g0091others(31): Show | 34 | HG00738.hp1 HG01109.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.281-8394G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72123685 | ||||||
| chrX:72124138
|
T | C | 8 | a0001c0001t0005g0091a0001c0001t0005g0096a0001c0001t0005g0146others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-7941T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124138 | ||||||
| chrX:72124140
|
CCATTAAG others(3): Show |
C | 8 | a0001c0001t0005g0091a0001c0001t0005g0096a0001c0001t0005g0146others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-7938_281-7929d others(12): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124140 | ||||||
| chrX:72124151
|
G | T | 8 | a0001c0001t0005g0091a0001c0001t0005g0096a0001c0001t0005g0146others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-7928G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124151 | ||||||
| chrX:72124453
|
T | C | 50 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.281-7626T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124453 | ||||||
| chrX:72124738
|
T | C | 30 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(27): Show | 30 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.281-7341T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124738 | ||||||
| chrX:72124876
|
TCTTC | T | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-7183_281-7180d others(6): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72124876 | |||||
| chrX:72124910
|
G | A | 27 | a0001c0001t0001g0065a0001c0001t0001g0170a0002c0002t0002g0039others(24): Show | 27 | HG00738.hp1 HG01433.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-7169G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124910 | ||||||
| chrX:72124917
|
T | G | 27 | a0001c0001t0001g0065a0001c0001t0001g0170a0002c0002t0002g0039others(24): Show | 27 | HG00738.hp1 HG01433.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-7162T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72124917 | ||||||
| chrX:72125014
|
T | C | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(170): Show | 173 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.281-7065T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125014 | ||||||
| chrX:72125070
|
GTCTGTGA others(2): Show |
G | 66 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0003g0016others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.281-7008_281-7000d others(11): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125070 | ||||||
| chrX:72125080
|
C | A | 66 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0003g0016others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.281-6999C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125080 | ||||||
| chrX:72125081
|
T | A | 66 | a0001c0001t0001g0065a0001c0001t0001g0170a0001c0001t0003g0016others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.281-6998T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125081 | ||||||
| chrX:72125112
|
A | G | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-6967A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125112 | ||||||
| chrX:72125491
|
G | A | 50 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.281-6588G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125491 | ||||||
| chrX:72125533
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.281-6546A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125533 | ||||||
| chrX:72125721
|
A | C | 50 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.281-6358A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125721 | ||||||
| chrX:72125963
|
G | A | 4 | a0002c0002t0002g0064a0002c0002t0007g0077a0002c0002t0007g0106others(1): Show | 4 | HG03239.hp1 HG03654.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-6116G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72125963 | ||||||
| chrX:72126528
|
C | G | 1 | a0004c0005t0043g0061 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.281-5551C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72126528 | ||||||
| chrX:72126573
|
G | GA | 49 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.281-5494dupA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72126573 | |||||
| chrX:72126573
|
G | GAA | 1 | a0006c0007t0013g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.281-5495_281-5494d others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72126573 | |||||
| chrX:72126573
|
GA | G | 1 | a0001c0001t0073g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-5494delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72126573 | |||||
| chrX:72126587
|
T | G | 1 | a0001c0001t0066g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-5492T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72126587 | ||||||
| chrX:72126771
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0144 | 2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.281-5308G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72126771 | ||||||
| chrX:72127035
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0074others(4): Show | 7 | HG02071.hp1 HG02132.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-5044G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72127035 | ||||||
| chrX:72127053
|
T | C | 43 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.281-5026T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72127053 | ||||||
| chrX:72127410
|
C | T | 1 | a0001c0001t0046g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.281-4669C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72127410 | ||||||
| chrX:72127584
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.281-4495G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72127584 | ||||||
| chrX:72127630
|
G | GCCTCGAA others(13): Show |
42 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.281-4425_281-4406d others(22): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72127630 | |||||
| chrX:72127748
|
A | AC | 1 | a0001c0001t0001g0074 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.281-4330dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72127748 | |||||
| chrX:72128105
|
T | C | 43 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.281-3974T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72128105 | ||||||
| chrX:72128147
|
T | C | 13 | a0001c0001t0004g0014a0001c0001t0004g0066a0001c0001t0004g0128others(10): Show | 13 | HG01358.hp1 HG02055.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.281-3932T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72128147 | ||||||
| chrX:72128750
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.281-3329C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72128750 | ||||||
| chrX:72128987
|
G | A | 28 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-3092G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72128987 | ||||||
| chrX:72129267
|
G | A | 3 | a0001c0001t0005g0096a0001c0001t0005g0146a0001c0020t0005g0012 | 3 | HG02258.hp1 HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.281-2812G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129267 | ||||||
| chrX:72129293
|
A | C | 43 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.281-2786A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129293 | ||||||
| chrX:72129512
|
A | G | 8 | a0001c0001t0005g0091a0001c0001t0005g0096a0001c0001t0005g0146others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-2567A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129512 | ||||||
| chrX:72129578
|
C | T | 1 | a0002c0002t0002g0157 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.281-2501C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129578 | ||||||
| chrX:72129738
|
C | A | 2 | a0001c0001t0049g0019a0001c0001t0050g0119 | 2 | NA18959.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.281-2341C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129738 | ||||||
