Item | Value |
---|---|
geneid | 54413 |
ensemblid | ENSG00000196338.15 |
hgncid | 14289 |
symbol | NLGN3 |
name | neuroligin 3 |
refseq_nuc | NM_181303.2 |
refseq_prot | NP_851820.1 |
ensembl_nuc | ENST00000358741.4 |
ensembl_prot | ENSP00000351591.4 |
mane_status | MANE Select |
chr | chrX |
start | 71144841 |
end | 71171201 |
strand | + |
ver | v1.2 |
region | chrX:71144841-71171201 |
region5000 | chrX:71139841-71176201 |
regionname0 | NLGN3_chrX_71144841_71171201 |
regionname5000 | NLGN3_chrX_71139841_71176201 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 848 | 275 | 81 | 61 | 93 | 9 | 29 | 72 | NLGN3_chrX_71139841_71176201 | NLGN3 | MWLRL others(843): Show |
chrX | 71139841 | 71176201 |
a0002 | 0/0 | 848 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | MWLRL others(843): Show |
chrX | 71139841 | 71176201 |
a0003 | 0/0 | 848 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | MWLRL others(843): Show |
chrX | 71139841 | 71176201 |
a0004 | 0/0 | 848 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | MWLRL others(843): Show |
chrX | 71139841 | 71176201 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2544 | 268 | 76 | 61 | 92 | 9 | 28 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0001c0002 | 0/0 | 2544 | 4 | 4 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0001c0004 | 0/0 | 2544 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0001c0006 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0001c0007 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0002c0008 | 0/0 | 2544 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0003c0003 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 | ||
a0004c0005 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | ATGTG others(2539): Show |
chrX | 71139841 | 71176201 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3975 | 172 | 27 | 35 | 77 | 9 | 22 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0002 | 0/0 | 3977 | 65 | 35 | 21 | 4 | 0 | 5 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3972): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0003 | 0/0 | 3979 | 11 | 9 | 2 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3974): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0004 | 0/0 | 3976 | 7 | 0 | 1 | 6 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3971): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0005 | 0/0 | 3978 | 5 | 5 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3973): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0006 | 0/0 | 3976 | 3 | 0 | 1 | 2 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3971): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0007 | 0/0 | 3975 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0008 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0009 | 0/0 | 3974 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3969): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0010 | 0/0 | 3974 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3969): Show |
chrX | 71139841 | 71176201 |
a0001c0001t0011 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0002t0001 | 0/0 | 3975 | 4 | 4 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0004t0001 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0006t0001 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0001c0007t0002 | 0/0 | 3977 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3972): Show |
chrX | 71139841 | 71176201 |
a0002c0008t0001 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
a0003c0003t0002 | 0/0 | 3977 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3972): Show |
chrX | 71139841 | 71176201 |
a0004c0005t0001 | 0/0 | 3975 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | GCGGG others(3970): Show |
chrX | 71139841 | 71176201 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 35 | 0 | 10 | 18 | 2 | 4 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0004 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0004g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0001c0007t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0002c0008t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0003c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
a0004c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02071 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02165 | hp1 | a0001 | c0001 | t0009 | g0109 | EAS | CDX | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0073 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02523 | hp1 | a0001 | c0006 | t0001 | g0019 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02683 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02723 | hp1 | a0001 | c0007 | t0002 | g0114 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03017 | hp1 | a0002 | c0008 | t0001 | g0118 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03041 | hp1 | a0003 | c0003 | t0002 | g0012 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03834 | hp2 | a0001 | c0001 | t0010 | g0140 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0074 | AFR | YRI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | YRI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18941 | hp1 | a0004 | c0005 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19006 | hp1 | a0001 | c0001 | t0008 | g0048 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | LWK | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ASW | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | USA | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | USA | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | LWK | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0067 | REF | REF | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NLGN3_chrX_71139841_71176201 | NLGN3 | chrX | 71139841 | 71176201 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71155220 | G | A | 1 | a0003 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.584G>A | p.Arg195Gln | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/8 | 908/3975 | 584/2547 | 195/848 | chrX | 71155220 | |||
chrX:71164212 | G | A | 1 | a0004 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.797G>A | p.Arg266His | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/8 | 1121/3975 | 797/2547 | 266/848 | chrX | 71164212 | |||
chrX:71169882 | G | A | 1 | a0002 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.2332G>A | p.Gly778Ser | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 2656/3975 | 2332/2547 | 778/848 | chrX | 71169882 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71155230 | T | C | 1 | a0001c0004 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.594T>C | p.Gly198Gly | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/8 | 918/3975 | 594/2547 | 198/848 | chrX | 71155230 | |||
chrX:71167795 | G | A | 1 | a0001c0006 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1698G>A | p.Lys566Lys | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/8 | 2022/3975 | 1698/2547 | 566/848 | chrX | 71167795 | |||
chrX:71169494 | G | A | 1 | a0001c0007 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1944G>A | p.Pro648Pro | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 2268/3975 | 1944/2547 | 648/848 | chrX | 71169494 | |||
chrX:71169800 | C | T | 1 | a0001c0002 | 4 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.2250C>T | p.Ala750Ala | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 2574/3975 | 2250/2547 | 750/848 | chrX | 71169800 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71147690 | T | C | 1 | a0001c0001t0007 | 1 | HG01106.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 2/8 | 60 | chrX | 71147690 | ||||||
chrX:71170133 | T | C | 1 | a0001c0001t0008 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 36 | chrX | 71170133 | ||||||