| chrX:72129850
|
C | T | 1 | a0001c0019t0054g0070 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-2229C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129850 | ||||||
| chrX:72129877
|
G | T | 1 | a0001c0003t0012g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-2202G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129877 | ||||||
| chrX:72129903
|
G | A | 28 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-2176G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129903 | ||||||
| chrX:72129924
|
T | C | 43 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.281-2155T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129924 | ||||||
| chrX:72129957
|
G | C | 3 | a0001c0001t0037g0154a0001c0001t0038g0158a0001c0001t0039g0151 | 3 | HG02451.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.281-2122G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72129957 | ||||||
| chrX:72130143
|
C | T | 8 | a0001c0001t0005g0091a0001c0001t0005g0096a0001c0001t0005g0146others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-1936C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72130143 | ||||||
| chrX:72130283
|
T | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0017others(39): Show | 42 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.281-1796T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72130283 | ||||||
| chrX:72130723
|
TG | T | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-1354delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72130723 | |||||
| chrX:72130994
|
C | CG | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-1081dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72130994 | |||||
| chrX:72131109
|
A | AG | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.281-965dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72131109 | |||||
| chrX:72131157
|
C | CG | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-917dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72131157 | |||||
| chrX:72131449
|
T | C | 3 | a0001c0001t0037g0154a0001c0001t0038g0158a0001c0001t0039g0151 | 3 | HG02451.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.281-630T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131449 | ||||||
| chrX:72131487
|
C | A | 5 | a0001c0001t0051g0187a0001c0001t0055g0068a0001c0001t0056g0092others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-592C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131487 | ||||||
| chrX:72131593
|
A | G | 43 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.281-486A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131593 | ||||||
| chrX:72131611
|
A | AG | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-466dupG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72131611 | |||||
| chrX:72131646
|
G | A | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-433G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131646 | ||||||
| chrX:72131669
|
C | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.281-410C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131669 | ||||||
| chrX:72131752
|
A | AC | 2 | a0001c0001t0001g0026a0011c0009t0001g0176 | 2 | NA18977.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.281-325dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72131752 | |||||
| chrX:72131796
|
C | T | 43 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.281-283C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131796 | ||||||
| chrX:72131805
|
C | T | 5 | a0001c0001t0051g0187a0001c0001t0055g0068a0001c0001t0056g0092others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-274C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131805 | ||||||
| chrX:72131827
|
C | A | 5 | a0001c0001t0051g0187a0001c0001t0055g0068a0001c0001t0056g0092others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-252C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72131827 | ||||||
| chrX:72131850
|
C | CCGGG | 2 | a0001c0001t0015g0135a0001c0001t0041g0044 | 2 | HG02155.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.281-215_281-212dup others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72131850 | |||||
| chrX:72131966
|
T | TC | 3 | a0001c0001t0001g0026a0001c0001t0062g0036a0006c0007t0013g0090 | 3 | HG02055.hp1 HG04199.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.281-107dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 72131966 | |||||
| chrX:72132022
|
C | G | 7 | a0001c0001t0067g0148a0001c0003t0011g0155a0001c0003t0011g0156others(4): Show | 7 | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-57C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | chrX | 72132022 | ||||||
| chrX:72132271
|
A | G | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436+37A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72132271 | ||||||
| chrX:72132337
|
C | G | 50 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.436+103C>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72132337 | ||||||
| chrX:72132419
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.436+185G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72132419 | ||||||
| chrX:72132489
|
G | C | 1 | a0001c0001t0067g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.436+255G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72132489 | ||||||
| chrX:72132504
|
T | C | 50 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.436+270T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72132504 | ||||||
| chrX:72132671
|
A | G | 31 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.436+437A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72132671 | ||||||
| chrX:72133325
|
G | A | 8 | a0002c0002t0002g0060a0002c0002t0002g0086a0002c0002t0002g0101others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-766G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72133325 | ||||||
| chrX:72133553
|
AC | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.437-536delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 72133553 | |||||
| chrX:72133609
|
C | T | 1 | a0008c0017t0053g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.437-482C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72133609 | ||||||
| chrX:72133808
|
C | T | 30 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(27): Show | 30 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.437-283C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72133808 | ||||||
| chrX:72133856
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.437-235C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 2/7 | chrX | 72133856 | ||||||
| chrX:72134834
|
G | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(83): Show | 86 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.760+130G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72134834 | ||||||
| chrX:72135061
|
C | T | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(126): Show | 129 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.760+357C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72135061 | ||||||
| chrX:72135142
|
T | C | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.760+438T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72135142 | ||||||
| chrX:72135432
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.760+728C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72135432 | ||||||
| chrX:72135872
|
C | T | 2 | a0002c0002t0077g0183a0002c0002t0079g0165 | 2 | NA18989.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.760+1168C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72135872 | ||||||
| chrX:72135984
|
C | T | 2 | a0002c0002t0002g0064a0002c0002t0007g0129 | 2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.761-1110C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72135984 | ||||||
| chrX:72136079
|