chrX:71170157 | G | GCA | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(2): Show |
79 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*80_*81dupAC | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 82 | INFO_REALIGN_3_PRIME | chrX | 71170157 | |||||
chrX:71170157 | G | GCACA | 1 | a0001c0001t0003 | 11 | HG01255.hp1 HG01884.hp1 HG01993.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*78_*81dupACAC | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 82 | INFO_REALIGN_3_PRIME | chrX | 71170157 | |||||
chrX:71170333 | C | T | 1 | a0001c0001t0011 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 236 | chrX | 71170333 | ||||||
chrX:71170578 | T | C | 1 | a0001c0001t0008 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 481 | chrX | 71170578 | ||||||
chrX:71171057 | G | A | 1 | a0001c0001t0009 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 960 | chrX | 71171057 | ||||||
chrX:71171077 | G | GT | 2 | a0001c0001t0005 a0001c0001t0006 |
8 | HG01175.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*995dupT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 996 | INFO_REALIGN_3_PRIME | chrX | 71171077 | |||||
chrX:71171077 | GT | G | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0010 |
9 | HG01496.hp1 HG02080.hp1 HG02165.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*995delT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 8/8 | 995 | INFO_REALIGN_3_PRIME | chrX | 71171077 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:71145054 | C | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0133 others(55): Show |
75 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-201+90C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145054 | |||||||
chrX:71145055 | C | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0133 others(55): Show |
75 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-201+91C>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145055 | |||||||
chrX:71145113 | G | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0033 |
3 | HG01069.hp1 HG01071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-201+149G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145113 | |||||||
chrX:71145136 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
174 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(171): Show |
intron_variant | MODIFIER | c.-201+172C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145136 | |||||||
chrX:71145138 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
174 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(171): Show |
intron_variant | MODIFIER | c.-201+174T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145138 | |||||||
chrX:71145414 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-201+450C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145414 | |||||||
chrX:71145436 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0157 others(32): Show |
52 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-201+472C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145436 | |||||||
chrX:71145595 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(24): Show |
35 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-201+631G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145595 | |||||||
chrX:71145767 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-201+803A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71145767 | |||||||
chrX:71146124 | T | TTC | 5 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG01891.hp2 HG01993.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-201+1189_-201+119 others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146124 | ||||||
chrX:71146124 | T | TTCTC | 3 | a0001c0001t0001g0066 a0001c0001t0002g0030 a0001c0001t0002g0131 |
4 | HG00609.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-201+1187_-201+119 others(8): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146124 | ||||||
chrX:71146124 | TTC | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0134 others(1): Show |
5 | HG01175.hp2 HG01261.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-201+1189_-201+119 others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146124 | ||||||
chrX:71146124 | TTCTC | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0133 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-201+1187_-201+119 others(8): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146124 | ||||||
chrX:71146124 | TTCTCTC | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0033 |
3 | HG01167.hp1 HG01169.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-201+1185_-201+119 others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146124 | ||||||
chrX:71146145 | TCTCTCTC others(3): Show |
T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0068 |
3 | HG01069.hp1 HG01071.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-201+1183_-201+119 others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146145 | ||||||
chrX:71146145 | TCTCTCTC others(5): Show |
T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0070 others(16): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-201+1183_-201+119 others(16): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146145 | ||||||
chrX:71146145 | TCTCTCTC others(9): Show |
T | 1 | a0001c0002t0001g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-201+1183_-201+119 others(20): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146145 | ||||||
chrX:71146145 | TCTCTCTC others(11): Show |
T | 2 | a0001c0001t0001g0086 a0001c0001t0002g0085 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-201+1183_-201+120 others(22): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146145 | ||||||
chrX:71146147 | TCTCTCTC others(5): Show |
T | 1 | a0001c0001t0005g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-201+1185_-201+119 others(16): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146147 | ||||||
chrX:71146149 | TCTCTCAC others(3): Show |
T | 2 | a0001c0001t0002g0132 a0001c0002t0001g0116 |
2 | HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-201+1187_-201+119 others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146149 | ||||||
chrX:71146151 | T | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0043 |
4 | HG00735.hp1 HG01074.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-201+1187T>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146151 | |||||||
chrX:71146153 | T | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(8): Show |
15 | HG00735.hp1 HG01074.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-201+1189T>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146153 | |||||||
chrX:71146153 | T | TCTCTCA | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0002g0128 others(2): Show |
5 | HG02280.hp1 HG03486.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-201+1190_-201+119 others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146153 | ||||||
chrX:71146155 | A | T | 21 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0135 others(18): Show |
21 | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.-201+1191A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146155 | |||||||
chrX:71146156 | CACACACA others(9): Show |
C | 4 | a0001c0001t0001g0157 a0001c0001t0003g0005 a0001c0001t0003g0155 others(1): Show |
8 | HG01884.hp1 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-201+1208_-201+122 others(20): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146156 | ||||||
chrX:71146157 | A | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG00738.hp1 HG01891.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-201+1193A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146157 | |||||||
chrX:71146159 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-201+1195A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146159 | |||||||
chrX:71146160 | CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG01891.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-201+1208_-201+121 others(16): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146160 | ||||||
chrX:71146161 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-201+1197A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146161 | |||||||
chrX:71146162 | CACACACA others(3): Show |
C | 1 | a0001c0001t0002g0158 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-201+1208_-201+121 others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146162 | ||||||
chrX:71146163 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-201+1199A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146163 | |||||||
chrX:71146164 | CACACACA others(1): Show |
C | 13 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0162 others(10): Show |
17 | HG00639.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-201+1208_-201+121 others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146164 | ||||||
chrX:71146166 | CACACAG | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0105 others(15): Show |
22 | HG00673.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-201+1208_-201+121 others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146166 | ||||||
chrX:71146168 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-201+1204C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146168 | |||||||
chrX:71146168 | CACAG | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0120 others(26): Show |
38 | HG00735.hp2 HG00741.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.-201+1208_-201+121 others(8): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146168 | ||||||
chrX:71146170 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0006g0010 |
4 | HG01175.hp2 HG01261.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-201+1206C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146170 | |||||||
chrX:71146170 | CAG | C | 9 | a0001c0001t0001g0061 a0001c0001t0001g0117 a0001c0001t0001g0141 others(6): Show |
9 | HG01358.hp1 HG02056.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.-201+1208_-201+120 others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146170 | ||||||
chrX:71146172 | G | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(54): Show |
71 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-201+1208G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146172 | |||||||
chrX:71146172 | G | GAC | 12 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(9): Show |
16 | HG00741.hp2 HG02027.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.-201+1256_-201+125 others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | G | GACAC | 15 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(12): Show |
19 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.-201+1254_-201+125 others(8): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | G | GACACAC | 16 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(13): Show |
23 | HG00323.hp2 HG01433.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.-201+1252_-201+125 others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | G | GACACACA others(1): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0038 others(3): Show |
12 | HG00733.hp1 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.-201+1250_-201+125 others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | G | GACACACA others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0044 |
4 | HG01496.hp2 HG02683.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-201+1248_-201+125 others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | G | GACACACA others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0003g0063 |
3 | HG01993.hp1 NA18964.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-201+1246_-201+125 others(16): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | G | GACACACA others(9): Show |
1 | a0001c0001t0001g0066 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-201+1242_-201+125 others(20): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | GAC | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0059 others(1): Show |
5 | HG00280.hp1 HG03225.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-201+1256_-201+125 others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | GACAC | G | 7 | a0001c0001t0001g0007 a0001c0001t0002g0025 a0001c0001t0002g0092 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-201+1254_-201+125 others(8): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0001 a0001c0001t0005g0138 a0001c0001t0006g0139 |
3 | HG01978.hp2 HG02109.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-201+1250_-201+125 others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146172 | GACACACA others(3): Show |
G | 1 | a0001c0001t0002g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-201+1248_-201+125 others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146172 | ||||||
chrX:71146174 | C | G | 6 | a0001c0001t0001g0065 a0001c0001t0001g0127 a0001c0001t0001g0133 others(3): Show |
6 | HG02622.hp2 HG03486.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-201+1210C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146174 | |||||||
chrX:71146176 | C | G | 13 | a0001c0001t0001g0061 a0001c0001t0001g0090 a0001c0001t0001g0122 others(10): Show |
15 | HG01358.hp1 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-201+1212C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146176 | |||||||
chrX:71146178 | C | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0117 others(15): Show |
23 | HG00741.hp1 HG01256.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.-201+1214C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146178 | |||||||
chrX:71146180 | C | G | 35 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0032 others(32): Show |
44 | HG00673.hp1 HG00735.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.-201+1216C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146180 | |||||||
chrX:71146182 | C | G | 16 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0105 others(13): Show |
21 | HG00639.hp2 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-201+1218C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146182 | |||||||
chrX:71146184 | C | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0102 a0001c0001t0002g0103 others(1): Show |
4 | HG01361.hp2 HG02074.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-201+1220C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146184 | |||||||
chrX:71146186 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(14): Show |
25 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-201+1222C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146186 | |||||||
chrX:71146188 | C | G | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-201+1224C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146188 | |||||||
chrX:71146190 | C | G | 5 | a0001c0001t0001g0157 a0001c0001t0003g0005 a0001c0001t0003g0155 others(2): Show |
9 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-201+1226C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146190 | |||||||
chrX:71146192 | C | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0135 a0001c0001t0002g0085 |
3 | HG02280.hp2 HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-201+1228C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146192 | |||||||
chrX:71146364 | GGTGTGCG others(3): Show |
G | 2 | a0001c0001t0002g0069 a0001c0001t0005g0087 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-200-1168_-200-115 others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 71146364 | ||||||