C | T | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(164): Show | 167 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.761-1015C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136079 | ||||||
| chrX:72136122
|
G | A | 33 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.761-972G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136122 | ||||||
| chrX:72136171
|
A | C | 18 | a0001c0001t0004g0014a0001c0001t0004g0066a0001c0001t0004g0116others(15): Show | 18 | HG00621.hp1 HG01358.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.761-923A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136171 | ||||||
| chrX:72136219
|
T | TC | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.761-872dupC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 72136219 | |||||
| chrX:72136273
|
T | A | 13 | a0001c0001t0004g0014a0001c0001t0004g0066a0001c0001t0004g0116others(10): Show | 13 | HG00621.hp1 HG01358.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-821T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136273 | ||||||
| chrX:72136314
|
A | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.761-780A>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136314 | ||||||
| chrX:72136625
|
C | T | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.761-469C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136625 | ||||||
| chrX:72136881
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.761-213G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 4/7 | chrX | 72136881 | ||||||
| chrX:72137243
|
G | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.892+18G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72137243 | ||||||
| chrX:72137310
|
G | T | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.892+85G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72137310 | ||||||
| chrX:72137434
|
CG | C | 1 | a0001c0001t0024g0001 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.892+212delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 72137434 | |||||
| chrX:72137595
|
G | T | 1 | a0002c0002t0002g0105 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.892+370G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72137595 | ||||||
| chrX:72137717
|
T | C | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.892+492T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72137717 | ||||||
| chrX:72137964
|
C | T | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.893-477C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72137964 | ||||||
| chrX:72137999
|
T | G | 1 | a0001c0015t0032g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.893-442T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72137999 | ||||||
| chrX:72138224
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG00609.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-217C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 5/7 | chrX | 72138224 | ||||||
| chrX:72140818
|
G | C | 1 | a0009c0010t0052g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3223+47G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72140818 | ||||||
| chrX:72141015
|
C | T | 33 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.3223+244C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141015 | ||||||
| chrX:72141084
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0009g0184others(4): Show | 7 | NA18965.hp1 NA18967.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.3223+313G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141084 | ||||||
| chrX:72141225
|
T | G | 1 | a0001c0001t0051g0187 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3223+454T>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141225 | ||||||
| chrX:72141341
|
T | A | 2 | a0001c0001t0010g0084a0004c0005t0001g0088 | 2 | NA18995.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.3223+570T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141341 | ||||||
| chrX:72141381
|
G | A | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3223+610G>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141381 | ||||||
| chrX:72141568
|
C | T | 31 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.3224-664C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141568 | ||||||
| chrX:72141635
|
T | C | 6 | a0001c0003t0011g0155a0001c0003t0011g0156a0001c0003t0030g0152others(3): Show | 6 | HG02559.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3224-597T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141635 | ||||||
| chrX:72141780
|
T | C | 6 | a0001c0003t0011g0155a0001c0003t0011g0156a0001c0003t0030g0152others(3): Show | 6 | HG02559.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3224-452T>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141780 | ||||||
| chrX:72141980
|
C | T | 7 | a0001c0003t0011g0155a0001c0003t0011g0156a0001c0003t0030g0152others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.3224-252C>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72141980 | ||||||
| chrX:72142099
|
A | G | 25 | a0002c0002t0002g0039a0002c0002t0002g0056a0002c0002t0002g0060others(22): Show | 25 | HG00738.hp1 HG02486.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.3224-133A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 6/7 | chrX | 72142099 | ||||||
| chrX:72142434
|
TC | T | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+72delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142434 | |||||
| chrX:72142455
|
TA | T | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+95delA | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142455 | |||||
| chrX:72142472
|
AAT | A | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+109_3356+110d others(4): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72142472 | ||||||
| chrX:72142476
|
A | T | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+112A>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72142476 | ||||||
| chrX:72142604
|
G | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(32): Show | 35 | HG00438.hp2 HG02015.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.3356+240G>C | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72142604 | ||||||
| chrX:72142608
|
AG | A | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+246delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142608 | |||||
| chrX:72142648
|
GC | G | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+288delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142648 | |||||
| chrX:72142686
|
TC | T | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3356+324delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142686 | |||||
| chrX:72142831
|
TG | T | 1 | a0001c0001t0023g0055 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3357-418delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142831 | |||||
| chrX:72142869
|
T | A | 1 | a0001c0001t0039g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3357-384T>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72142869 | ||||||
| chrX:72142878
|
A | G | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3357-375A>G | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72142878 | ||||||
| chrX:72142935
|
TC | T | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3357-314delC | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72142935 | |||||
| chrX:72143015
|
AG | A | 1 | a0011c0009t0001g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3357-236delG | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 72143015 | |||||
| chrX:72143052
|
C | A | 2 | a0001c0003t0028g0159a0001c0003t0029g0149 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3357-201C>A | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72143052 | ||||||
| chrX:72143054
|
G | T | 31 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0097others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.3357-199G>T | NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 7/7 | chrX | 72143054 |