chrX:71146838 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-200-712G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71146838 | |||||||
chrX:71147090 | G | T | 3 | a0001c0001t0001g0086 a0001c0001t0002g0085 a0001c0002t0001g0084 |
3 | HG02280.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-200-460G>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71147090 | |||||||
chrX:71147196 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(130): Show |
166 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(163): Show |
intron_variant | MODIFIER | c.-200-354A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71147196 | |||||||
chrX:71147478 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
163 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.-200-72A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 1/7 | chrX | 71147478 | |||||||
chrX:71148359 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.457+153C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 2/7 | chrX | 71148359 | |||||||
chrX:71148758 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.458-88G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 2/7 | chrX | 71148758 | |||||||
chrX:71148775 | T | TG | 5 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
8 | NA18940.hp1 NA18955.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-65dupG | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 71148775 | ||||||
chrX:71149280 | G | A | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+375G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71149280 | |||||||
chrX:71149688 | G | A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0102 others(9): Show |
13 | HG02165.hp1 HG02523.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.517+783G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71149688 | |||||||
chrX:71150117 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+1212G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150117 | |||||||
chrX:71150394 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
165 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(162): Show |
intron_variant | MODIFIER | c.517+1489G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150394 | |||||||
chrX:71150439 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.517+1534C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150439 | |||||||
chrX:71150484 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01884.hp2 HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.517+1579G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150484 | |||||||
chrX:71150486 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.517+1581G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150486 | |||||||
chrX:71150561 | G | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0034 others(36): Show |
47 | HG00741.hp1 HG01123.hp1 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.517+1656G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150561 | |||||||
chrX:71150701 | CA | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0068 a0001c0001t0001g0075 others(8): Show |
12 | HG00099.hp1 HG00738.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+1817delA | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 71150701 | ||||||
chrX:71150713 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+1812_517+1821d others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 71150713 | ||||||
chrX:71150718 | A | AG | 3 | a0001c0001t0001g0107 a0001c0001t0002g0115 a0002c0008t0001g0118 |
3 | HG01884.hp2 HG02257.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517+1813_517+1814i others(3): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150718 | |||||||
chrX:71150718 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
140 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.517+1813A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150718 | |||||||
chrX:71150864 | G | A | 2 | a0001c0001t0004g0031 a0001c0001t0004g0164 |
3 | NA18945.hp1 NA18953.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.517+1959G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71150864 | |||||||
chrX:71150893 | A | ATTG | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517+1992_517+1994d others(5): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 71150893 | ||||||
chrX:71151493 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.518-1984G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71151493 | |||||||
chrX:71151576 | G | T | 1 | a0001c0001t0004g0163 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.518-1901G>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71151576 | |||||||
chrX:71151613 | G | A | 23 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0097 others(20): Show |
23 | HG00735.hp2 HG01081.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.518-1864G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71151613 | |||||||
chrX:71151684 | C | A | 1 | a0001c0001t0003g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.518-1793C>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71151684 | |||||||
chrX:71151720 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.518-1757G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71151720 | |||||||
chrX:71151724 | T | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(109): Show |
146 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(143): Show |
intron_variant | MODIFIER | c.518-1753T>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71151724 | |||||||
chrX:71152259 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.518-1218A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71152259 | |||||||
chrX:71152405 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
163 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.518-1072T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71152405 | |||||||
chrX:71153221 | G | C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-256G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71153221 | |||||||
chrX:71153304 | G | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.518-173G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71153304 | |||||||
chrX:71153366 | C | T | 39 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(36): Show |
50 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.518-111C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 3/7 | chrX | 71153366 | |||||||
chrX:71153558 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.577+22C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153558 | |||||||
chrX:71153588 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0179 others(3): Show |
11 | HG02015.hp1 HG02083.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.577+52C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153588 | |||||||
chrX:71153721 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.577+185A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153721 | |||||||
chrX:71153792 | C | G | 3 | a0001c0001t0002g0132 a0001c0002t0001g0116 a0001c0002t0001g0121 |
3 | HG02615.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.577+256C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153792 | |||||||
chrX:71153858 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.577+322G>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153858 | |||||||
chrX:71153885 | C | T | 1 | a0001c0001t0002g0013 | 3 | HG02922.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.577+349C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153885 | |||||||
chrX:71153894 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.577+358C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71153894 | |||||||
chrX:71154076 | C | A | 4 | a0001c0001t0001g0089 a0001c0001t0002g0132 a0001c0002t0001g0116 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+540C>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154076 | |||||||
chrX:71154319 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.577+783G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154319 | |||||||
chrX:71154354 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(134): Show |
172 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(169): Show |
intron_variant | MODIFIER | c.577+818A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154354 | |||||||
chrX:71154372 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0033 others(9): Show |
17 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.577+836G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154372 | |||||||
chrX:71154743 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.578-471G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154743 | |||||||
chrX:71154767 | G | A | 20 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0001t0002g0002 others(17): Show |
27 | HG00639.hp2 HG01109.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.578-447G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154767 | |||||||
chrX:71154772 | T | A | 1 | a0001c0001t0002g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.578-442T>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71154772 | |||||||
chrX:71155040 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.578-174C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71155040 | |||||||
chrX:71155173 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.578-41G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 4/7 | chrX | 71155173 | |||||||
chrX:71155402 | T | A | 1 | a0001c0001t0002g0128 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.727+39T>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71155402 | |||||||
chrX:71155644 | T | C | 1 | a0001c0001t0005g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727+281T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71155644 | |||||||
chrX:71155799 | C | T | 1 | a0002c0008t0001g0118 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.727+436C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71155799 | |||||||
chrX:71155800 | G | A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0124 a0001c0001t0001g0141 others(22): Show |
28 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.727+437G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71155800 | |||||||
chrX:71155937 | C | G | 3 | a0001c0001t0005g0073 a0001c0001t0005g0074 a0001c0001t0005g0087 |
3 | HG02258.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.727+574C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71155937 | |||||||
chrX:71155968 | G | A | 3 | a0001c0001t0003g0063 a0001c0001t0003g0111 a0001c0001t0003g0123 |
3 | HG01993.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.727+605G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71155968 | |||||||
chrX:71156019 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
138 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.727+656G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156019 | |||||||
chrX:71156321 | C | G | 1 | a0001c0001t0001g0024 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.727+958C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156321 | |||||||
chrX:71156342 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.727+979T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156342 | |||||||
chrX:71156360 | A | G | 1 | a0001c0002t0001g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.727+997A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156360 | |||||||
chrX:71156516 | G | A | 19 | a0001c0001t0002g0025 a0001c0001t0002g0029 a0001c0001t0002g0085 others(16): Show |
21 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.727+1153G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156516 | |||||||
chrX:71156540 | A | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0081 others(44): Show |
66 | HG00639.hp2 HG00673.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.727+1177A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156540 | |||||||
chrX:71156687 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.727+1324C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71156687 | |||||||
chrX:71157134 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.727+1771G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71157134 | |||||||
chrX:71157287 | C | CTTAT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(79): Show |
113 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.727+1958_727+1961d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71157287 | ||||||
chrX:71157287 | C | CTTATTTA others(1): Show |
19 | a0001c0001t0001g0015 a0001c0001t0001g0120 a0001c0001t0001g0133 others(16): Show |
23 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.727+1954_727+1961d others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71157287 | ||||||
chrX:71157287 | C | CTTATTTA others(5): Show |
3 | a0001c0001t0002g0096 a0001c0001t0002g0144 a0001c0001t0002g0177 |
3 | HG02922.hp2 HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.727+1950_727+1961d others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71157287 | ||||||
chrX:71157287 | CTTAT | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0086 others(10): Show |
14 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.727+1958_727+1961d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71157287 | ||||||
chrX:71157287 | CTTATTTA others(1): Show |
C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.727+1954_727+1961d others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71157287 | ||||||
chrX:71157287 | CTTATTTA others(5): Show |
C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0043 |
4 | HG00735.hp1 HG01074.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1950_727+1961d others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71157287 | ||||||
chrX:71157363 | G | A | 23 | a0001c0001t0002g0025 a0001c0001t0002g0029 a0001c0001t0002g0069 others(20): Show |
25 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.727+2000G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71157363 | |||||||
chrX:71157819 | G | A | 17 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(14): Show |
17 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.727+2456G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71157819 | |||||||
chrX:71157862 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.727+2499G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71157862 | |||||||
chrX:71158015 | A | T | 6 | a0001c0001t0001g0086 a0001c0001t0002g0132 a0001c0002t0001g0084 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+2652A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158015 | |||||||
chrX:71158062 | TTTAA | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0043 others(1): Show |
5 | HG00735.hp1 HG01074.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.727+2726_727+2729d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71158062 | ||||||
chrX:71158154 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.727+2791C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158154 | |||||||
chrX:71158381 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.727+3018G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158381 | |||||||
chrX:71158679 | T | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(116): Show |
153 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.727+3316T>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158679 | |||||||
chrX:71158804 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0178 a0001c0006t0001g0019 |
3 | HG02523.hp1 NA18990.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.727+3441T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158804 | |||||||
chrX:71158849 | C | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
7 | NA18940.hp1 NA18955.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+3486C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158849 | |||||||
chrX:71158879 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG00323.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.727+3516A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158879 | |||||||
chrX:71158995 | C | T | 42 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0013 others(39): Show |
58 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.727+3632C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71158995 | |||||||
chrX:71159011 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(116): Show |
153 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.727+3648T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159011 | |||||||
chrX:71159019 | C | T | 1 | a0001c0007t0002g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.727+3656C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159019 | |||||||
chrX:71159329 | A | G | 6 | a0001c0001t0001g0086 a0001c0001t0002g0132 a0001c0002t0001g0084 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+3966A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159329 | |||||||
chrX:71159629 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.727+4266C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159629 | |||||||
chrX:71159683 | T | G | 1 | a0001c0001t0002g0160 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.727+4320T>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159683 | |||||||
chrX:71159726 | C | CT | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(115): Show |
151 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.727+4375dupT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71159726 | ||||||
chrX:71159776 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.728-4367G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159776 | |||||||
chrX:71159890 | A | AT | 20 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0036 others(17): Show |
25 | HG00621.hp1 HG00735.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.728-4229dupT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71159890 | ||||||
chrX:71159890 | A | ATT | 7 | a0001c0001t0001g0043 a0001c0001t0002g0029 a0001c0001t0002g0110 others(4): Show |
8 | HG01081.hp1 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.728-4230_728-4229d others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71159890 | ||||||
chrX:71159890 | AT | A | 56 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0050 others(53): Show |
71 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.728-4229delT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71159890 | ||||||
chrX:71159964 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.728-4179G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71159964 | |||||||
chrX:71160028 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(116): Show |
153 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.728-4115A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160028 | |||||||
chrX:71160031 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02080.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.728-4112C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160031 | |||||||
chrX:71160213 | C | CT | 28 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0099 others(25): Show |
30 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.728-3915dupT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71160213 | ||||||
chrX:71160217 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0112 |
3 | HG02895.hp1 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.728-3926T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160217 | |||||||
chrX:71160218 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.728-3925T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160218 | |||||||
chrX:71160266 | G | C | 8 | a0001c0001t0002g0027 a0001c0001t0002g0079 a0001c0001t0002g0100 others(5): Show |
9 | HG01123.hp1 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.728-3877G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160266 | |||||||
chrX:71160468 | C | T | 3 | a0001c0001t0003g0005 a0001c0001t0003g0155 a0001c0001t0003g0156 |
7 | HG01884.hp1 HG02145.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-3675C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160468 | |||||||
chrX:71160907 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-3236T>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71160907 | |||||||
chrX:71161115 | CT | C | 66 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0042 others(63): Show |
85 | HG00639.hp2 HG00673.hp1 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.728-3012delT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71161115 | ||||||
chrX:71161361 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.728-2782G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71161361 | |||||||
chrX:71161706 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.728-2437G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71161706 | |||||||
chrX:71161842 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
10 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-2301G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71161842 | |||||||
chrX:71161970 | T | C | 18 | a0001c0001t0002g0025 a0001c0001t0002g0029 a0001c0001t0002g0092 others(15): Show |
20 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.728-2173T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71161970 | |||||||
chrX:71162116 | AT | A | 10 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0133 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.728-2015delT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 71162116 | ||||||
chrX:71162314 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.728-1829G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71162314 | |||||||
chrX:71162332 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.728-1811A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71162332 | |||||||
chrX:71162425 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
149 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(146): Show |
intron_variant | MODIFIER | c.728-1718T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71162425 | |||||||
chrX:71162608 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.728-1535G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71162608 | |||||||
chrX:71162793 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.728-1350C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71162793 | |||||||
chrX:71162983 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.728-1160A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71162983 | |||||||
chrX:71163462 | G | A | 1 | a0001c0001t0009g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.728-681G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71163462 | |||||||
chrX:71163594 | T | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(113): Show |
150 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(147): Show |
intron_variant | MODIFIER | c.728-549T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71163594 | |||||||
chrX:71163818 | A | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.728-325A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71163818 | |||||||
chrX:71163977 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.728-166G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71163977 | |||||||
chrX:71164080 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.728-63C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 5/7 | chrX | 71164080 | |||||||
chrX:71164416 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.913+88T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71164416 | |||||||
chrX:71164417 | C | T | 84 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(81): Show |
102 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.913+89C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71164417 | |||||||
chrX:71164499 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.913+171A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71164499 | |||||||
chrX:71164651 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(22): Show |
40 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.913+323T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71164651 | |||||||
chrX:71164836 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.913+508A>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71164836 | |||||||
chrX:71165225 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.913+897C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71165225 | |||||||
chrX:71165381 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.913+1053C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71165381 | |||||||
chrX:71165497 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.913+1169G>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71165497 | |||||||
chrX:71165556 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
149 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(146): Show |
intron_variant | MODIFIER | c.913+1228T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71165556 | |||||||
chrX:71165583 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.913+1255G>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71165583 | |||||||
chrX:71165905 | A | G | 1 | a0001c0001t0008g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.914-1106A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71165905 | |||||||
chrX:71166055 | C | CT | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0097 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-945dupT | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 71166055 | ||||||
chrX:71166170 | G | T | 1 | a0001c0001t0008g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.914-841G>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166170 | |||||||
chrX:71166171 | T | C | 1 | a0001c0001t0008g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.914-840T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166171 | |||||||
chrX:71166226 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.914-785G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166226 | |||||||
chrX:71166324 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.914-687C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166324 | |||||||
chrX:71166378 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.914-633C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166378 | |||||||
chrX:71166404 | C | T | 6 | a0001c0001t0001g0086 a0001c0001t0002g0132 a0001c0002t0001g0084 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-607C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166404 | |||||||
chrX:71166457 | CA | C | 75 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0174 others(72): Show |
93 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.914-539delA | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 71166457 | ||||||
chrX:71166457 | CAA | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.914-540_914-539del others(2): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 71166457 | ||||||
chrX:71166622 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.914-389C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166622 | |||||||
chrX:71166975 | C | G | 1 | a0001c0001t0003g0063 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.914-36C>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 6/7 | chrX | 71166975 | |||||||
chrX:71167817 | G | T | 1 | a0001c0001t0008g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1703+17G>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71167817 | |||||||
chrX:71167818 | T | G | 1 | a0001c0001t0008g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1703+18T>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71167818 | |||||||
chrX:71168082 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1703+282C>T | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168082 | |||||||
chrX:71168206 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1703+406G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168206 | |||||||
chrX:71168363 | T | C | 20 | a0001c0001t0002g0025 a0001c0001t0002g0029 a0001c0001t0002g0069 others(17): Show |
22 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1703+563T>C | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168363 | |||||||
chrX:71168615 | C | A | 1 | a0001c0001t0008g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1704-639C>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168615 | |||||||
chrX:71168705 | G | A | 23 | a0001c0001t0002g0025 a0001c0001t0002g0029 a0001c0001t0002g0069 others(20): Show |
25 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1704-549G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168705 | |||||||
chrX:71168747 | GAGAA | G | 4 | a0001c0001t0003g0005 a0001c0001t0003g0091 a0001c0001t0003g0155 others(1): Show |
8 | HG01255.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1704-499_1704-496d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168747 | ||||||
chrX:71168792 | A | G | 83 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0071 others(80): Show |
102 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1704-462A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168792 | |||||||
chrX:71168798 | G | A | 83 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0071 others(80): Show |
102 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1704-456G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168798 | |||||||
chrX:71168814 | GA | G | 29 | a0001c0001t0001g0099 a0001c0001t0002g0002 a0001c0001t0002g0013 others(26): Show |
36 | HG01109.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.1704-430delA | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168814 | ||||||
chrX:71168820 | AAAAAGAA others(6): Show |
A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0005g0073 others(2): Show |
5 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1704-430_1704-418d others(15): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168820 | ||||||
chrX:71168820 | AAAAAGAA others(10): Show |
A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0154 |
2 | HG00738.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1704-430_1704-414d others(19): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168820 | ||||||
chrX:71168821 | A | AAAAG | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
38 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1704-387_1704-384d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAAAGAAA others(1): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
25 | HG00733.hp1 HG00735.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1704-391_1704-384d others(10): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAAAGAAA others(5): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0022 others(7): Show |
12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1704-395_1704-384d others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAAG | 27 | a0001c0001t0001g0134 a0001c0001t0001g0153 a0001c0001t0002g0012 others(24): Show |
29 | HG00673.hp1 HG00735.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1704-431_1704-430i others(5): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAAGAAAG | 6 | a0001c0001t0001g0024 a0001c0001t0002g0014 a0001c0001t0002g0144 others(3): Show |
8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1704-431_1704-430i others(9): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAAGAAAG others(4): Show |
3 | a0001c0001t0002g0025 a0001c0001t0002g0100 a0001c0001t0005g0138 |
3 | HG01243.hp1 HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1704-431_1704-430i others(13): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAGAAAGA others(3): Show |
2 | a0001c0001t0002g0146 a0001c0002t0001g0130 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1704-432_1704-431i others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AAGAAAGA others(11): Show |
1 | a0001c0001t0002g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1704-432_1704-431i others(20): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | A | AGAAAGAA others(6): Show |
1 | a0001c0001t0002g0030 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1704-433_1704-432i others(15): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168821 | |||||||
chrX:71168821 | A | G | 5 | a0001c0001t0002g0027 a0001c0001t0002g0173 a0001c0001t0003g0005 others(2): Show |
5 | HG01978.hp1 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1704-433A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168821 | |||||||
chrX:71168821 | AAAAG | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(21): Show |
37 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1704-387_1704-384d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168821 | AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0002g0145 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1704-403_1704-384d others(22): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168821 | ||||||
chrX:71168823 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1704-431A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168823 | |||||||
chrX:71168826 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1704-428A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168826 | |||||||
chrX:71168828 | AGAAAGAA others(6): Show |
A | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1704-425_1704-413d others(15): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168828 | |||||||
chrX:71168845 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1704-409G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168845 | |||||||
chrX:71168855 | AAG | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0062 |
6 | NA18940.hp1 NA18955.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1704-397_1704-396d others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168855 | ||||||
chrX:71168856 | AGAAAGAA others(21): Show |
A | 1 | a0001c0001t0005g0087 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1704-397_1704-370d others(30): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168856 | |||||||
chrX:71168859 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0003g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1704-385_1704-376d others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168859 | ||||||
chrX:71168867 | AAG | A | 18 | a0001c0001t0001g0099 a0001c0001t0002g0002 a0001c0001t0002g0013 others(15): Show |
18 | HG01256.hp1 HG01891.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.1704-383_1704-382d others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168867 | ||||||
chrX:71168869 | G | GAA | 59 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0134 others(56): Show |
72 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1704-384_1704-383i others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168869 | ||||||
chrX:71168869 | G | GAAAGAAA others(3): Show |
2 | a0001c0001t0002g0012 a0001c0001t0003g0005 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1704-384_1704-383i others(12): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168869 | ||||||
chrX:71168869 | GAGAA | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0075 others(1): Show |
4 | HG02572.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1704-379_1704-376d others(6): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168869 | ||||||
chrX:71168869 | GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0002g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1704-383_1704-372d others(14): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168869 | ||||||
chrX:71168875 | GA | G | 18 | a0001c0001t0001g0153 a0001c0001t0002g0002 a0001c0001t0002g0054 others(15): Show |
23 | HG00673.hp1 HG01109.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1704-375delA | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168875 | ||||||
chrX:71168876 | A | AAAG | 12 | a0001c0001t0001g0134 a0001c0001t0002g0014 a0001c0001t0002g0094 others(9): Show |
14 | HG00639.hp2 HG01081.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1704-376_1704-375i others(5): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168876 | ||||||
chrX:71168879 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0005g0138 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1704-375A>G | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168879 | |||||||
chrX:71168882 | AAG | A | 49 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0071 others(46): Show |
60 | HG00735.hp2 HG01123.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.1704-368_1704-367d others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168882 | ||||||
chrX:71168883 | AG | A | 20 | a0001c0001t0001g0134 a0001c0001t0001g0153 a0001c0001t0002g0002 others(17): Show |
25 | HG00673.hp1 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1704-370delG | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168883 | |||||||
chrX:71168884 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1704-370G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168884 | |||||||
chrX:71168884 | G | GAA | 3 | a0001c0001t0002g0100 a0001c0001t0002g0147 a0001c0001t0005g0138 |
3 | HG02109.hp2 HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1704-369_1704-368i others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168884 | ||||||
chrX:71168884 | G | GAAA | 4 | a0001c0001t0002g0014 a0001c0001t0002g0161 a0001c0001t0002g0168 others(1): Show |
5 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704-369_1704-368i others(5): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168884 | ||||||
chrX:71168884 | G | GAAAAGAA | 5 | a0001c0001t0002g0094 a0001c0001t0002g0128 a0001c0001t0002g0148 others(2): Show |
5 | HG01081.hp1 HG02145.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1704-369_1704-368i others(9): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168884 | ||||||
chrX:71168884 | G | GAAAGAA | 2 | a0001c0001t0002g0030 a0001c0001t0002g0112 |
3 | HG02895.hp1 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1704-369_1704-368i others(8): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168884 | ||||||
chrX:71168896 | AAG | A | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1704-356_1704-355d others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168896 | ||||||
chrX:71168898 | G | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0112 |
3 | HG02895.hp1 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1704-356G>A | NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | chrX | 71168898 | |||||||
chrX:71168898 | G | GAA | 3 | a0001c0001t0001g0134 a0001c0001t0001g0153 a0001c0001t0005g0087 |
3 | HG02886.hp2 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1704-354_1704-353d others(4): Show |
NLGN3 | ENSG00000196338.15 | transcript | ENST00000358741.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 71168898 |